Melissa A Parisi

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc Clinical and molecular features of Joubert syndrome and related disorders
    Melissa A Parisi
    Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Boulevard, Bethesda, MD 20892 7510, USA
    Am J Med Genet C Semin Med Genet 151:326-40. 2009
  2. pmc We don't know what we don't study: the case for research on medication effects in pregnancy
    Melissa A Parisi
    Intellectual and Developmental Disabilities Branch, Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Boulevard, Bethesda, MD 20892 7510, USA
    Am J Med Genet C Semin Med Genet 157:247-50. 2011
  3. pmc MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome
    Meral Gunay-Aygun
    Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA
    J Pediatr 155:386-92.e1. 2009

Detail Information

Publications3

  1. pmc Clinical and molecular features of Joubert syndrome and related disorders
    Melissa A Parisi
    Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Boulevard, Bethesda, MD 20892 7510, USA
    Am J Med Genet C Semin Med Genet 151:326-40. 2009
    ....
  2. pmc We don't know what we don't study: the case for research on medication effects in pregnancy
    Melissa A Parisi
    Intellectual and Developmental Disabilities Branch, Center for Developmental Biology and Perinatal Medicine, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Boulevard, Bethesda, MD 20892 7510, USA
    Am J Med Genet C Semin Med Genet 157:247-50. 2011
    ..Although this is a start, there is a critical need for further research on medications used during pregnancy, especially their effects on both the mother and her developing child...
  3. pmc MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome
    Meral Gunay-Aygun
    Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA
    J Pediatr 155:386-92.e1. 2009
    ..To describe 3 children with mutations in a Meckel syndrome gene (MKS3), with features of autosomal recessive polycystic kidney disease (ARPKD), nephronophthisis, and Joubert syndrome (JS)...