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K Harzer

Showing results (41-50 of 126) with videos related to

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American 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 Baumann
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1982
[Ultrastructural findings in 9 fetuses following prenatal diagnosis of neurolipidoses]G Suchlandt, W Schlote, K Harzer
European Journal of Pediatrics|April 1, 1997
Hydrops fetalis: manifestation in lysosomal storage diseases including Farber diseaseE Kattner, A Schäfer, K Harzer
Ultrastructural 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 Schlote
FEBS Letters|November 15, 2001
Saposins (sap) A and C activate the degradation of galactosylsphingosineK Harzer, M Hiraiwa, B C Paton
Human 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 Tariverdian
Journal of Neurochemistry|December 1, 1977
Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction-dependent: evidence for a component defect in Niemann-Pick disease type C is spuriousK Harzer, A P Anzil, I Schuster
Deutsche Medizinische Wochenschrift (1946)|May 15, 1981
[Prenatal diagnosis of Gaucher's disease (author's transl)]H Heilbronner, K G Wurster, K Harzer
European Journal of Pediatrics|August 1, 1995
A family with combined Farber and Sandhoff, isolated Sandhoff and isolated fetal Farber disease: postnatal exclusion and prenatal diagnosis of Farber disease using lipid loading tests on intact cultured cellsT Levade, H Enders, M Schliephacke, et al.
Journal of Neurochemistry|December 1, 1971
Enzyme alterations and lipid storage in three variants of Tay-Sachs diseaseK Sandhoff, K Harzer, W Wässle, et al.
Pageof 13

Showing results (41-50 of 126) with videos related to

Sort By:
Pageof 13
American 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 Baumann
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1982
[Ultrastructural findings in 9 fetuses following prenatal diagnosis of neurolipidoses]G Suchlandt, W Schlote, K Harzer
European Journal of Pediatrics|April 1, 1997
Hydrops fetalis: manifestation in lysosomal storage diseases including Farber diseaseE Kattner, A Schäfer, K Harzer
Ultrastructural 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 Schlote
FEBS Letters|November 15, 2001
Saposins (sap) A and C activate the degradation of galactosylsphingosineK Harzer, M Hiraiwa, B C Paton
Human 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 Tariverdian
Journal of Neurochemistry|December 1, 1977
Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction-dependent: evidence for a component defect in Niemann-Pick disease type C is spuriousK Harzer, A P Anzil, I Schuster
Deutsche Medizinische Wochenschrift (1946)|May 15, 1981
[Prenatal diagnosis of Gaucher's disease (author's transl)]H Heilbronner, K G Wurster, K Harzer
European Journal of Pediatrics|August 1, 1995
A family with combined Farber and Sandhoff, isolated Sandhoff and isolated fetal Farber disease: postnatal exclusion and prenatal diagnosis of Farber disease using lipid loading tests on intact cultured cellsT Levade, H Enders, M Schliephacke, et al.
Journal of Neurochemistry|December 1, 1971
Enzyme alterations and lipid storage in three variants of Tay-Sachs diseaseK Sandhoff, K Harzer, W Wässle, et al.
Pageof 13