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Showing results (671-680 of 720) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 18, 2010
Cellular in vivo imaging reveals coordinated regulation of pituitary microcirculation and GH cell network functionChrystel Lafont, Michel G Desarménien, Mathieu Cassou, et al.
European Radiology|March 31, 2026
Improving membranous urethral length measurements on prostate MRI: a comparison of online training methodsElisabeth P Goedegebuure, Thierry N Boellaard, Margriet C van Dijk-de Haan, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
[Immuno-hemolytic transfusion reactions. III. Report of 61 cases]P Y Le Pennec, A M Tissier, L Mannessier, et al.
Surgery|November 14, 2018
NIFT-P: Are they indolent tumors? Results of a multi-institutional studyNathalie Chereau, Tristan Greilsamer, Eric Mirallié, et al.
American Journal of Human Genetics|June 11, 2019
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to AsthenozoospermiaMarjorie Whitfield, Lucie Thomas, Emilie Bequignon, et al.
Ebiomedicine|August 27, 2019
A new paradigm for lung-conservative total liquid ventilationMatthias Kohlhauer, Emilie Boissady, Fanny Lidouren, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2006
A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindredsLionel Groussin, Anelia Horvath, Eric Jullian, et al.
Thyroid : Official Journal of the American Thyroid Association|March 30, 2017
Molecular Pathology of Anaplastic Thyroid Carcinomas: A Retrospective Study of 144 CasesBenjamin Bonhomme, Yann Godbert, Gaelle Perot, et al.
American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Brain : a Journal of Neurology|January 4, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegiaJean-Loup Méreaux, Guillaume Banneau, Mélanie Papin, et al.
Pageof 72

Showing results (671-680 of 720) with videos related to

Sort By:
Pageof 72
Proceedings of the National Academy of Sciences of the United States of America|February 18, 2010
Cellular in vivo imaging reveals coordinated regulation of pituitary microcirculation and GH cell network functionChrystel Lafont, Michel G Desarménien, Mathieu Cassou, et al.
European Radiology|March 31, 2026
Improving membranous urethral length measurements on prostate MRI: a comparison of online training methodsElisabeth P Goedegebuure, Thierry N Boellaard, Margriet C van Dijk-de Haan, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
[Immuno-hemolytic transfusion reactions. III. Report of 61 cases]P Y Le Pennec, A M Tissier, L Mannessier, et al.
Surgery|November 14, 2018
NIFT-P: Are they indolent tumors? Results of a multi-institutional studyNathalie Chereau, Tristan Greilsamer, Eric Mirallié, et al.
American Journal of Human Genetics|June 11, 2019
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to AsthenozoospermiaMarjorie Whitfield, Lucie Thomas, Emilie Bequignon, et al.
Ebiomedicine|August 27, 2019
A new paradigm for lung-conservative total liquid ventilationMatthias Kohlhauer, Emilie Boissady, Fanny Lidouren, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2006
A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindredsLionel Groussin, Anelia Horvath, Eric Jullian, et al.
Thyroid : Official Journal of the American Thyroid Association|March 30, 2017
Molecular Pathology of Anaplastic Thyroid Carcinomas: A Retrospective Study of 144 CasesBenjamin Bonhomme, Yann Godbert, Gaelle Perot, et al.
American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Brain : a Journal of Neurology|January 4, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegiaJean-Loup Méreaux, Guillaume Banneau, Mélanie Papin, et al.
Pageof 72