Multiple Carboxylase Deficiency-Reference-Cited by-同舟云学术

Multiple Carboxylase Deficiency

Published:2005 Issue: Volume: Page:248-251
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Container-title:Magnetic Resonance of Myelination and Myelin Disorders
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Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/3-540-27660-2_30

Reference42 articles.

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2. Baumgartner ER, Suormala TM, Wick H, Probst A, Blauenstein U, Bachmann C, Vest M. Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome. Pediatr Res 1989; 26: 260–266

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

4. Bay CA, Berry GT, Glauser TA, Hayward JC, Wolf B, Sladky JT, Kaplan P. Reversible metabolic myopathy in biotinidase deficiency: its possible role in causing hypotonia. J Inherit Metab Dis 1995; 18: 701–704

5. Bousounis DP, Camfield PR, Wolf B. Reversal of brain atrophy with biotin treatment in biotinidase deficiency. Neuropediatrics 1993; 24: 214–217

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2. Brain Diffusion-Weighted and Diffusion Tensor Imaging Findings in an Infant with Biotinidase Deficiency: Fig 1.;American Journal of Neuroradiology;2009-06-09