Clinical and laboratory findings and etiologies of genetic homocystinemia: a single-center experience.

Besen, Seyda; Ozkale, Yasemin; Ceylaner, Serdar; Noyan, Aytul; Erol, Ilknur

Besen, Seyda; Ozkale, Yasemin; Ceylaner, Serdar; Noyan, Aytul; Erol, Ilknur.

Afiliação

Besen S; Division of Neurology, Faculty of Medicine, Adana Dr. Turgut Noyan Teaching and Medical Research Center, Baskent University, Adana, Turkey.
Ozkale Y; Division of Pediatrics, Faculty of Medicine, Adana Teaching and Medical Research Center, Baskent University, BarajYolu 1 Durak, Seyhan, 01120, Adana, Turkey. dryaseminozkale@gmail.com.
Ceylaner S; Clinical Genetics Unit, Intergen Genetics and Rare Diseases Research and Application Center, Ankara, Turkey.
Noyan A; Division of Nephrology, Faculty of Medicine, Adana Dr. Turgut Noyan Teaching and Medical Research Center, Baskent University, Adana, Turkey.
Erol I; Division of Neurology, Faculty of Medicine, Adana Dr. Turgut Noyan Teaching and Medical Research Center, Baskent University, Adana, Turkey.

Acta Neurol Belg ; 124(1): 213-222, 2024 Feb.

Article em En | MEDLINE | ID: mdl-37728847

Assuntos

Hiper-Homocisteinemia; Acidente Vascular Cerebral; Criança; Humanos; Adolescente; Hiper-Homocisteinemia/genética; Hiper-Homocisteinemia/metabolismo; Estudos Retrospectivos; Aminoácidos

Palavras-chave

Children; Hyperhomocysteinemia; Neurologic symptoms

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hiper-Homocisteinemia / Acidente Vascular Cerebral Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adolescent / Child / Humans Idioma: En Revista: Acta Neurol Belg Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Turquia

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