Join the 200th Anniversary Celebration

Original Article

The Elimination of Indigenous Measles, Mumps, and Rubella from Finland by a 12-Year, Two-Dose Vaccination Program

Heikki Peltola, Olli P. Heinonen, Martti Valle, Mikko Paunio, Martti Virtanen, Viena Karanko, and Kari Cantell

N Engl J Med 1994; 331:1397-1402November 24, 1994

Abstract

Background

In the 1970s measles, mumps, and rubella were rampant in Finland, and rates of immunization were inadequate. In 1982 a comprehensive national vaccination program began in which two doses of a combined live-virus vaccine were used.

Methods

Public health nurses at 1036 child health centers administered the vaccine to children at 14 to 18 months of age and again at 6 years, and also to selected groups of older children and young adults. Vaccination was voluntary and free of charge. In follow-up studies, we focused on rates of vaccination, reasons for noncompliance, adverse reactions, immunogenicity, persistence of antibody, and incidence of the three diseases. Since 1987, paired serum samples have been collected from all patients with suspected cases of measles, mumps, or rubella.

Results

Over a period of 12 years, 1.5 million of the 5 million people in Finland were vaccinated. Coverage now exceeds 95 percent. The vaccine was efficient and safe, even in those with a history of severe allergy. No deaths or persistent sequelae were attributable to vaccination. The most frequent complication requiring hospitalization was acute thrombocytopenic purpura, which occurred at a rate of 3.3 per 100,000 vaccinated persons. The 99 percent decrease in the incidence of the three diseases was accompanied by an increasing rate of false positive clinical diagnoses. In 655 vaccinated patients with clinically diagnosed disease, serologic studies confirmed the presence of measles in only 0.8 percent, mumps in 2.0 percent, and rubella in 1.2 percent. The few localized outbreaks were confined to patients in the partially vaccinated age groups. There are now fewer than 30 sporadic cases of each of the three diseases per year, and those are probably imported.

Conclusions

Over a 12-year period, an immunization program using two doses of combined live-virus vaccine has eliminated indigenous measles, mumps, and rubella from Finland. Serologic studies show that most reported sporadic cases are now due to other causes, but a continued high rate of vaccination coverage is essential to prevent outbreaks resulting from exposure to imported disease.

Media in This Article

Figure 1Annual Number of Cases of Measles, Mumps, and Rubella in Finland.
Figure 2Distribution of Cases during Outbreaks of Measles, Mumps, and Rubella.
Article

In Finland in the 1970s, the mean annual incidence of measles was 366 per 100,000, that of mumps was 240 per 100,000, and that of rubella was 104 per 100,000. In the Finnish population of 5 million, large epidemics caused hundreds of hospitalizations and about 100 cases of encephalitis each year1. A live-virus measles vaccine was introduced in 1975; because only 70 percent of the target population was vaccinated,2 however, the disease was not eliminated3,4. Mumps once occurred in 20 to 30 percent of military conscripts. Meningitis and orchitis were common sequelae, and there were even occasional deaths5. Hearing impairment occurred in 4 percent of the cases and was permanent in 5 of every 100,0006. An inactivated-virus mumps vaccine was developed and routinely administered by the military as early as 1960, but vaccination was not extended to the civilian population despite the 900 hospitalizations per year, frequent hearing loss, and chronic encephalomyelitis7. Rubella can cause chronic arthritis in childhood and can result in hearing impairment8-10. In Finland there were 40 to 50 cases of rubella embryopathy each year. A live-virus rubella vaccine was introduced for use in young girls in 1975.

In 1982 a combined live-virus measles-mumps-rubella (MMR) vaccine was approved, and a comprehensive immunization program was launched to eliminate indigenous cases of the three diseases from Finland by vaccinating children twice. We determined rates of vaccination, adverse reactions, incidence of disease, and other epidemiologic variables during the course of the program. As we indicate in this report, the goal of the program has been achieved.

Methods

The only MMR vaccine used in Finland during the study period was a live-virus vaccine (M-M-R II or Virivac, Merck, Sharp & Dohme, Rahway, N.J.) consisting of the Moraten (Enders-Edmonston B) strain of measles virus, the Jeryl Lynn B strain of mumps virus, and the Wistar RA 27/3 strain of rubella virus. The vaccine dose of 0.5 ml contained 25 μg of neomycin and less than 20 μg of phenol red indicator. It was injected subcutaneously into the upper arm or buttock.

Children 14 to 18 months and 6 years of age were vaccinated beginning in November 1982. In order to accelerate the immunization program, children who were between 18 months and 6 years old in November 1982 were vaccinated in 1983 through 1986. The program was later extended to military conscripts, children 11 to 13 years old, mothers who were seronegative for rubella after delivery, and students at various schools of nursing.

All childhood vaccinations were voluntary, free of charge, and performed by nurses after oral consent was obtained from parents.

As described in detail elsewhere,2 the MMR vaccination program took place under the auspices of the National Board of Health and was organized by the National Public Health Institute in Helsinki. Briefly, Finland is divided into 1036 child health areas, each of which is covered by a child health center run by a physician and public health nurses. The nurses were trained in the program procedures by means of local teaching seminars and printed material.

Follow-up Studies

Special forms and instructions were designed for several substudies, which focused on vaccination rates,2 common adverse reactions to the vaccine,11 and tolerability of the vaccine in those with a history of severe allergy12. Arrangements were made to identify the unvaccinated children13 and to detect any complications too rare for detection by a controlled trial in 1162 twins11. Serologic confirmation was undertaken for suspected cases of disease. Every vaccinated person was identified by social security number. Unvaccinated children were identified by linkage of health center records with the national population register. In surveillance for rare adverse events, true complications were defined as those considered life-threatening (for example, anaphylaxis) and those that resulted in hospitalization or permanent sequelae.

Serum was obtained from a sample of 300 children from three areas at intervals of one to three years in order to monitor antibody levels. Measles antibodies were measured by the classic hemagglutination-inhibition technique,14 with antibody titers of 1:20 or higher considered protective. Rubella antibodies were determined with the hemolysis-in-gel technique15 (Orivir Rubella, Orion Diagnostica, Espoo, Finland). An area of hemolysis with a diameter of 6 mm or more was considered to indicate clinical protection. Measurement of mumps antibodies was performed by enzyme immunoassay and the plaque-inhibition technique16.

During the first five years of the study the incidence of the three diseases was monitored by clinical reports. In 1987 virologic confirmation was required for all suspected cases. Tubes for the collection of paired serum samples with prepaid mailing envelopes were distributed to child health centers.

Vaccination Coverage

The target population of the program was 563,000 children, of whom 86 percent were vaccinated in 1982 through 1986. A special campaign was then undertaken,13 beginning with reports in the national media and the local newspapers. Lists of unvaccinated children were then sent to the public health nurses, who personally contacted the parents. Finally, personal letters were sent to the nonparticipating families. These efforts resulted in the vaccination of 62,000 additional children, increasing participation to 97 percent. The hard-to-reach group was characterized by a survey and has since received special attention.

