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W Friedl

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Arteriosclerosis (Dallas, Tex.)|January 1, 1990
Association of DNA polymorphism at the apolipoprotein B gene locus with coronary heart disease and serum very low density lipoprotein levelsB Paulweber, W Friedl, F Krempler, et al.
Journal of Neurology|April 29, 2000
Involvement of the visual pathway in hereditary neuropathy with liability to pressure palsiesC Schneider, K Reiners, W Friedl, et al.
Journal of Neurochemistry|December 1, 1988
Limited tryptic proteolysis of the benzodiazepine binding proteins in different species reveals structural homologiesW Friedl, K U Lentes, E Schmitz, et al.
Zeitschrift Fur Gastroenterologie|November 1, 1985
[I.v. famotidine versus i.v. ranitidine: intragastric pH behavior in surgical intensive care patients]W Friedl, C Krier, H G Dammann, et al.
Acta Psychiatrica Scandinavica|August 1, 1981
Low platelet MAO activity and schizophrenia: sex differencesW F Gattaz, S Kasper, P Propping, et al.
American Journal of Medical Genetics|December 23, 1999
ADULT syndrome allelic to limb mammary syndrome (LMS)?P Propping, W Friedl, T F Wienker, et al.
Atherosclerosis|October 1, 1988
Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart diseaseB Paulweber, W Friedl, F Krempler, et al.
Human Genetics|January 1, 1981
Quantitative and qualitative assay of amniotic-fluid acetylcholinesterase in the prenatal diagnosis of neural tube defectsT Voigtländer, W Friedl, M Cremer, et al.
The American Journal of Gastroenterology|November 6, 2001
A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardationJ Raedle, W Friedl, H Engels, et al.
Human Molecular Genetics|June 1, 1994
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosisM Mandl, M Kadmon, M Sengteller, et al.
Pageof 20

Showing results (111-120 of 194) with videos related to

Sort By:
Pageof 20
Arteriosclerosis (Dallas, Tex.)|January 1, 1990
Association of DNA polymorphism at the apolipoprotein B gene locus with coronary heart disease and serum very low density lipoprotein levelsB Paulweber, W Friedl, F Krempler, et al.
Journal of Neurology|April 29, 2000
Involvement of the visual pathway in hereditary neuropathy with liability to pressure palsiesC Schneider, K Reiners, W Friedl, et al.
Journal of Neurochemistry|December 1, 1988
Limited tryptic proteolysis of the benzodiazepine binding proteins in different species reveals structural homologiesW Friedl, K U Lentes, E Schmitz, et al.
Zeitschrift Fur Gastroenterologie|November 1, 1985
[I.v. famotidine versus i.v. ranitidine: intragastric pH behavior in surgical intensive care patients]W Friedl, C Krier, H G Dammann, et al.
Acta Psychiatrica Scandinavica|August 1, 1981
Low platelet MAO activity and schizophrenia: sex differencesW F Gattaz, S Kasper, P Propping, et al.
American Journal of Medical Genetics|December 23, 1999
ADULT syndrome allelic to limb mammary syndrome (LMS)?P Propping, W Friedl, T F Wienker, et al.
Atherosclerosis|October 1, 1988
Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart diseaseB Paulweber, W Friedl, F Krempler, et al.
Human Genetics|January 1, 1981
Quantitative and qualitative assay of amniotic-fluid acetylcholinesterase in the prenatal diagnosis of neural tube defectsT Voigtländer, W Friedl, M Cremer, et al.
The American Journal of Gastroenterology|November 6, 2001
A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardationJ Raedle, W Friedl, H Engels, et al.
Human Molecular Genetics|June 1, 1994
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosisM Mandl, M Kadmon, M Sengteller, et al.
Pageof 20