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K Fink

Showing results (191-200 of 363) with videos related to

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Neurotoxicology|September 8, 2009
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zincPeter Hedera, Amanda Peltier, John K Fink, et al.
Archives of Neurology|September 1, 1991
Clinical and genetic analysis of progressive dystonia with diurnal variationJ K Fink, P D Ravin, M Filling-Katz, et al.
Neurology|May 1, 1988
Dystonia with marked diurnal variation associated with biopterin deficiencyJ K Fink, N Barton, W Cohen, et al.
Behavioural Brain Research|January 1, 1996
Presynaptic 5-HT auto- and heteroreceptors in the human central and peripheral nervous systemM Göthert, K Fink, D Frölich, et al.
Neurology|August 1, 1988
Multiple sulfatase deficiencyB W Soong, A C Casamassima, J K Fink, et al.
Physical Chemistry Chemical Physics : PCCP|February 16, 2017
Stripping off hydrogens in imidazole triggered by the attachment of a single electronA Ribar, K Fink, Z Li, et al.
Neurology|July 17, 1999
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8qP Hedera, S DiMauro, E Bonilla, et al.
Arzneimittel-Forschung|January 1, 1983
[Pharmacology of potential antidepressants of the N-L-phenylalanyl-beta-phenylalkylamine class]D Beck, K Fink, J Hölzl, et al.
Deutsche Medizinische Wochenschrift (1946)|February 12, 1998
[Acute renal failure in IgM plasmocytoma with hyperviscosity syndrome]M Nitschke, K Fink, S Pawlow-Handt, et al.
The Journal of Clinical Investigation|October 1, 1974
Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiencyW N Valentine, K Fink, D E Paglia, et al.
Pageof 37

Showing results (191-200 of 363) with videos related to

Sort By:
Pageof 37
Neurotoxicology|September 8, 2009
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zincPeter Hedera, Amanda Peltier, John K Fink, et al.
Archives of Neurology|September 1, 1991
Clinical and genetic analysis of progressive dystonia with diurnal variationJ K Fink, P D Ravin, M Filling-Katz, et al.
Neurology|May 1, 1988
Dystonia with marked diurnal variation associated with biopterin deficiencyJ K Fink, N Barton, W Cohen, et al.
Behavioural Brain Research|January 1, 1996
Presynaptic 5-HT auto- and heteroreceptors in the human central and peripheral nervous systemM Göthert, K Fink, D Frölich, et al.
Neurology|August 1, 1988
Multiple sulfatase deficiencyB W Soong, A C Casamassima, J K Fink, et al.
Physical Chemistry Chemical Physics : PCCP|February 16, 2017
Stripping off hydrogens in imidazole triggered by the attachment of a single electronA Ribar, K Fink, Z Li, et al.
Neurology|July 17, 1999
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8qP Hedera, S DiMauro, E Bonilla, et al.
Arzneimittel-Forschung|January 1, 1983
[Pharmacology of potential antidepressants of the N-L-phenylalanyl-beta-phenylalkylamine class]D Beck, K Fink, J Hölzl, et al.
Deutsche Medizinische Wochenschrift (1946)|February 12, 1998
[Acute renal failure in IgM plasmocytoma with hyperviscosity syndrome]M Nitschke, K Fink, S Pawlow-Handt, et al.
The Journal of Clinical Investigation|October 1, 1974
Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiencyW N Valentine, K Fink, D E Paglia, et al.
Pageof 37