Results

Vaccine Reactions and Complications

A large double-blind crossover trial in twins showed only a few relatively common adverse reactions attributable to the MMR vaccine11. In all, local or systemic reactions were observed in 4 to 5 percent of the vaccinated children. Our findings challenge those of previous uncontrolled studies (Table 1Table 1Symptoms and Signs Attributed to the MMR Vaccine in Five Studies.) that reported much higher rates of reactions17-19. In one double-blind, placebo-controlled study,20 the incidence of respiratory symptoms was virtually identical among the vaccinated and unvaccinated groups (72 and 74 percent, respectively).

In all, 1.5 million children and young adults, about a third of the Finnish population, were immunized in 1982 through 1993. No deaths or permanent sequelae were reported. There were more reports of rare complications early in the study than later, despite the use of the same surveillance system. Febrile convulsions attributable to vaccination had an incidence of approximately 7 per 100,000 vaccinated children, and 5 children had urticaria (0.6 per 100,000). Several children received epinephrine because of a suspected general allergic reaction; only two had probable vaccination anaphylaxis, and both recovered uneventfully. Diabetes was diagnosed in one child two weeks after vaccination, which is less than the expected incidence21. A girl who had earlier received a measles vaccine (Schwarz strain) was immunized with the MMR vaccine at seven years of age, and acute lymphatic leukemia was diagnosed 23 days later. Severe encephalopathy developed, and measles virus was isolated from the cerebrospinal fluid on two occasions. She recovered uneventfully22.

The most common complication clearly attributable to the MMR vaccine was acute thrombocytopenic purpura, detected in 23 children23. The estimated incidence was 3.3 cases per 100,000 vaccinated children. Characteristically, petechiae or ecchymosis developed within 3 weeks after vaccination (median, 17 days). Circulating antiplatelet autoantibodies suggesting an autoimmune mechanism were found in 33 percent of the patients. Full recovery within six months with or without intravenous immune globulin therapy was the rule.

The vaccine was well tolerated even by those with a history of severe allergy; only 7 of 135 severely allergic children were not vaccinated because of a positive reaction to the MMR vaccine on a skin-prick test12.

Serologic Findings

The measles component of the vaccine induced seroconversion in 99 percent of the 159 seronegative children from whom paired serum samples were available. The single exception was a girl who responded adequately to the rubella and mumps antigens. For the rubella component, the rate of seroconversion in 167 previously seronegative children was 100 percent. The antibody response to the mumps component of the vaccine was less clear because of the lack of a suitable laboratory method of assessing seroconversion. Antibodies were detected one year after vaccination in 94 percent of 170 previously seronegative children; this finding suggests that good protection was induced.

The measles and rubella antibodies persisted at high levels for at least four years after vaccination, and few children did not have protective levels of antibodies. The second dose of the vaccine given to children at six years of age also induced a good response against all three components, with the highest antibody levels against rubella and mumps (data not shown). The slightly weaker response to the measles-virus component (data not shown) might be explained by the very high antibody concentrations prevalent before the second dose was given, since the greatest response occurred among the children who had the lowest antibody levels after the first dose.

Clinical versus Virologic Diagnosis

Clinical suspicion of measles, mumps, or rubella was rarely confirmed serologically after the program had been in effect for several years. In a series of 655 consecutive vaccinated children in whom one of the three diseases was clinically diagnosed through 1986, measles was confirmed serologically in only 0.8 percent (5 cases), mumps in 2.0 percent (13 cases), and rubella in 1.2 percent (8 cases).

Incidence and Outbreaks

The vaccination program has had a substantial effect on the incidence of the three diseases. The lowest number of reported clinical cases of measles was 344 in 1985 (Figure 1Figure 1Annual Number of Cases of Measles, Mumps, and Rubella in Finland.). This implies a reduction of 87 percent from the five-year period before the vaccination program began (1977 through 1981) when there were, on average, 2704 cases reported per year. Actual protection rates were much higher, since unvaccinated age groups were also included in the reports. Serologic data indicate a decline from 317 new cases of measles in 1987 to 13 in 1993 (Figure 1).

Small outbreaks of measles occurred in different regions, almost exclusively among the unvaccinated age groups. Often the index patient in such outbreaks had recently traveled abroad. Each year about 1 million Finns, one fifth of the population, visit another country. In an outbreak in 1988 and 1989, when there were 1748 confirmed cases of measles, there were far fewer among the 2-to-12-year-olds then covered by the program than among the unvaccinated older children (Figure 2Figure 2Distribution of Cases during Outbreaks of Measles, Mumps, and Rubella.).

Verified cases of mumps declined to less than 20 per year in 1990 through 1993 (Figure 1) -- a decrease of more than 99 percent from the average of 9366 cases per year in 1977 through 1981. A local outbreak of 77 proved cases occurred in central Finland in 1987 and 1988 (Figure 2). Again, these cases occurred almost exclusively in the unvaccinated age groups. The changing epidemiologic features of mumps were reflected clinically in the fact that the most common form of encephalitis, that caused by the mumps virus, disappeared from the country1.

The difficulty of making the diagnosis of rubella on clinical grounds renders traditional reporting unreliable. Nevertheless, no vaccinated patient was found among 423 with laboratory-confirmed rubella in 1984 through 1986, including some children too old (11 years or more) to have been vaccinated during the program24. The lowest number of rubella cases was in 1993, when there were 25 documented cases overall (Figure 1). The efficacy of the vaccine in a rubella outbreak is indicated by the age distribution of the 336 cases confirmed in 1991 (Figure 2).

Discussion

In slightly more than a decade a program of vaccination against measles, mumps, and rubella virtually eliminated these diseases from Finland. Careful planning, efficient organization, and an effective system of primary health care for children ensured high rates of vaccination coverage throughout the country. The two-dose vaccination policy was an important factor in the program's sustained success. The rationale for this policy was threefold. First, up to 5 percent of recipients were expected to have no response to all three vaccine components (primary failures)25. Second, a two-dose regimen was considered likely to reach more children than a single-dose schedule. Finally, the second dose was expected to boost declining antibody concentrations.

The decision to immunize children at 14 to 18 months and 6 years of age was made for several reasons. There was no reason for initiating immunization with the MMR vaccine before the first birthday, as there is in developing countries26. The system of primary health care for children required a visit to the center after the first birthday, when no other immunization was scheduled. Because most Finnish children enter school at seven years of age, the second dose was received before school entry, thus avoiding the need to involve the school health system in the program. The two-dose vaccination policy generated higher costs than a single-dose policy but had the advantage of compensating for more violations of the vaccination schedule.

