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Treatment of genetic defects of thiamine transport and metabolism.
Ortigoza-Escobar, Juan Darío; Molero-Luis, Marta; Arias, Angela; Martí-Sánchez, Laura; Rodriguez-Pombo, Pilar; Artuch, Rafael; Pérez-Dueñas, Belén.
Affiliation
  • Ortigoza-Escobar JD; a Department of Child Neurology, Hospital Sant Joan de Déu , University of Barcelona , Barcelona , Spain.
  • Molero-Luis M; f Department of Child Neurology , Hospital General de Granollers , Barcelona , Spain.
  • Arias A; b Clinical Biochemistry, Hospital Sant Joan de Déu , University of Barcelona , Barcelona , Spain.
  • Martí-Sánchez L; e Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII , Madrid , Spain.
  • Rodriguez-Pombo P; c Division of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics , Hospital Clinic , Barcelona , Spain.
  • Artuch R; e Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII , Madrid , Spain.
  • Pérez-Dueñas B; a Department of Child Neurology, Hospital Sant Joan de Déu , University of Barcelona , Barcelona , Spain.
Expert Rev Neurother ; 16(7): 755-63, 2016 07.
Article in En | MEDLINE | ID: mdl-27191787
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Transport Proteins / Anemia, Megaloblastic Type of study: Screening_studies Limits: Humans Language: En Journal: Expert Rev Neurother Journal subject: NEUROLOGIA / TERAPEUTICA Year: 2016 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Transport Proteins / Anemia, Megaloblastic Type of study: Screening_studies Limits: Humans Language: En Journal: Expert Rev Neurother Journal subject: NEUROLOGIA / TERAPEUTICA Year: 2016 Document type: Article Affiliation country: