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Molecular and Cellular Probes|November 8, 2005
Single nucleotide polymorphisms in the apoptosis receptor gene TNFRSF6Julie E Niemela, Amy P Hsu, Thomas A Fleisher, et al.The Journal of Allergy and Clinical Immunology|March 9, 2017
Treatment of infants identified as having severe combined immunodeficiency by means of newborn screeningMorna J Dorsey, Christopher C Dvorak, Morton J Cowan, et al.Nature Reviews. Disease Primers|May 19, 2016
Severe combined immunodeficiencies and related disordersAlain Fischer, Luigi D Notarangelo, Bénédicte Neven, et al.Hematology. American Society of Hematology. Education Program|November 25, 2003
Immunodeficiency disordersMax D Cooper, Lewis L Lanier, Mary Ellen Conley, et al.Blood|January 25, 2002
Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survivalLaurie A Myers, Dhavalkumar D Patel, Jennifer M Puck, et al.Clinical Immunology (Orlando, Fla.)|February 14, 2004
Abnormal development of thymic dendritic and epithelial cells in human X-linked severe combined immunodeficiencyLaura P Hale, Rebecca H Buckley, Jennifer M Puck, et al.Pediatrics|January 6, 2016
Parental Views on Expanded Newborn Screening Using Whole-Genome SequencingGalen Joseph, Flavia Chen, Julie Harris-Wai, et al.Molecular Genetics and Metabolism|August 4, 2011
A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID)Kee Chan, Joie Davis, Sung-Yun Pai, et al.Archives of Dermatology|September 24, 2004
Dermatitis and the newborn rash of hyper-IgE syndromeCheryl Lee D Eberting, Joie Davis, Jennifer M Puck, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarrayTonya Lebet, Richard Chiles, Amy P Hsu, et al.Pageof 16