Epilepsy in Biotinidase Deficiency After Biotin Treatment-Reference-Cited by-同舟云学术

Epilepsy in Biotinidase Deficiency After Biotin Treatment

Published:2011 Issue: Volume: Page:75-78
ISSN:2192-8304
Container-title:JIMD Reports
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Author:

Micó Salvador Ibáñez,Jiménez Rosario Domingo,Salcedo Eduardo Martínez,Martínez Helena Alarcón,Mira Alberto Puche,Fernández Carlos Casas

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/8904_2011_74

Reference15 articles.

1. Baumgartner ER, Suormala T (1997) Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism. Int J Vitam Nutr Res 67(5):377–384

2. Bunch M, Singh A (2011) Peculiar neuroimaging and electrophysiological findings in a patient with biotinidase deficiency. Seizure 20(1):83–86

3. Couce Pico ML, Martinón-Torres F, Castiñeiras DE et al (1999) Biotinidase deficiency: importance of its neonatal diagnosis and early treatment. An Esp Pediatr 50:504–506

4. Desai S, Ganesan K, Hegde A (2008) Biotinidase deficiency: a reversible metabolic encephalopathy. Neuroimaging and MR spectroscopic findings in a series of four patients. Pediatr Radiol 38(8):848–856

5. Lafuente-Hidalgo M, Ranz Angulo R, López Pisón J et al (2010) Epileptic encephalopathy due to partial biotinidase deficiency. An Pediatr (Barc) 72(3):227–228

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