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H W Goedde

Showing results (201-210 of 269) with videos related to

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Humangenetik|January 1, 1971
New biochemical and immunological data on quantitative and qualitative variability of human pseudocholinesteraseK Altland, H W Goedde, K Held, et al.
Archives of Neurology|March 1, 1981
Hereditary ataxia and the sixth chromosomeA H Koeppen, H W Goedde, C Hiller, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
A case of Lesch Nyhan syndrome with delayed onset of self-mutilation: search for abnormal biochemical, immunological and cell growth characteristic in fibroblasts and neurotransmitters in urineS Singh, I Willers, K Ullrich, et al.
MMW, Munchener Medizinische Wochenschrift|July 13, 1979
[Perforating sigmoid diverticulitis in monozygotic twins]H H Pusch, G Börger, L Hirth, et al.
Lancet (London, England)|January 12, 1980
Genetic linkage in hereditary ataxiaA H Koeppen, H W Goedde, L Hirth, et al.
Progress in Clinical and Biological Research|January 1, 1989
"High Km" aldehyde dehydrogenase isozymes in human tissues: constitutive and tumor-associated formsD P Agarwal, R Eckey, A C Rudnay, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
Human liver glutamic gamma-semialdehyde dehydrogenase: structural relationship to the yeast enzymeJ Hempel, R Eckey, D Berie, et al.
Humangenetik|January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in FinlandS Singh, M Jensen, H W Goedde, et al.
Human Heredity|January 1, 1974
Phenotypes of Gc and Tf in leprosy patients of Mali and EthiopiaH W Goedde, H G Benkmann, L Hirth, et al.
Human Genetics|January 1, 1981
A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: comparison with erythrocyte activityJ J Hoo, T Strohmeyer, W J Beckermann, et al.
Pageof 27

Showing results (201-210 of 269) with videos related to

Sort By:
Pageof 27
Humangenetik|January 1, 1971
New biochemical and immunological data on quantitative and qualitative variability of human pseudocholinesteraseK Altland, H W Goedde, K Held, et al.
Archives of Neurology|March 1, 1981
Hereditary ataxia and the sixth chromosomeA H Koeppen, H W Goedde, C Hiller, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
A case of Lesch Nyhan syndrome with delayed onset of self-mutilation: search for abnormal biochemical, immunological and cell growth characteristic in fibroblasts and neurotransmitters in urineS Singh, I Willers, K Ullrich, et al.
MMW, Munchener Medizinische Wochenschrift|July 13, 1979
[Perforating sigmoid diverticulitis in monozygotic twins]H H Pusch, G Börger, L Hirth, et al.
Lancet (London, England)|January 12, 1980
Genetic linkage in hereditary ataxiaA H Koeppen, H W Goedde, L Hirth, et al.
Progress in Clinical and Biological Research|January 1, 1989
"High Km" aldehyde dehydrogenase isozymes in human tissues: constitutive and tumor-associated formsD P Agarwal, R Eckey, A C Rudnay, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
Human liver glutamic gamma-semialdehyde dehydrogenase: structural relationship to the yeast enzymeJ Hempel, R Eckey, D Berie, et al.
Humangenetik|January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in FinlandS Singh, M Jensen, H W Goedde, et al.
Human Heredity|January 1, 1974
Phenotypes of Gc and Tf in leprosy patients of Mali and EthiopiaH W Goedde, H G Benkmann, L Hirth, et al.
Human Genetics|January 1, 1981
A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: comparison with erythrocyte activityJ J Hoo, T Strohmeyer, W J Beckermann, et al.
Pageof 27