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Pediatric Neurology|September 1, 1996
Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patientsG C Korenke, P J Pouwels, J Frahm, 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.Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1983
Electroencephalogram investigations of the disequilibrium syndrome during bicarbonate and acetate dialysisH Hampl, H W Klopp, N Michels, et al.Nephrologie|January 1, 1983
[Electro-encephalographic study of the disequilibrium syndrome during bicarbonate dialysis and acetate dialysis]H Hampl, H W Klopp, N Michels, et al.Annals of Neurology|May 19, 2001
Presence of Chlamydia pneumoniae DNA in the cerebral spinal fluid is a common phenomenon in a variety of neurological diseases and not restricted to multiple sclerosisJ Gieffers, D Pohl, J Treib, et al.Journal of Inherited Metabolic Disease|May 9, 2000
Enhanced lymphocyte proliferation in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglyceridesR B Pour, S Stöckler-Ipsiroglu, D H Hunneman, et al.Human Molecular Genetics|November 1, 1994
Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406T Martinsson, C Bjursell, H Stibler, et al.Journal of Chromatography|July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric populationG F Hoffmann, C K Seppel, B Holmes, et al.Journal of Pediatric Hematology/Oncology|January 4, 1998
Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young childrenJ W Herms, J Behnke, M Bergmann, 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.Pageof 15