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William A. Gahl

Section on Human Biochemical Genetics

National Institute of Child Health and Human Development

National Institutes of Health

MSC 1851 Building 10

USA

[email]@helix.nih.gov

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Affiliations

Section on Human Biochemical Genetics, National Institute of Child Health and Human Development, National Institutes of Health, MSC 1851 Building 10, USA. 2003 - 2008
National Human Genome Research Institute and Intramural Office of Rare Diseases, National Institutes of Health, Bethesda, Maryland 20892-1851, USA. 2007
Heritable Disorders Branch, National Institute of Child Health and Human Development, Bethesda, Md 20892-1830, USA. 2002

References

Chemical individuality: concept and outlook. Gahl, W.A. J. Inherit. Metab. Dis. (2008) [Pubmed]
Nephropathic cystinosis in adults: natural history and effects of oral cysteamine therapy. Gahl, W.A., Balog, J.Z., Kleta, R. Ann. Intern. Med. (2007) [Pubmed]
Engulfed. Gahl, W.A. Mol. Genet. Metab. (2006) [Pubmed]
Early oral cysteamine therapy for nephropathic cystinosis. Gahl, W.A. Eur. J. Pediatr. (2003) [Pubmed]
Cystinosis. Gahl, W.A., Thoene, J.G., Schneider, J.A. N. Engl. J. Med. (2002) [Pubmed]
Effect of pirfenidone on the pulmonary fibrosis of Hermansky-Pudlak syndrome. Gahl, W.A., Brantly, M., Troendle, J., Avila, N.A., Padua, A., Montalvo, C., Cardona, H., Calis, K.A., Gochuico, B. Mol. Genet. Metab. (2002) [Pubmed]