Cerebral metabolic changes in biotinidase deficiency
Author:
Affiliation:
1. Department of Paediatrics; Düsseldorf Germany
2. ; Department of Radiology; Heinrich-Heine-University; Düsseldorf Germany
3. ; Department of Paediatrics; Heinrich-Heine-University; Moorenstrasse 5 Düsseldorf D-40225 Germany
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005307415289/fullpdf
Reference17 articles.
1. Normalisation of severe cranial CT scan abnormalities after biotin in a case of biotinidase deficiency;Bakker;Eur J Pediatr,1994
2. Spatial localization in NMR spectroscopy in vivo;Bottomley;Ann NY Acad Sci,1987
3. Reversal of brain atrophy with biotin treatment in biotinidase deficiency;Bousounis;Neuropediatrics,1993
4. Biotinidase deficiency: accumulation of lactate in the brain and response to physiologic doses of biotin;Diamantopoulos;Neurology,1986
5. Different organic acid patterns in urine and in cerebrospinal fluid in a patient with biotinidase deficiency;Di Rocco;J Inher Metab Dis,1984
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