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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.Journal of Child Neurology|August 21, 2001
Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndromeM Cacić, E Wilichowski, V Mejaski-Bosnjak, et al.Annals of Neurology|August 1, 1996
Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotypeG C Korenke, S Fuchs, E Krasemann, et al.Journal of the Neurological Sciences|June 10, 1998
Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutationE Wilichowski, G C Korenke, W Ruitenbeek, et al.Pediatric Research|February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndromeE Wilichowski, A Grüters, K Kruse, et al.Mycoses|November 1, 1995
Cerebral Pseudallescheria mycosis after near-drowningR Rüchel, E WilichowskiThe Laryngoscope|February 27, 2001
Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathiesP Zwirner, E WilichowskiMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1983
[Effect of hyperbilirubinaemia on cerebellar development in Gunn rats]F HanefeldPageof 33