Showing results (81-90 of 143) with videos related to
Sort By:
Pageof 15
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferaseC Körner, R Knauer, U Holzbach, et al.Neuropediatrics|February 7, 2003
Successful management of drooling with botulinum toxin A in neurologically disabled childrenM Ellies, S Rohrbach-Volland, C Arglebe, et al.Metabolism: Clinical and Experimental|October 10, 1997
Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesisS Stöckler, B Marescau, P P De Deyn, et al.Neuropediatrics|October 1, 1993
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopyF Hanefeld, U Holzbach, B Kruse, et al.Human Genetics|February 1, 1996
Identification of mutations in the ALD-gene of 20 families with adrenoleukodystrophy/adrenomyeloneuropathyE W Krasemann, V Meier, G C Korenke, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crisesG C Korenke, H J Christen, K Hyland, et al.Artificial Organs|November 1, 1982
Advantages of bicarbonate hemodialysisH Hampl, H Klopp, M Wolfgruber, et al.Brain & Development|November 1, 1991
Multiple sclerosis in childhood: report of 15 casesF Hanefeld, H J Bauer, H J Christen, et al.Pediatric Neurology|August 30, 2000
Quantitative proton magnetic resonance spectroscopy of focal brain lesionsB Wilken, P Dechent, J Herms, et al.Journal of Medical Genetics|December 24, 1998
Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28T Webb, A Clarke, F Hanefeld, et al.Pageof 15