Resolution of subependymal cysts in neonatal holocarboxylase synthetase deficiency
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1997.tb07424.x/fullpdf
Reference11 articles.
1. A new case of holocarboxylase synthetase deficiency;Briones;Journal of Inherited Metabolic Disease,1989
2. Leucoencéphalopathie familiale associée à une acidase lactique congénitale;Farkas;Acta Neuropathologica,1971
3. Holocarboxylase synthetase deficiency: early diagnosis and management of a new case;Fuchshuber;European Journal of Pediatrics,1992
4. Biotin-responsive β-methylerotonoylglycinuria;Gompertz;Lancet,1971
5. Neurological manifestations of organic aeid disorders;Hoffmann;European Journal of Pediatrics,1994
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