Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome.

Akasaka, Manami; Kamei, Atsushi; Araya, Nami; Oyama, Kotaro; Sasaki, Makoto

Akasaka, Manami; Kamei, Atsushi; Araya, Nami; Oyama, Kotaro; Sasaki, Makoto.

Afiliação

Akasaka M; Department of Pediatrics, School of Medicine, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.
Kamei A; Department of Pediatrics, School of Medicine, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.
Araya N; Department of Pediatrics, School of Medicine, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.
Oyama K; Department of Pediatrics, School of Medicine, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.
Sasaki M; Division of Ultrahigh Field MRI, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.

Pediatr Int ; 60(10): 978-979, 2018 Oct.

Article em En | MEDLINE | ID: mdl-30320424

Assuntos

Erros Inatos do Metabolismo dos Carboidratos/diagnóstico por imagem; Proteínas de Transporte de Monossacarídeos/deficiência; Espectroscopia de Prótons por Ressonância Magnética/métodos; Pré-Escolar; Transportador de Glucose Tipo 1/genética; Humanos; Lactente; Recém-Nascido

Palavras-chave

glucose transporter type 1 deficiency syndrome; glutamate-glutamine complex; hypoglycorrhachia; proton magnetic resonance spectroscopy; thalamus

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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