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Padiatrie Und Padologie|January 1, 1993
Diagnosis of peroxisomal disorders with neurological involvementB MolzerClinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1976
Detection of GM2-gangliosidosis (Tay-Sachs and Sandhoff disease) gene carriers by serum hexosaminidase assayB Molzer, H BernheimerKlinische Padiatrie|March 1, 1986
[Lipid storage diseases (lipidoses): genetic, biochemical and clinico-chemical aspects]H Bernheimer, B MolzerWiener Klinische Wochenschrift|January 1, 1992
[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]B Molzer, S Stöckler, H BernheimerActa Neuropathologica. Supplementum|January 1, 1981
Fatty acid patterns in brain, fibroblast, leukocyte and body fluid lipids in adrenoleukodystrophyB Molzer, H Bernheimer, K ToiflBiochemical and Biophysical Research Communications|December 30, 1994
X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypesJ Berger, B Molzer, I Faé, et al.Human Genetics|October 1, 1993
Simultaneous detection of the two most frequent metachromatic leukodystrophy mutationsJ Berger, B Molzer, V Gieselmann, et al.Human Molecular Genetics|November 7, 2000
Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophyG Unterrainer, B Molzer, S Forss-Petter, et al.Human Mutation|January 15, 1999
Coincidence of two novel arylsulfatase A alleles and mutation 459+1G>A within a family with metachromatic leukodystrophy: molecular basis of phenotypic heterogeneityJ Berger, M Gmach, U Mayr, et al.American Journal of Medical Genetics|November 1, 1992
Elevated sulfatide excretion in heterozygotes of metachromatic leukodystrophy: dependence on reduction of arylsulfatase A activityB Molzer, R Sundt-Heller, M Kainz-Korschinsky, et al.Pageof 4