Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors

Author:

Ortigoza-Escobar Juan Darío12,Alfadhel Majid3,Molero-Luis Marta4,Darin Niklas5,Spiegel Ronen6,de Coo Irenaeus F.7,Gerards Mike8,Taylor Robert W.9,Artuch Rafael2410,Nashabat Marwan3,Rodríguez-Pombo Pilar1011,Tabarki Brahim12,Pérez-Dueñas Belén1210,

Affiliation:

1. Division of Child Neurology, Sant Joan de Déu Hospital; University of Barcelona; Barcelona Spain

2. Institut de Recerca Sant Joan de Déu; University of Barcelona; Barcelona Spain

3. Division of Genetics, Department of Pediatrics; King Saud bin Abdulaziz University for Health Sciences; Riyadh Saudi Arabia

4. Division of Biochemistry, Sant Joan de Déu Hospital; University of Barcelona; Barcelona Spain

5. Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy; University of Gothenburg; Gothenburg Sweden

6. Rappaport School of Medicine, Technion, Haifa, Israel; Department of Pediatrics B; Emek Medical Center; Afula Israel

7. Department of Neurology; Erasmus MC-Sophia Children's Hospital; Rotterdam The Netherlands

8. MaCSBio (Maastricht Centre for Systems Biology); Maastricht University Medical Centre; Maastricht The Netherlands

9. Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience; Newcastle University; Newcastle upon Tyne United Kingdom

10. CIBERER; Instituto de Salud Carlos III; Barcelona Spain

11. Departamento 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

12. Divisions of Pediatric Neurology; Prince Sultan Military Medical City; Riyadh Saudi Arabia

Funder

“Plan Nacional de I+D+I and Instituto de Salud Carlos III-Subdirección General de Evaluación y Fomento de la Investigación Sanitaria”

Rio Hortega

European Social Fund

Wellcome Centre for Mitochondrial Research

Medical Research Council (MRC) Centre for Translational Research in Neuromuscular Disease, Mitochondrial Disease Patient Cohort (UK)

Lily Foundation

UK NHS Highly Specialized Service for Rare Mitochondrial Disorders of Adults and Children

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference65 articles.

1. Thiamine in Clinical Practice;Frank;JPEN J Parenter Enteral Nutr,2015

2. Defects of thiamine transport and metabolism;Brown;J Inherit Metab Dis,2014

3. Putamina involvement in Wernicke encephalopathy induced by Janus Kinase 2 inhibitor;Rodríguez-Pardo;Clin Neuropharmacol,2015

4. Beriberi (thiamine deficiency) and high infant mortality in northern Laos;Barennes;PLoS Negl Trop Dis,2015

5. Perinatal consumption of thiamine-fortified fish sauce in rural Cambodia: a randomized clinical trial;Whitfield;JAMA Pediatr,2016

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