Development of population-based newborn screening for severe combined immunodeficiency
Top Cited Papers
Open Access
- 1 February 2005
- journal article
- Published by Elsevier in Journal of Allergy and Clinical Immunology
- Vol. 115 (2) , 391-398
- https://doi.org/10.1016/j.jaci.2004.10.012
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Janus kinase 3 (JAK3) deficiency: clinical, immunologic, and molecular analyses of 10 patients and outcomes of stem cell transplantationBlood, 2004
- The future of gene therapyNature, 2004
- Mutations in genes required for T-cell development:IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE reviewGenetics in Medicine, 2004
- Reticular dysgenesis: HLA non-identical bone marrow transplants in a series of 10 patientsBone Marrow Transplantation, 2002
- Genetic Screening of NewbornsAnnual Review of Genomics and Human Genetics, 2000
- Thymic Function after Hematopoietic Stem-Cell Transplantation for the Treatment of Severe Combined ImmunodeficiencyNew England Journal of Medicine, 2000
- Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infantsThe Journal of Pediatrics, 1997
- PEG-ADA replacement therapy for adenosine deaminase deficiency: an update after 8.5 yearsClinical Immunology and Immunopathology, 1995
- Application of Molecular Genetics in Public Health: Improved Follow-up in a Neonatal Hemoglobinopathy Screening ProgramBiochemical Medicine and Metabolic Biology, 1994
- Prospective Study of Early Neonatal Screening for PhenylketonuriaNew England Journal of Medicine, 1981