The vaccine proved to be safe. For common adverse reactions (occurring within 21 days after vaccination), the data could hardly be more reliable than those from the double-blind, placebo-controlled crossover study performed in more than 1000 twins11. In that study, the great majority of symptoms and signs earlier attributed to the vaccine were found to have other causes. The incidence of adverse reactions was substantially lower among these children than among children in four studies, three of which were uncontrolled (Table 1). Except for mild arthralgia in about 1 percent of those vaccinated,11 arthropathy or other adverse effects have not occurred, perhaps because we were immunizing children rather than adults, in whom acute arthritis more often develops27.

Among rare adverse reactions, nationwide surveillance revealed that acute thrombocytopenic purpura, clinically indistinguishable from childhood idiopathic thrombocytopenic purpura, was the most common true complication of the MMR vaccine. This is not surprising, since low platelet counts also occur after natural cases of measles,28 mumps,29 and especially rubella30,31. Moreover, thrombocytopenia has been described after vaccinations against measles32 and rubella,33 although the incidence was lower than that following natural infection30. In our program, no permanent sequelae of post-vaccination thrombocytopenia have been reported23. Mumps-vaccine-related meningitis is rare34.

A small, slow decline in antibody levels occurred after the first dose of the vaccine. Although a loss of antibodies to levels below the detection limit of available assays does not necessarily imply the loss of clinical protection,16 it is plausible that boosted levels predict long-lasting protection35.

Only 0.8 percent of the clinically diagnosed cases of measles were verifiable serologically, and the disease gradually disappeared from Finland. When measles was still rampant, cases of measles-like diseases (whose incidence may not have changed much since the vaccination program) represented a tiny fraction of the true measles cases. Now the ratio of measles-mimicking diseases to true measles is dramatically higher. Hence, the true clinical efficacy of the MMR vaccine is far greater than it appears to be when cases without serologic confirmation are included. This difference in apparent incidence prompted a new approach after five years of the program. From 1987 on, only virologically proved cases of measles, mumps, or rubella were counted. Serologic testing, which was encouraged and provided free of charge, was the only method of confirming that the true incidence was approaching zero, even if some cases were missed in the process. Our studies in progress indicate that many suspected cases of these three diseases were in fact caused by other viruses. A reduction of more than 90 percent in the incidence of all three diseases occurred within a few years, as had been expected on the basis of vaccination programs in the United States36 and Sweden18. Further declines to almost zero occurred over the 12 years of the program.

In Finland, the use of the MMR vaccine has wiped out one third of all childhood encephalitis, of which 16, 13, and 2 percent of the cases were once caused by the mumps, measles, and rubella viruses, respectively1. The rising incidence of type 1 diabetes, especially among five-to-nine-year-old children, has reached a plateau,37 a fact that may be due to the vaccination program. Vaccination against rubella is undertaken to eliminate the associated embryopathy. Declining numbers of verified cases of rubella (Figure 1), with no vaccinated persons among 423 with proved cases in 1986,24 indicate that the MMR vaccine is successful in preventing this disease.

Maintaining good immunity in the population is the cornerstone of the control of epidemics of measles, mumps, and rubella. In Finland, where the primary health care system is well organized and efficient and the two-dose vaccination regimen is routine, it is feasible to immunize the population with a further dose, should the need arise. In 1987 and 1988, a mumps outbreak (Figure 2) was successfully extinguished by the immunization of 500 previously unvaccinated schoolchildren.

In the United States, where, in addition to the vaccine failures in young adults, many cases of measles occur in preschool children, those living in the inner city, those who are indigent, and unimmunized infants,38 the recommended 70 to 90 percent vaccination coverage39,40 is generally not achieved before school age41. A second dose is likely to prevent primary and secondary vaccine failures,42 and in fact, this policy was adopted in 1989 in the United States and in 1991 in New Zealand43; it is under discussion in Japan40 and the United Kingdom44. However, a two-dose policy alone does not guarantee the protection of young children if vaccination is not ensured before the age of school entry41. A policy such as ours, which includes tracing unvaccinated children, has proved effective, feasible, and cost effective,13 and such a policy might be adopted in the United States41. Hong Kong, on the other hand, has chosen another strategy45. Every contact of a child with the health care system is regarded as an opportunity for immunization; this policy has increased vaccination rates to 97 percent. The same strategy is now being used in the United States46.

In Finland, the annual number of cases of measles, mumps, and rubella has been reduced to a few dozen, and the circulation of the three viruses has been interrupted. Indigenous cases of measles, mumps, and rubella have been virtually eliminated. Since international tourism continues to lead to the importation of these viruses, however, it is necessary to maintain high rates of vaccination coverage if future epidemics are to be prevented.

Source Information

From the National Public Health Institute (H.P., O.P.H., M.Valle, M.P., M.Virtanen, V.K., K.C.); the Division of Infectious Diseases, Children's Hospital, University of Helsinki (H.P., M.Virtanen, V.K.); and the Department of Public Health, University of Helsinki (O.P.H., M.P.) -- all in Helsinki, Finland.

Address reprint requests to Dr. Peltola at Children's Hospital, University of Helsinki, 11 Stenback St., FIN-00290 Helsinki, Finland.

References

References

  1. 1

    Koskiniemi M, Vaheri A. Effect of measles, mumps, rubella vaccination on pattern of encephalitis in children. Lancet 1989;1:31-34
    CrossRef | Web of Science | Medline

  2. 2

    Peltola H, Karanko V, Kurki T, et al. Rapid effect on endemic measles, mumps, and rubella of nationwide vaccination programme in Finland. Lancet 1986;1:137-139
    CrossRef | Web of Science | Medline

  3. 3

    Anderson RM, May RM. Vaccination against rubella and measles: quantitative investigations of different policies. J Hyg (Lond) 1983;90:259-325
    CrossRef | Web of Science | Medline

  4. 4

    Hethcote HW. Measles and rubella in the United States. Am J Epidemiol 1983;117:2-13
    Web of Science | Medline

  5. 5

    Penttinen K, Cantell K, Somer P, Poikolainen A. Mumps vaccination in the Finnish Defense Forces. Am J Epidemiol 1968;88:234-244
    Web of Science | Medline

  6. 6

    Vuori M, Lahikainen EA, Peltonen T. Perceptive deafness in connection with mumps: a study of 298 servicemen suffering from mumps. Acta Otolaryngol (Stockh) 1962;55:231-236
    CrossRef | Medline

  7. 7

    Vaheri A, Julkunen I, Koskiniemi M-L. Chronic encephalomyelitis with specific increase in intrathecal mumps antibodies. Lancet 1982;2:685-688
    CrossRef | Web of Science | Medline

  8. 8

    Heinonen OP, Slone D, Shapiro S. Birth defects and drugs in pregnancy. Littleton, Mass.: Publishing Sciences Group, 1977:7-8, 89-91, 121-3, 137-8, 197.

