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Neurologic and neurodevelopmental phenotypes in young children with early-treated combined methylmalonic acidemia and homocystinuria, cobalamin C type.
Weisfeld-Adams, James D; Bender, H Allison; Miley-Åkerstedt, Anna; Frempong, Tamiesha; Schrager, Nina L; Patel, Keyur; Naidich, Thomas P; Stein, Victoria; Spat, Jessica; Towns, Stephanie; Wasserstein, Melissa P; Peter, Inga; Frank, Yitzchak; Diaz, George A.
Afiliação
  • Weisfeld-Adams JD; Departments of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: james.weisfeld-adams@mssm.edu.
Mol Genet Metab ; 110(3): 241-7, 2013 Nov.
Article em En | MEDLINE | ID: mdl-23954310
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Erros Inatos do Metabolismo dos Aminoácidos / Homocistinúria Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2013 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Erros Inatos do Metabolismo dos Aminoácidos / Homocistinúria Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2013 Tipo de documento: Article