Perplexing Etiology of Hyperphenylalaninemia in an Infant Referred via Newborn Screening.

Çiki, Kismet; Akar, H Tuna; Özgül, R Köksal; Gülbakan, Basri; Yildiz, Yilmaz

Çiki, Kismet; Akar, H Tuna; Özgül, R Köksal; Gülbakan, Basri; Yildiz, Yilmaz.

Afiliación

Çiki K; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Akar HT; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Özgül RK; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Ankara, Turkey.
Gülbakan B; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Ankara, Turkey.
Yildiz Y; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Clin Chem ; 67(10): 1428-1431, 2021 10 01.

Article en En | MEDLINE | ID: mdl-34597372

Asunto(s)

Tamizaje Neonatal; Fenilcetonurias; Humanos; Lactante; Recién Nacido; Tamizaje Masivo; Fenilcetonurias/diagnóstico

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenilcetonurias / Tamizaje Neonatal Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Screening_studies Límite: Humans / Infant / Newborn Idioma: En Revista: Clin Chem Asunto de la revista: QUIMICA CLINICA Año: 2021 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Reino Unido

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