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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.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.Cytogenetics and Cell Genetics|February 15, 2001
Molecular evolution of the murine tspy genesS Schubert, F Dechend, B Skawran, et al.Biochimica Et Biophysica Acta|May 9, 2001
Electrospray ionization mass spectrometry, circular dichroism and SAXS studies of the (S)-hydroxynitrile lyase from Hevea brasiliensisU Hanefeld, G Stranzl, A J Straathof, et al.Human Genetics|January 1, 1984
Mean corpuscular hemoglobin is increased in Martin-Bell syndromeU Langenbeck, J Schmidtke, I Bartels, et al.Human Genetics|February 1, 1991
A novel human multi-locus DNA family detected by pJU78 (DF31)F Peinemann, D N Cooper, K H Grzeschik, et al.Journal of Medical Genetics|October 1, 1991
A cystic fibrosis patient homozygous for the nonsense mutation R553XJ Bal, M Stuhrmann, M Schloesser, et al.Pageof 33