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Human Genetics|January 1, 1983
Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymogramsB Kustermann-Kuhn, K HarzerClinica Chimica Acta; International Journal of Clinical Chemistry|March 16, 2001
Quantified increases of cholesterol, total lipid and globotriaosylceramide in filipin-positive Niemann-Pick type C fibroblastsK Harzer, B Kustermann-KuhnAJNR. American Journal of Neuroradiology|June 28, 2000
The influence of gliomas and nonglial space-occupying lesions on blood-oxygen-level-dependent contrast enhancementA Schreiber, U Hubbe, S Ziyeh, et al.Neuropediatrics|May 1, 1984
Diffuse-disseminated sclerosis combined with partial arylsulfatase A (ASA) deficiency. Mixed heterozygosity of ASA- and pseudo-ASA-deficiency?J Peiffer, K Harzer, W SchloteMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1981
[Infantile and late-onset type of globoid cell leucodystrophy in one family (author's transl)]H Böhles, R Schlenk, K HarzerAmerican Journal of Human Genetics|March 1, 1977
Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy familyG Dubois, K Harzer, N BaumannArchiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1982
[Ultrastructural findings in 9 fetuses following prenatal diagnosis of neurolipidoses]G Suchlandt, W Schlote, K HarzerEuropean Journal of Pediatrics|April 1, 1997
Hydrops fetalis: manifestation in lysosomal storage diseases including Farber diseaseE Kattner, A Schäfer, K HarzerUltrastructural Pathology|November 9, 2006
Variations of the ultrastructure of neuronal lipofuscin during childhood and adolescence in the human Ammon's hornJ W Boellaard, K Harzer, W SchloteFEBS Letters|November 15, 2001
Saposins (sap) A and C activate the degradation of galactosylsphingosineK Harzer, M Hiraiwa, B C PatonPageof 11