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The Utility of CSF for the Diagnosis of Primary and Secondary Monoamine Neurotransmitter Deficiencies.
Burlina, A B; Celato, A; Polo, G; Edini, C; Burlina, A P.
Afiliação
  • Burlina AB; Division of Inherited Metabolic Diseases, Reference Centre Expanded Newborn Screening, Department of Women's and Children's Health, University Hospital, Padova, Italy.
  • Celato A; Division of Inherited Metabolic Diseases, Reference Centre Expanded Newborn Screening, Department of Women's and Children's Health, University Hospital, Padova, Italy.
  • Polo G; Division of Inherited Metabolic Diseases, Reference Centre Expanded Newborn Screening, Department of Women's and Children's Health, University Hospital, Padova, Italy.
  • Edini C; Division of Inherited Metabolic Diseases, Reference Centre Expanded Newborn Screening, Department of Women's and Children's Health, University Hospital, Padova, Italy.
  • Burlina AP; Neurological Unit, St. Bassiano Hospital, Bassano del Grappa, Italy.
EJIFCC ; 28(1): 64-76, 2017 Mar.
Article em En | MEDLINE | ID: mdl-28439219
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article