  9. 9

    Chantler JK, Tingle AJ, Petty RE. Persistent rubella virus infection associated with chronic arthritis in children. N Engl J Med 1985;313:1117-1123
    Full Text | Web of Science | Medline

  10. 10

    Ueda K, Tokugawa K, Nishida Y, Kimura M. Incidence of congenital rubella syndrome in Japan (1965-1985): a nationwide survey of the number of deaf children with history of maternal rubella attending special schools for the deaf in Japan. Am J Epidemiol 1986;124:807-815
    Web of Science | Medline

  11. 11

    Peltola H, Heinonen OP. Frequency of true adverse reactions to measles-mumps-rubella vaccine: a double-blind placebo-controlled trial in twins. Lancet 1986;1:939-942
    CrossRef | Web of Science | Medline

  12. 12

    Juntunen-Backman K, Peltola H, Backman A, Salo OP. Safe immunization of allergic children against measles, mumps, and rubella. Am J Dis Child 1987;141:1103-1105
    Web of Science | Medline

  13. 13

    Paunio M, Virtanen M, Peltola H, et al. Increase of vaccination coverage by mass media and individual approach: intensified measles, mumps, and rubella prevention program in Finland. Am J Epidemiol 1991;133:1152-1160
    Web of Science | Medline

  14. 14

    Gershon AA, Krugman S. Measles virus. In: Lennette EH, Schmidt NJ, eds. Diagnostic procedures for viral, rickettsial and chlamydial infections. 5th ed. Washington, D.C.: American Public Health Association, 1979:685-6.

  15. 15

    Vaananen P, Vaheri A. Hemolysis-in-gel test in immunity surveys and diagnosis of rubella. J Med Virol 1979;3:245-252
    CrossRef | Web of Science | Medline

  16. 16

    Weibel RE, Buynak EB, McLean AA, et al. Persistence of antibody in human subjects for 7 to 10 years following administration of combined live attenuated measles, mumps, and rubella virus vaccines. Proc Soc Exp Biol Med 1980;165:260-263
    Web of Science | Medline

  17. 17

    Weibel RE, Carlson AJ Jr, Villarejos VM, Buynak EB, McLean AA, Hilleman MR. Clinical and laboratory studies of combined live measles, mumps, and rubella vaccines using the RA 27/3 rubella virus. Proc Soc Exp Biol Med 1980;165:323-326
    Web of Science | Medline

  18. 18

    Christenson B, Bottiger M, Heller L, et al. Mass vaccination programme aimed at eradicating measles, mumps, and rubella in Sweden: first experience. BMJ 1983;287:389-391
    CrossRef | Web of Science | Medline

  19. 19

    Vesikari T, Ala-Laurila E-L, Heikkinen A, Terho A, D'Hondt E, Andre FE. Clinical trial of a new trivalent measles-mumps-rubella vaccine in young children. Am J Dis Child 1984;138:843-847
    Web of Science | Medline

  20. 20

    Lerman SJ, Bollinger M, Brunken JM. Clinical and serologic evaluation of measles, mumps, and rubella (HPV-77:DE-5 and RA 27/3) virus vaccines, singly and in combination. Pediatrics 1981;68:18-22
    Web of Science | Medline

  21. 21

    Diabetes Epidemiology Research International Group. Geographic patterns of childhood insulin-dependent diabetes mellitus. Diabetes 1988;37:1113-1119
    CrossRef | Web of Science | Medline

  22. 22

    Valmari P, Lanning M, Tuokko H, Kouvalainen K. Measles virus in the cerebrospinal fluid in postvaccination immunosuppressive measles encephalopathy. Pediatr Infect Dis J 1987;6:59-63
    CrossRef | Web of Science | Medline

  23. 23

    Nieminen U, Peltola H, Syrjala MT, Makipernaa A, Kekomaki R. Acute thrombocytopenic purpura following measles, mumps and rubella vaccination: a report on 23 patients. Acta Paediatr 1993;82:267-270
    CrossRef | Web of Science | Medline

  24. 24

    Ukkonen P, von Bonsdorff C-H. Rubella immunity and morbidity: effects of vaccination in Finland. Scand J Infect Dis 1988;20:255-259
    CrossRef | Web of Science | Medline

  25. 25

    Brunell PA, Weigle K, Murphy MD, Shehab Z, Cobb E. Antibody response following measles-mumps-rubella vaccine under conditions of customary use. JAMA 1983;250:1409-1412
    CrossRef | Web of Science | Medline

  26. 26

    Aaby P, Bukh J, Hoff G, et al. High measles mortality in infancy related to intensity of exposure. J Pediatr 1986;109:40-44
    CrossRef | Web of Science | Medline

  27. 27

    Howson CP, Fineberg HV. The ricochet of magic bullets: summary of the Institute of Medicine Report, Adverse Effects of Pertussis and Rubella Vaccines. Pediatrics 1992;89:318-324
    Web of Science | Medline

  28. 28

    Hudson JB, Weinstein L, Chang T-W. Thrombocytopenic purpura in measles. J Pediatr 1956;48:48-56
    CrossRef | Web of Science | Medline

  29. 29

    Graham DY, Brown CH III, Benrey J, Butel JS. Thrombocytopenia: a complication of mumps. JAMA 1974;227:1162-1164
    CrossRef | Web of Science | Medline

  30. 30

    Lokietz H, Reynolds FA. Postrubella thrombocytopenic purpura: report of nine new cases and review of published cases. J Lancet 1965;85:226-230
    Medline

  31. 31

    Bayer WL, Sherman FE, Michaels RH, Szeto ILF, Lewis JH. Purpura in congenital and acquired rubella. N Engl J Med 1965;273:1362-1366
    Full Text | Web of Science | Medline

  32. 32

    Kiefaber RW. Thrombocytopenic purpura after measles vaccination. N Engl J Med 1981;305:225-225
    Web of Science | Medline

  33. 33

    Forrest JM, Honeyman MC, Lovric VA. Rubella vaccination and thrombocytopenia. Aust N Z J Med 1974;4:352-355
    CrossRef | Medline

  34. 34

    Peltola H. Mumps vaccination and meningitis. Lancet 1993;341:994-995
    CrossRef | Web of Science | Medline

  35. 35

    Markowitz LE, Albrecht P, Orenstein WA, Lett SM, Pugliese TJ, Farrell D. Persistence of measles antibody after revaccination. J Infect Dis 1992;166:205-208
    CrossRef | Web of Science | Medline

  36. 36

    Reported vaccine-preventable diseases -- United States, 1993, and the Childhood Immunization Initiative. MMWR Morb Mortal Wkly Rep 1994;43:57-60
    Medline

