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Lars Hansen

Showing results (61-70 of 178) with videos related to

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Brain Research. Molecular Brain Research|July 14, 2004
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patientsMads Bak, Claus Hansen, Karen Friis Henriksen, et al.
International Journal of Psychiatry in Clinical Practice|December 10, 2022
Dopamine partial agonists: a discrete class of antipsychoticsDavid Taylor, Ramalingam Chithiramohan, Jasdev Grewal, et al.
Journal of Experimental Orthopaedics|June 7, 2017
Dynamic radiostereometric analysis for evaluation of hip joint pathomechanicsLars Hansen, Sepp de Raedt, Peter Bo Jørgensen, et al.
The Journal of Clinical Psychiatry|April 25, 2009
Akathisia: an updated review focusing on second-generation antipsychoticsJohn M Kane, Wolfgang W Fleischhacker, Lars Hansen, et al.
BMJ (Clinical Research Ed.)|February 3, 2007
Schizophrenia can and should be renamedDavid G Kingdon, Yoshihiro Kinoshita, Farooq Naeem, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8Lars Hansen, Wenliang Yao, Hans Eiberg, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2006
The Pro12Ala variant of the PPARG gene is a risk factor for peroxisome proliferator-activated receptor-gamma/alpha agonist-induced edema in type 2 diabetic patientsLars Hansen, Claus T Ekstrøm, René Tabanera Y Palacios, et al.
British Journal of Clinical Pharmacology|May 9, 2025
Pharmacokinetic-pharmacodynamic (PK/PD) modelling of cotadutide effect in patients with chronic kidney disease and type 2 diabetes mellitusHongtao Yu, Victoria Parker, Viknesh Selvarajah, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor geneHans Eiberg, Josephine B Olsson, Mads Bak, et al.
Human Genetics|January 4, 2008
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expressionHans Eiberg, Jesper Troelsen, Mette Nielsen, et al.
Pageof 18

Showing results (61-70 of 178) with videos related to

Sort By:
Pageof 18
Brain Research. Molecular Brain Research|July 14, 2004
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patientsMads Bak, Claus Hansen, Karen Friis Henriksen, et al.
International Journal of Psychiatry in Clinical Practice|December 10, 2022
Dopamine partial agonists: a discrete class of antipsychoticsDavid Taylor, Ramalingam Chithiramohan, Jasdev Grewal, et al.
Journal of Experimental Orthopaedics|June 7, 2017
Dynamic radiostereometric analysis for evaluation of hip joint pathomechanicsLars Hansen, Sepp de Raedt, Peter Bo Jørgensen, et al.
The Journal of Clinical Psychiatry|April 25, 2009
Akathisia: an updated review focusing on second-generation antipsychoticsJohn M Kane, Wolfgang W Fleischhacker, Lars Hansen, et al.
BMJ (Clinical Research Ed.)|February 3, 2007
Schizophrenia can and should be renamedDavid G Kingdon, Yoshihiro Kinoshita, Farooq Naeem, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8Lars Hansen, Wenliang Yao, Hans Eiberg, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2006
The Pro12Ala variant of the PPARG gene is a risk factor for peroxisome proliferator-activated receptor-gamma/alpha agonist-induced edema in type 2 diabetic patientsLars Hansen, Claus T Ekstrøm, René Tabanera Y Palacios, et al.
British Journal of Clinical Pharmacology|May 9, 2025
Pharmacokinetic-pharmacodynamic (PK/PD) modelling of cotadutide effect in patients with chronic kidney disease and type 2 diabetes mellitusHongtao Yu, Victoria Parker, Viknesh Selvarajah, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor geneHans Eiberg, Josephine B Olsson, Mads Bak, et al.
Human Genetics|January 4, 2008
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expressionHans Eiberg, Jesper Troelsen, Mette Nielsen, et al.
Pageof 18