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Clinics and Research in Hepatology and Gastroenterology
|
November 21, 2021
Endoscopic training during fellowship: A nationwide French study: Impact of theoretical courses and simulation-based training during fellowship
Aymeric Becq, Iradj Sobhani, Blandine Vauquelin, et al.
Brain : a Journal of Neurology
|
July 24, 2009
Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases
Pierre Labauge, Laetitia Horzinski, Xavier Ayrignac, et al.
Endoscopy
|
June 26, 2015
Endoscopic treatment of fistula after sleeve gastrectomy: results of a multicenter retrospective study
Dimitri Christophorou, Jean-Christophe Valats, Natalie Funakoshi, et al.
Bulletin Du Cancer
|
May 13, 2005
[Clinical Practice Guidelines 2004. Standards, Options and Recommendations for the management of patient with adenocarcinoma of the stomach: radiotherapy (therapeutic evaluation)]
Marc Ychou, Guillaume Gory-Delabaere, Pierre Blanc, et al.
Circulation. Genomic and Precision Medicine
|
November 12, 2025
Exploring <i>RBFOX2</i> Haploinsufficiency: A New Genetic Link to Hypoplastic Left Heart Syndrome
Clément Sauvestre, Amel Bouchatal, Claire Beneteau, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
June 17, 2019
Efficacy of Tumor Necrosis Factor Antagonist Treatment in Patients With Refractory Ulcerative Proctitis
Guillaume Pineton de Chambrun, Aurélien Amiot, Guillaume Bouguen, et al.
Ophthalmic Genetics
|
November 29, 2024
The phenotypic spectrum of <i>CEP250</i> gene variants
Cécile Courdier, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Haematologica
|
February 11, 2010
The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance
Patricia Aguilar-Martinez, Michael Bismuth, François Blanc, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2024
Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum
Véronique Pingault, Cécilia Neiva-Vaz, Judite de Oliveira, et al.
American Journal of Human Genetics
|
January 27, 2026
Dominant and recessive ATOH1 variants cause distinct neurodevelopmental disorders with hearing loss
Nicole Bertola, Eléonore Blondiaux, Madeleine Harion, et al.
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Search research articles
Search
Showing results (111-120 of 147) with videos related to
Sort By:
Page
of 15
Clinics and Research in Hepatology and Gastroenterology
|
November 21, 2021
Endoscopic training during fellowship: A nationwide French study: Impact of theoretical courses and simulation-based training during fellowship
Aymeric Becq, Iradj Sobhani, Blandine Vauquelin, et al.
Brain : a Journal of Neurology
|
July 24, 2009
Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases
Pierre Labauge, Laetitia Horzinski, Xavier Ayrignac, et al.
Endoscopy
|
June 26, 2015
Endoscopic treatment of fistula after sleeve gastrectomy: results of a multicenter retrospective study
Dimitri Christophorou, Jean-Christophe Valats, Natalie Funakoshi, et al.
Bulletin Du Cancer
|
May 13, 2005
[Clinical Practice Guidelines 2004. Standards, Options and Recommendations for the management of patient with adenocarcinoma of the stomach: radiotherapy (therapeutic evaluation)]
Marc Ychou, Guillaume Gory-Delabaere, Pierre Blanc, et al.
Circulation. Genomic and Precision Medicine
|
November 12, 2025
Exploring <i>RBFOX2</i> Haploinsufficiency: A New Genetic Link to Hypoplastic Left Heart Syndrome
Clément Sauvestre, Amel Bouchatal, Claire Beneteau, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
June 17, 2019
Efficacy of Tumor Necrosis Factor Antagonist Treatment in Patients With Refractory Ulcerative Proctitis
Guillaume Pineton de Chambrun, Aurélien Amiot, Guillaume Bouguen, et al.
Ophthalmic Genetics
|
November 29, 2024
The phenotypic spectrum of <i>CEP250</i> gene variants
Cécile Courdier, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Haematologica
|
February 11, 2010
The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance
Patricia Aguilar-Martinez, Michael Bismuth, François Blanc, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2024
Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum
Véronique Pingault, Cécilia Neiva-Vaz, Judite de Oliveira, et al.
American Journal of Human Genetics
|
January 27, 2026
Dominant and recessive ATOH1 variants cause distinct neurodevelopmental disorders with hearing loss
Nicole Bertola, Eléonore Blondiaux, Madeleine Harion, et al.
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of 15