  37. 37

    Hyoty H, Hiltunen M, Reunanen A, et al. Decline of mumps antibodies in type 1 (insulin-dependent) diabetic children and a plateau in the rising incidence of type 1 diabetes after introduction of the mumps-measles-rubella vaccine in Finland. Diabetologia 1993;36:1303-1308
    CrossRef | Web of Science | Medline

  38. 38

    Katz SL. The politics of measles. Rep Pediatr Infect Dis 1991;1:1-2

  39. 39

    Wilkins J, Wehrle PF. Additional evidence against measles vaccine administration to infants less than 12 months of age: altered immune response following active/passive immunization. J Pediatr 1979;94:865-869
    CrossRef | Web of Science | Medline

  40. 40

    Ohga S, Okada K, Miyazaki C, Akazawa K, Ueda K. The measles outbreak in Chikuhou District, Fukuoka, Japan, 1990: correlation between herd immunity level and outbreak size. Acta Paediatr Jpn 1992;34:447-453
    Medline

  41. 41

    Cutts FT, Zell ER, Mason D, Bernier RH, Dini EF, Orenstein WA. Monitoring progress toward US preschool immunization goals. JAMA 1992;267:1952-1955
    CrossRef | Web of Science | Medline

  42. 42

    Edmonson MB, Addiss DG, McPherson JT, Berg JL, Circo SR, Davis JP. Mild measles and secondary vaccine failure during a sustained outbreak in a a highly vaccinated population. JAMA 1990;263:2467-2471
    CrossRef | Web of Science | Medline

  43. 43

    Galloway Y, Stehr-Green P. Measles in New Zealand, 1991. Commun Dis N Z 1991;12:107-109

  44. 44

    Carter H, Gorman D. Measles, mumps, and rubella vaccine: time for a two stage policy? BMJ 1992;304:637-637
    CrossRef | Web of Science | Medline

  45. 45

    Lau Y-L, Chow C-B, Leung T-H. Changing epidemiology of measles in Hong Kong from 1961 to 1990 -- impact of a measles vaccination program. J Infect Dis 1992;165:1111-1115
    CrossRef | Web of Science | Medline

  46. 46

    Measles -- United States, 1992. MMWR Morb Mortal Wkly Rep 1993;42:378-381
    Medline

Citing Articles (83)

Citing Articles

  1. 1

    Irene Barrabeig, Ariadna Rovira, Pilar Muñoz, Joan Batalla, Cristina Rius, Josep Anton Sánchez, Àngela Domínguez. (2011) MMR vaccine effectiveness in an outbreak that involved day-care and primary schools. Vaccine 29:45, 8024-8031
    CrossRef

  2. 2

    Young June Choe, Sang Taek Lee, Kyung Min Song, Heeyeon Cho, Geun-Ryang Bae, Jong-Koo Lee. (2010) Surveillance and Control of Rubella in the Republic of Korea From 2001 to 2009: The Necessity for Enhanced Surveillance to Monitor Congenital Rubella Syndrome. Osong Public Health and Research Perspectives 1:1, 23-28
    CrossRef

  3. 3

    Manuela Zlamy, Reinhard Würzner, Heidemarie Holzmann, Anita Brandstätter, Verena Jeller, Lothar Bernd Zimmerhackl, Martina Prelog. (2010) Antibody dynamics after tick-borne encephalitis and measles–mumps–rubella vaccination in children post early thymectomy. Vaccine 28:51, 8053-8060
    CrossRef

  4. 4

    Mohamed Hashem, Mohamed Hasan Husein, Doa’a A. Saleh, Rehab Abdelhai, Eman Eltahlawy, Hala Esmat, Nagah. Horeesh, Mounir Abdalla, Nadia Moustafa, Amany El-Gohary, Nahed Azzazi, Amr Kandeel. (2010) Rubella: Serosusceptibility among Egyptian females in late childhood and childbearing period. Vaccine 28:44, 7202-7206
    CrossRef

  5. 5

    Irja Davidkin, Mia Kontio, Mikko Paunio, Heikki Peltola. (2010) MMR vaccination and disease elimination: the Finnish experience. Expert Review of Vaccines 9:9, 1045-1053
    CrossRef

  6. 6

    Jennifer M. Best, Samantha Cooray, Jangu E. Banatvala. 2010. Rubella. .
    CrossRef

  7. 7

    Stephen C. Hadler, Jane F. Seward. 2010. Immunoprophylaxis of Viral Diseases. .
    CrossRef

  8. 8

    Hugo-Guillermo Ternavasio-de la Vega, Mauro Boronat, Antonio Ojeda, Yaiza García-Delgado, Alfonso Ángel-Moreno, Cristina Carranza-Rodríguez, Raquel Bellini, Adela Francès, Francisco Javier Nóvoa, José-Luis Pérez-Arellano. (2010) Mumps Orchitis in the Post-Vaccine Era (1967-2009). Medicine 89:2, 96-116
    CrossRef

  9. 9

    Pasi Huttunen, Maija Lappalainen, Eeva Salo, Tuula Lönnqvist, Pia Jokela, Timo Hyypiä, Heikki Peltola. (2009) Differential diagnosis of acute central nervous system infections in children using modern microbiological methods. Acta Paediatrica 98:8, 1300-1306
    CrossRef

  10. 10

    Scott A. Halperin, Giuseppe Ferrera, David Scheifele, Gerald Predy, Giuseppe Stella, Mario Cuccia, Martine Douha, Paul Willems. (2009) Safety and immunogenicity of a measles–mumps–rubella–varicella vaccine given as a second dose in children up to six years of age. Vaccine 27:20, 2701-2706
    CrossRef

  11. 11

    Jia-Feng Wu, Yen-Hsuan Ni, Huey-Ling Chen, Hong-Yuan Hsu, Hong-Shiee Lai, Mei-Hwei Chang. (2009) Humoral immunogenicity to measles, rubella, and varicella-zoster vaccines in biliary atresia children. Vaccine 27:21, 2812-2815
    CrossRef

  12. 12

    Inga Velicko, Luise Ledet Müller, Richard Pebody, Bernadette Gergonne, Chinara Aidyralieva, Nina Kostiuchenko, John S. Spika. (2008) Nationwide measles epidemic in Ukraine: The effect of low vaccine effectiveness. Vaccine 26:52, 6980-6985
    CrossRef

  13. 13

    Heikki Peltola, Sari Jokinen, Mikko Paunio, Tapani Hovi, Irja Davidkin. (2008) Measles, mumps, and rubella in Finland: 25 years of a nationwide elimination programme. The Lancet Infectious Diseases 8:12, 796-803
    CrossRef

  14. 14

    G. Gabutti, M. Guido, M.C. Rota, A. De Donno, M.L. Ciofi degli Atti, P. Crovari. (2008) The epidemiology of mumps in Italy. Vaccine 26:23, 2906-2911
    CrossRef

