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A Frisch

Showing results (31-40 of 81) with videos related to

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Die Pharmazie|March 21, 2024
A comprehensive study of prescribing, administering and drug handling medication errors in ten wards of a university hospital after implementation of electronic prescribing, clinical pharmacists or medication reconciliationJ Schuster, A Saddawi, A Frisch, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriersL Peleg, A Frisch, B Goldman, et al.
Molecular Psychiatry|March 24, 1999
A novel allele in the promoter region of the human serotonin transporter geneE Michaelovsky, A Frisch, R Rockah, et al.
American Journal of Human Genetics|January 1, 1985
Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX AR Navon, R Kopel, J Nutman, et al.
Scandinavian Journal of Medicine & Science in Sports|November 13, 2008
Analysis of sex-specific injury patterns and risk factors in young high-level athletesA Frisch, R Seil, A Urhausen, et al.
Molecular Psychiatry|May 1, 1997
No association between the serotonin transporter gene regulatory region polymorphism and the Tridimensional Personality Questionnaire (TPQ) temperament of harm avoidanceR P Ebstein, I Gritsenko, L Nemanov, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 10, 2003
Modeling open-set spoken word recognition in postlingually deafened adults after cochlear implantation: some preliminary results with the neighborhood activation modelTed A Meyer, Stefan A Frisch, David B Pisoni, et al.
Vox Sanguinis|September 24, 2010
Influence of late irradiation on the in vitro RBC storage variables of leucoreduced RBCs in SAGM additive solutionR Zimmermann, A M Schoetz, A Frisch, et al.
American Journal of Medical Genetics|July 24, 1998
Linkage disequilibrium of common Gaucher disease mutations with a polymorphic site in the pyruvate kinase (PKLR) geneR Rockah, R Narinsky, M Frydman, et al.
Israel Journal of Medical Sciences|October 1, 1992
The autosomal dominant polycystic kidney disease gene in a Jewish family from Uzbekistan is PKD1A Frisch, M Frydman, O Blau, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
Die Pharmazie|March 21, 2024
A comprehensive study of prescribing, administering and drug handling medication errors in ten wards of a university hospital after implementation of electronic prescribing, clinical pharmacists or medication reconciliationJ Schuster, A Saddawi, A Frisch, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriersL Peleg, A Frisch, B Goldman, et al.
Molecular Psychiatry|March 24, 1999
A novel allele in the promoter region of the human serotonin transporter geneE Michaelovsky, A Frisch, R Rockah, et al.
American Journal of Human Genetics|January 1, 1985
Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX AR Navon, R Kopel, J Nutman, et al.
Scandinavian Journal of Medicine & Science in Sports|November 13, 2008
Analysis of sex-specific injury patterns and risk factors in young high-level athletesA Frisch, R Seil, A Urhausen, et al.
Molecular Psychiatry|May 1, 1997
No association between the serotonin transporter gene regulatory region polymorphism and the Tridimensional Personality Questionnaire (TPQ) temperament of harm avoidanceR P Ebstein, I Gritsenko, L Nemanov, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 10, 2003
Modeling open-set spoken word recognition in postlingually deafened adults after cochlear implantation: some preliminary results with the neighborhood activation modelTed A Meyer, Stefan A Frisch, David B Pisoni, et al.
Vox Sanguinis|September 24, 2010
Influence of late irradiation on the in vitro RBC storage variables of leucoreduced RBCs in SAGM additive solutionR Zimmermann, A M Schoetz, A Frisch, et al.
American Journal of Medical Genetics|July 24, 1998
Linkage disequilibrium of common Gaucher disease mutations with a polymorphic site in the pyruvate kinase (PKLR) geneR Rockah, R Narinsky, M Frydman, et al.
Israel Journal of Medical Sciences|October 1, 1992
The autosomal dominant polycystic kidney disease gene in a Jewish family from Uzbekistan is PKD1A Frisch, M Frydman, O Blau, et al.
Pageof 9