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Clinical Genetics|November 1, 1996
Late juvenile metachromatic leukodystrophy (MLD) in three patients with a similar clinical course and identical mutation on one alleleA Tylki-Szymanska, J Berger, B Löschl, et al.Wiener Klinische Wochenschrift|December 8, 1978
[Mucopolysaccharidosis V (Ullrich-Scheie syndrome) (author's transl)]J Kovarik, W Vormittag, W Gebhart, et al.Pediatric Research|September 1, 1985
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detectionA Roscher, B Molzer, H Bernheimer, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|November 30, 1986
Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variantsB Molzer, M Korschinsky, H Bernheimer, et al.Human Molecular Genetics|April 10, 1999
Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapyA Netik, S Forss-Petter, A Holzinger, et al.Journal of Inherited Metabolic Disease|October 14, 2000
Rolipram does not normalize very long-chain fatty acid levels in adrenoleukodystrophy protein-deficient fibroblasts and miceA Netik, A Hobel, H Rauschka, et al.Fortschritte Der Neurologie, Psychiatrie, Und Ihrer Grenzgebiete|February 1, 1979
[Clinical and biochemical follow up of Refsum's disease (author's transl)]G S Barolin, E Hodkewitsch, E Höfinger, et al.European Neurology|January 1, 1993
Multiple sclerosis-like syndrome in a woman heterozygous for adrenoleukodystrophyS Stöckler, M Millner, B Molzer, et al.Clinical Genetics|June 15, 2005
Molecular and phenotypic characteristics of metachromatic leukodystrophy patients from PolandA Ługowska, J Berger, A Tylki-Szymańska, et al.Biochemical and Biophysical Research Communications|November 13, 1995
Association of X-linked adrenoleukodystrophy with HLA DRB1 allelesJ Berger, H Bernheimer, I Faé, et al.Pageof 4