  15. 15

    Kh. MUHSEN, Y. ABOUDY, E. MENDELSON, M. S. GREEN, D. COHEN. (2008) Prevalence of mumps antibodies in the Israeli population in relation to mumps vaccination policy and incidence of disease. Epidemiology and Infection 136:05,
    CrossRef

  16. 16

    Marilyn Baird Mets, Manpreet Singh Chhabra. (2008) Eye Manifestations of Intrauterine Infections and Their Impact on Childhood Blindness. Survey of Ophthalmology 53:2, 95-111
    CrossRef

  17. 17

    Naoko Yoshida, Motoko Fujino, Akiko Miyata, Takao Nagai, Makoto Kamada, Hiroshi Sakiyama, Toshiaki Ihara, Takuji Kumagai, Teruo Okafuji, Takao Okafuji, Tetsuo Nakayama. (2008) Mumps virus reinfection is not a rare event confirmed by reverse transcription loop-mediated isothermal amplification. Journal of Medical Virology 80:3, 517-523
    CrossRef

  18. 18

    Takao Nagai, Teruo Okafuji, Chiaki Miyazaki, Yuhei Ito, Makoto Kamada, Takuji Kumagai, Kenji Yuri, Hiroshi Sakiyama, Akiko Miyata, Toshiaki Ihara, Hitoshi Ochiai, Kunihisa Shimomura, Eitaro Suzuki, Sadayoshi Torigoe, Masahiro Igarashi, Tetsuo Kase, Yoshinobu Okuno, Tetsuo Nakayama. (2007) A comparative study of the incidence of aseptic meningitis in symptomatic natural mumps patients and monovalent mumps vaccine recipients in Japan. Vaccine 25:14, 2742-2747
    CrossRef

  19. 19

    Timo Vesikari, Maija Baer, Paul Willems. (2007) Immunogenicity and Safety of a Second Dose of Measles???Mumps???Rubella???Varicella Vaccine in Healthy Children Aged 5 to 6 Years. The Pediatric Infectious Disease Journal 26:2, 153-158
    CrossRef

  20. 20

    Kyung-Yil Lee, Hyung-Shin Lee, Jae-Kyun Hur, Jin-Han Kang, Byung-Churl Lee. (2007) The changing epidemiology of hospitalized pediatric patients in three measles outbreaks. Journal of Infection 54:2, 167-172
    CrossRef

  21. 21

    S. A. Plotkin. (2006) The History of Rubella and Rubella Vaccination Leading to Elimination. Clinical Infectious Diseases 43:Supplement 3, S164-S168
    CrossRef

  22. 22

    Aysel Celikbas, Onder Ergonul, Sabahat Aksaray, Nilden Tuygun, Harika Esener, Gonul Tanır, Sebnem Eren, Nurcan Baykam, Engin Guvener, Basak Dokuzoguz. (2006) Measles, rubella, mumps, and varicella seroprevalence among health care workers in Turkey: Is prevaccination screening cost-effective?. American Journal of Infection Control 34:9, 583-587
    CrossRef

  23. 23

    Masatoki Kaneko, Hiroshi Sameshima, Tsuyomu Ikenoue, Toshio Minematsu, Kazumi Kusumoto, Satoshi Ibara, Masato Kamitomo, Yuko Maruyama. (2006) Rubella outbreak on Tokunoshima Island in 2004: Serological and epidemiological analysis of pregnant women with rubella. Journal of Obstetrics and Gynaecology Research 32:5, 461-467
    CrossRef

  24. 24

    M. Paunio, H. Peltola, M. Virtanen, P. Leinikki, A. Makela, O. P. Heinonen. (2006) Acute infections, infection pressure, and atopy. Clinical <html_ent glyph="@amp;" ascii="&"/> Experimental Allergy 36:5, 634-639
    CrossRef

  25. 25

    Cornelia Feiterna-Sperling, Rainer Br??nnimann, Annedore Tischer, Peter Stettler, Peter Durrer, Gerhard Gaedicke. (2005) Open Randomized Trial Comparing the Immunogenicity and Safety of a New Measles-Mumps-Rubella Vaccine and a Licensed Vaccine in 12- to 24-Month-Old Children. The Pediatric Infectious Disease Journal 24:12, 1083-1088
    CrossRef

  26. 26

    Richard Harling, Joanne M. White, Mary E. Ramsay, Karen F. Macsween, Corry van den Bosch. (2005) The effectiveness of the mumps component of the MMR vaccine: a case control study. Vaccine 23:31, 4070-4074
    CrossRef

  27. 27

    Wieslawa Janaszek-Seydlitz, Bozena Bucholc, Paulina Gorska, Janusz Slusarczyk. (2005) Mumps in Poland since 1990 to 2003; epidemiology and antibody prevalence. Vaccine 23:21, 2711-2716
    CrossRef

  28. 28

    E. Delaporte, C.-A. Wyler-Lazarevic, J.-L. Richard, P. Sudre. (2004) Contribution des fratries non vaccinées à une flambée de rougeole en Suisse. Revue d'Épidémiologie et de Santé Publique 52:6, 493-501
    CrossRef

  29. 29

    Amra Uzicanin, Fangjun Zhou, Rudi Eggers, Elize Webb, Peter Strebel. (2004) Economic analysis of the 1996–1997 mass measles immunization campaigns in South Africa. Vaccine 22:25-26, 3419-3426
    CrossRef

  30. 30

    Corinne Vandermeulen, Mathieu Roelants, Marijke Vermoere, Katelijn Roseeuw, Patrick Goubau, Karel Hoppenbrouwers. (2004) Outbreak of mumps in a vaccinated child population: a question of vaccine failure?. Vaccine 22:21-22, 2713-2716
    CrossRef

  31. 31

    Helen Petousis-Harris, Felicity Goodyear-Smith, Nikki Turner, Ben Soe. (2004) Family physician perspectives on barriers to childhood immunisation. Vaccine 22:17-18, 2340-2344
    CrossRef

  32. 32

    Peter M. Strebel, Ana‐Maria Henao‐Restrepo, Edward Hoekstra, Jean‐Marc Olivé, Mark J. Papania, Stephen L. Cochi. (2004) Global Measles Elimination Efforts: The Significance of Measles Elimination in the United States. The Journal of Infectious Diseases 189:s1, S251-S257
    CrossRef

  33. 33

    Judith Petts, Simon Niemeyer. (2004) Health risk communication and amplification: learning from the MMR vaccination controversy. Health, Risk & Society 6:1, 7-23
    CrossRef

  34. 34

    Mikko Paunio, Klaus Hedman, Irja Davidkin, Heikki Peltola. (2003) IgG avidity to distinguish secondary from primary measles vaccination failures: prospects for a more effective global measles elimination strategy. Expert Opinion on Pharmacotherapy 4:8, 1215-1225
    CrossRef

