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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 PatonHuman Genetics|December 1, 1987
Prenatal enzymatic diagnosis and exclusion of Krabbe's disease (globoid-cell leukodystrophy) using chorionic villi in five risk pregnanciesK Harzer, H D Hager, G TariverdianDeutsche Medizinische Wochenschrift (1946)|May 15, 1981
[Prenatal diagnosis of Gaucher's disease (author's transl)]H Heilbronner, K G Wurster, K HarzerCleveland Clinic Journal of Medicine|January 1, 1989
Genetic aspects of childhood epilepsyH Doose, W BaierPageof 14