Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction
- 1 January 1990
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 116 (1), 88-94
- https://doi.org/10.1016/s0022-3476(05)81651-8
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Biochemical abnormalities in rhizomelic chondrodysplasia punctataThe Journal of Pediatrics, 1988
- Peroxisomal Enzyme Deficiency in the Conradi–Hunerman Form of Chondrodysplasia PunctataNew England Journal of Medicine, 1987
- The Cerebrohepatorenal (Zellweger) Syndrome: An Improved Method for the Biochemical Diagnosis and its Potential Value for Prenatal DetectionPediatric Research, 1985
- Postpartum Rubella Immunization: Association with Development of Prolonged Arthritis, Neurological Sequelae, and Chronic Rubella ViremiaThe Journal of Infectious Diseases, 1985
- Delayed Manifestations of Congenital RubellaClinical Infectious Diseases, 1985
- PERSISTENT RUBELLA INFECTION AND RUBELLA-ASSOCIATED ARTHRITISThe Lancet, 1982
- AdrenoleukodystrophyNeurology, 1981
- Loss of Rubella Hemagglutination Inhibition Antibody in Congenital RubellaAmerican Journal of Diseases of Children, 1971
- Congenital rubella syndrome as a systemic infection. Studies of affected infants born in Philadelphia, U.S.A.BMJ, 1965
- Arthrogryposis Multiplex CongenitaArchives of Neurology, 1961