  35. 35

    Bracha Rager-Zisman, Elina Bazarsky, Agneta Skibin, Shlomo Chamney, Ilana Belmaker, Iris Shai, Ella Kordysh, Diane E Griffin. (2003) The effect of measles–mumps–rubella (MMR) immunization on the immune responses of previously immunized primary school children. Vaccine 21:19-20, 2580-2588
    CrossRef

  36. 36

    Dalya Güriş, Yıldırım Bayazıt, Ümit Özdemirer, Vedat Buyurgan, Cevdet Yalnız, İsmail Toprak, Sefer Aycan. (2003) Measles Epidemiology and Elimination Strategies in Turkey. The Journal of Infectious Diseases 187:s1, S230-S234
    CrossRef

  37. 37

    Trevor Duke, Charles S Mgone. (2003) Measles: not just another viral exanthem. The Lancet 361:9359, 763-773
    CrossRef

  38. 38

    May-Lill Garly, Peter Aaby. (2003) The challenge of improving the efficacy of measles vaccine. Acta Tropica 85:1, 1-17
    CrossRef

  39. 39

    Marjaleena Koskiniemi, Heli Piiparinen, Timo Rantalaiho, Pekka Eränkö, Markus Färkkilä, Kirsti Räihä, Eeva-Marjatta Salonen, Pentti Ukkonen, Antti Vaheri. (2002) Acute central nervous system complications in varicella zoster virus infections. Journal of Clinical Virology 25:3, 293-301
    CrossRef

  40. 40

    Chin-Yun Lee, Ren-Bin Tang, Fu-Yuan Huang, Haiwen Tang, Li-Min Huang, Hans L. Bock. (2002) A new measles mumps rubella (MMR) vaccine: a randomized comparative trial for assessing the reactogenicity and immunogenicity of three consecutive production lots and comparison with a widely used MMR vaccine in measles primed children. International Journal of Infectious Diseases 6:3, 202-209
    CrossRef

  41. 41

    Michael Rothberg, Michael L. Bennish, Jack S. Kao, John B. Wong. (2002) Do the Benefits of Varicella Vaccination Outweigh the Long‐Term Risks? A Decision‐Analytic Model for Policymakers and Pediatricians. Clinical Infectious Diseases 34:7, 885-894
    CrossRef

  42. 42

    (2002) Immunology Series: Vaccines. New England Journal of Medicine 346:11, 864-866
    Full Text

  43. 43

    David A.C. Elliman, Helen E. Bedford. (2002) Measles, Mumps and Rubella Vaccine, Autism and Inflammatory Bowel Disease. Pediatric Drugs 4:10, 631-635
    CrossRef

  44. 44

    R.G Pebody, N.J Gay, L.M Hesketh, A Vyse, P Morgan-Capner, D.W Brown, P Litton, E Miller. (2002) Immunogenicity of second dose measles–mumps–rubella (MMR) vaccine and implications for serosurveillance. Vaccine 20:7-8, 1134-1140
    CrossRef

  45. 45

    Maurice R Hilleman. (2001) Current overview of the pathogenesis and prophylaxis of measles with focus on practical implications. Vaccine 20:5-6, 651-665
    CrossRef

  46. 46

    Stanley A Plotkin. (2001) Rubella eradication. Vaccine 19:25-26, 3311-3319
    CrossRef

  47. 47

    Timo Rantalaiho, Markus Färkkilä, Antti Vaheri, Marjaleena Koskiniemi. (2001) Acute encephalitis from 1967 to 1991. Journal of the Neurological Sciences 184:2, 169-177
    CrossRef

  48. 48

    ANNAMARI PATJA, IRJA DAVIDKIN, TAPIO KURKI, MARKKU J. T. KALLIO, MARTTI VALLE, HEIKKI PELTOLA. (2000) Serious adverse events after measles-mumps-rubella vaccination during a fourteen-year prospective follow-up. The Pediatric Infectious Disease Journal 19:12, 1127-1134
    CrossRef

  49. 49

    W. A. Orenstein, P. M. Strebel, M. Papania, R. W. Sutter, W. J. Bellini, S. L. Cochi. (2000) Measles eradication: is it in our future?. American Journal of Public Health 90:10, 1521-1525
    CrossRef

  50. 50

    Irja Davidkin, Heikki Peltola, Pauli Leinikki, Martti Valle. (2000) Duration of rubella immunity induced by two-dose measles, mumps and rubella (MMR) vaccination. A 15-year follow-up in Finland. Vaccine 18:27, 3106-3112
    CrossRef

  51. 51

    P. Crovari, G. Gabutti, G. Giammanco, P. Dentico, A.R. Moiraghi, F. Ponzio, R. Soncini. (2000) Reactogenicity and immunogenicity of a new combined Measles–Mumps–Rubella vaccine: results of a multicentre trial. Vaccine 18:25, 2796-2803
    CrossRef

  52. 52

    Athmanundh Dilraj, Felicity T Cutts, J Fernandez de Castro, Jeremy G Wheeler, David Brown, Cathy Roth, Hoosen M Coovadia, John V Bennett. (2000) Response to different measles vaccine strains given by aerosol and subcutaneous routes to schoolchildren: a randomised trial. The Lancet 355:9206, 798-803
    CrossRef

  53. 53

    S Aksit, A Egemen, T Ozacar, Z Kurugol. (2000) Mumps seroprevalence in an unvaccinated population in Izmir, Turkey. Acta Paediatrica 89:3, 370-371
    CrossRef

  54. 54

    A Tischer, E Gerike. (2000) Immune response after primary and re-vaccination with different combined vaccines against measles, mumps, rubella. Vaccine 18:14, 1382-1392
    CrossRef

  55. 55

    Lyndal Bond, Terry Nolan, Rosemary Lester. (1999) Immunisation uptake, services required and government incentives for users of formal day care. Australian and New Zealand Journal of Public Health 23:4, 368-376
    CrossRef

  56. 56

    SADIK AKSIT, AYTEN EGEMEN, TIJEN OZACAR, ZAFER KURUGOL, PEMBE KESKINOGLU, MELTEM TASBAKAN, SUAT CAGLAYAN. (1999) Rubella seroprevalence in an unvaccinated population in İzmir: recommendations for rubella vaccination in Turkey. The Pediatric Infectious Disease Journal 18:7, 577-580
    CrossRef

  57. 57

    M. Khalil, A.A. Poltera, M. Al-Howasi, C. Herzog, E. Gerike, B. Wegmüller, R. Glück. (1999) Response to measles revaccination among toddlers in Saudi Arabia by the use of two different trivalent measles-mumps-rubella vaccines. Transactions of the Royal Society of Tropical Medicine and Hygiene 93:2, 214-219
    CrossRef

  58. 58

    A Domı́nguez, J Vidal, P Plans, G Carmona, P Godoy, J Batalla, L Salleras. (1999) Measles immunity and vaccination policy in Catalonia. Vaccine 17:6, 530-534
    CrossRef

