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Expert Review of Neurotherapeutics Volume 16, 2016 - Issue 7
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Review

Treatment of genetic defects of thiamine transport and metabolism

Juan Darío Ortigoza-EscobarDepartment of Child Neurology, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain;Department of Child Neurology, Hospital General de Granollers, Barcelona, Spain
,
Marta Molero-LuisClinical Biochemistry, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain;Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain
,
Angela AriasDivision of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics, Hospital Clinic, Barcelona, Spain;Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain
,
Laura Martí-SánchezDepartment of Child Neurology, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain;Clinical Biochemistry, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain
,
Pilar Rodriguez-PomboDepartamento de Biología Molecular, Centro de Diagnóstico de Enfermedades Moleculares (CEDEM), Centro de Biología Molecular Severo Ochoa CSIC-UAM, IDIPAZ, Universidad Autónoma de Madrid, Madrid, Spain;Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain
,
Rafael ArtuchClinical Biochemistry, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain;Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain
&
Belén Pérez-DueñasDepartment of Child Neurology, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain;Centre for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, SpainCorrespondence[email protected]
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Pages 755-763 | Received 11 Feb 2016, Accepted 05 May 2016, Published online: 23 May 2016

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