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K Harzer

Showing results (11-20 of 126) with videos related to

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Zeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|January 1, 1984
[Fatal colchicine poisoning]K Harzer
Humangenetik|January 1, 1973
Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriersK Harzer
Klinische Wochenschrift|December 15, 1974
[Glucocerebrosidase deficiency and tentative identification of heterozygous carriers in a family with Gaucher's disease type I (author's transl)]K Harzer
Die Medizinische Welt|January 1, 1979
[Prenatal diagnosis of incurable familial metabolic diseases. Prenatal diagnosis of disorders of lipid metabolism]K Harzer
Journal of Neurochemistry|December 1, 1983
Sulfatides in prenatal metachromatic leukodystrophyW Baier, K Harzer
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1981
[Niemann-Pick disease type C (subacute neurovisceral lipidosis). Problems of altered sphingomyelinase activity in the brain (author's transl)]K Harzer, J Peiffer
Journal of Neural Transmission (Vienna, Austria : 1996)|July 28, 2001
On the role of peripheral macrophages during active experimental allergic encephalomyelitis (EAE)H Imrich, K Harzer
Journal of Chromatography|November 11, 1983
[Detection of intake of hashish in biological material]K Harzer, M Kächele
European Journal of Pediatrics|April 1, 1994
Bone marrow cytological storage phenomena in lipidosesS Ziyeh, K Harzer
Human Genetics|January 1, 1981
Genetic variation of hexosaminidase A and arylsulfatase A activity. Correlation study in amnio-maternal pairs of cultured cellsK Harzer, K Hayashi
Pageof 13

Showing results (11-20 of 126) with videos related to

Sort By:
Pageof 13
Zeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|January 1, 1984
[Fatal colchicine poisoning]K Harzer
Humangenetik|January 1, 1973
Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriersK Harzer
Klinische Wochenschrift|December 15, 1974
[Glucocerebrosidase deficiency and tentative identification of heterozygous carriers in a family with Gaucher's disease type I (author's transl)]K Harzer
Die Medizinische Welt|January 1, 1979
[Prenatal diagnosis of incurable familial metabolic diseases. Prenatal diagnosis of disorders of lipid metabolism]K Harzer
Journal of Neurochemistry|December 1, 1983
Sulfatides in prenatal metachromatic leukodystrophyW Baier, K Harzer
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1981
[Niemann-Pick disease type C (subacute neurovisceral lipidosis). Problems of altered sphingomyelinase activity in the brain (author's transl)]K Harzer, J Peiffer
Journal of Neural Transmission (Vienna, Austria : 1996)|July 28, 2001
On the role of peripheral macrophages during active experimental allergic encephalomyelitis (EAE)H Imrich, K Harzer
Journal of Chromatography|November 11, 1983
[Detection of intake of hashish in biological material]K Harzer, M Kächele
European Journal of Pediatrics|April 1, 1994
Bone marrow cytological storage phenomena in lipidosesS Ziyeh, K Harzer
Human Genetics|January 1, 1981
Genetic variation of hexosaminidase A and arylsulfatase A activity. Correlation study in amnio-maternal pairs of cultured cellsK Harzer, K Hayashi
Pageof 13