  59. 59

    VYTAUTAS USONIS, VYTAUTAS BAKASENAS, ACHIM KAUFHOLD, KERIM CHITOUR, RALF CLEMENS. (1999) Reactogenicity and immunogenicity of a new live attenuated combined measles, mumps and rubella vaccine in healthy children. The Pediatric Infectious Disease Journal 18:1, 42-48
    CrossRef

  60. 60

    Mark A. Miller, Stephen Redd, Stephen Hadler, Alan Hinman. (1998) A model to estimate the potential economic benefits of measles eradication for the United States. Vaccine 16:20, 1917-1922
    CrossRef

  61. 61

    Irja Davidkin, Martti Valle. (1998) Vaccine-induced measles virus antibodies after two doses of combined measles, mumps and rubella vaccine: a 12-year follow-up in two cohorts. Vaccine 16:20, 2052-2057
    CrossRef

  62. 62

    LEENA REHNBERG-LAIHO, HILPI RAUTELIN, MARTTI VALLE, TIMO U. KOSUNEN. (1998) Persisting Helicobacter antibodies in Finnish children and adolescents between two and twenty years of age. The Pediatric Infectious Disease Journal 17:9, 796-799
    CrossRef

  63. 63

    Daniel Germann, Meri Gorgievski, Angelika Ströhle, Lukas Matter. (1998) Detection of mumps virus in clinical specimens by rapid centrifugation culture and conventional tube cell culture. Journal of Virological Methods 73:1, 59-64
    CrossRef

  64. 64

    V. Usonis, V. Bakasenas, K. Chitour, R. Clemens. (1998) Comparative study of reactogenicity and immunogenicity of new and established measles, mumps and rubella vaccines in healthy children. Infection 26:4, 222-226
    CrossRef

  65. 65

    Elina M. Mäki-Torkko, Päivi K. Lindholm, Mirja R.H. Väyrynen, Jaakko T. Leisti, Martti J. Sorri. (1998) Epidemiology of Moderate to Profound Childhood Hearing Impairments in Northern Finland. Any Changes in Ten Years?. Scandinavian Audiology 27:2, 95-103
    CrossRef

  66. 66

    Kristina Broliden, Elba Rubilar Abreu, Malin Arneborn, Margareta Böttiger. (1998) Immunity to mumps before and after MMR vaccination at 12 years of age in the first generation offered the two-dose immunization programme. Vaccine 16:2-3, 323-327
    CrossRef

  67. 67

    Simone Schwarzer, Susanne Reibel, Alois B. Lang, Mark Michael Struck, Beatriz Finkel, Edith Gerike, Annedore Tischer, Markus Gassner, Reinhard Glück, Burghard Stück, Stanley J. Cryz. (1998) Safety and characterization of the immune response engendered by two combined measles, mumps and rubella vaccines. Vaccine 16:2-3, 298-304
    CrossRef

  68. 68

    KARI LUOTOLA, HEIKKI HYÖTY, JORMA SALMI, ARI MIETTINEN, HEIKKI HELIN, AMOS PASTERNACK. (1998) Evaluation of infectious etiology in subacute thyroiditis - lack of association with coxsackievirus infection. APMIS 106:1-6, 500-504
    CrossRef

  69. 69

    Olli P Heinonen, Mikko Paunio, Heikki Peltola. (1998) Total elimination of measles in Finland. Annals of Medicine 30:2, 131-133
    CrossRef

  70. 70

    Roberto Casella, Bernhard Leibundgut, Kurt Lehmann, Thomas C. Gasser. (1997) MUMPS ORCHITIS: REPORT OF A MINI-EPIDEMIC. The Journal of Urology 158:6, 2158-2161
    CrossRef

  71. 71

    Heikki Peltola, Irja Davidkin, Martti Valle, Mikko Paunio, Tapani Hovi, Olli P Heinonen, Pauli Leinikki. (1997) No measles in Finland. The Lancet 350:9088, 1364-1365
    CrossRef

  72. 72

    J.J. Chomel, Y. Robin, R. Durdilly, D. Thouvenot, M. Langlois, M. Aymard. (1997) Rapid direct diagnosis of mumps meningitis by ELISA capture technique. Journal of Virological Methods 68:1, 97-104
    CrossRef

  73. 73

    Margareta Böttiger, Marianne Forsgren. (1997) Twenty years' experience of rubella vaccination in Sweden: 10 years of selective vaccination (of 12-year-old girls and of women postpartum) and 13 years of a general two-dose vaccination. Vaccine 15:14, 1538-1544
    CrossRef

  74. 74

    KEIKO ODA, HIROHISA KATO, AKIO KONISHI. (1996) The outbreak of mumps in a small island in Japan. Pediatrics International 38:3, 224-228
    CrossRef

  75. 75

    Pentti Ukkonen. (1996) Rubella Immunity and Morbidity: Impact of Different Vaccination Programs in Finland 1979–1992. Scandinavian Journal of Infectious Diseases 28:1, 31-35
    CrossRef

  76. 76

    Daniel Germann, Angelika Ströhle, Kurt Eggenberger, Charles-André Steiner, Lukas Matter. (1996) An Outbreak of Mumps in a Population Partially Vaccinated with the Rubini Strain. Scandinavian Journal of Infectious Diseases 28:3, 235-238
    CrossRef

  77. 77

    B. G. Williams, F. T. Cutts, C. Dye. (1995) Measles vaccination policy. Epidemiology and Infection 115:03, 603
    CrossRef

  78. 78

    A. Ndikuyeze, A. Cook, F. T. Cutts, S. Bennett. (1995) Priorities in global measles control: report of an outbreak in N'Djamena, Chad. Epidemiology and Infection 115:02, 309
    CrossRef

  79. 79

    (1995) The Measles–Mumps–Rubella Vaccination Program in Finland. New England Journal of Medicine 332:16, 1102-1103
    Full Text

  80. 80

    Angelika Strhle, Daniel Germann. (1995) Mumpsimpfstoffe: Virologische Grundlagen. Sozial- und Prventivmedizin SPM 40:2, 102-109
    CrossRef

  81. 81

    Wolfram J.P. Karges, Jorma Ilonen, Brian H. Robinson, Hans-Michael Dosch. (1995) Self and non-self antigen in diabetic autoimmunity: Molecules and mechanisms. Molecular Aspects of Medicine 16:2, 79-213
    CrossRef

  82. 82

    Irja Davidkin, Martti Valle, Ilkka Julkunen. (1995) Persistence of anti-mumps virus antibodies after a two-dose MMR vaccination. A nine-year follow-up. Vaccine 13:16, 1617-1622
    CrossRef

  83. 83

    Heisler, Michael B., , Richmond, Julius B., . (1994) Lessons from Finland's Successful Immunization Program. New England Journal of Medicine 331:21, 1446-1447
    Full Text

Letters