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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
March 29, 2026
Development and external validation of a predictive model for postoperative recurrence of Crohn's disease in the biologic era
Matthieu Allez, Michiel T J Bak, Sofia Brand, et al.
Elife
|
August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune function
Mengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Gastroenterology
|
March 23, 2002
Terlipressin in patients with cirrhosis and type 1 hepatorenal syndrome: a retrospective multicenter study
Richard Moreau, Francois Durand, Thierry Poynard, et al.
The Lancet Regional Health. Europe
|
November 24, 2025
Management and survival of patients with cancer of unknown primary discussed by a French national multidisciplinary tumour board: a retrospective analysis
Célia Dupain, Nicolas Jacquin, Aurélien Latouche, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
Saturation genome editing of <i>RNU4-2</i> reveals distinct dominant and recessive neurodevelopmental disorders
Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, et al.
American Journal of Human Genetics
|
April 13, 2023
Bi-allelic variants in INTS11 are associated with a complex neurological disorder
Burak Tepe, Erica L Macke, Marcello Niceta, et al.
European Journal of Human Genetics : EJHG
|
April 4, 2025
Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features
Christel Thauvin-Robinet, Aurore Garde, Maud Favier, et al.
Nature
|
April 8, 2026
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders
Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, et al.
European Journal of Human Genetics : EJHG
|
June 25, 2025
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization
Camille Engel, Michaela Rendek, Jessica Assoumani, et al.
American Journal of Human Genetics
|
October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway
Maolei Gong, Jiayi Li, Zailong Qin, et al.
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of 15
Search research articles
Search
Showing results (131-140 of 147) with videos related to
Sort By:
Page
of 15
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
March 29, 2026
Development and external validation of a predictive model for postoperative recurrence of Crohn's disease in the biologic era
Matthieu Allez, Michiel T J Bak, Sofia Brand, et al.
Elife
|
August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune function
Mengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Gastroenterology
|
March 23, 2002
Terlipressin in patients with cirrhosis and type 1 hepatorenal syndrome: a retrospective multicenter study
Richard Moreau, Francois Durand, Thierry Poynard, et al.
The Lancet Regional Health. Europe
|
November 24, 2025
Management and survival of patients with cancer of unknown primary discussed by a French national multidisciplinary tumour board: a retrospective analysis
Célia Dupain, Nicolas Jacquin, Aurélien Latouche, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
Saturation genome editing of <i>RNU4-2</i> reveals distinct dominant and recessive neurodevelopmental disorders
Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, et al.
American Journal of Human Genetics
|
April 13, 2023
Bi-allelic variants in INTS11 are associated with a complex neurological disorder
Burak Tepe, Erica L Macke, Marcello Niceta, et al.
European Journal of Human Genetics : EJHG
|
April 4, 2025
Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features
Christel Thauvin-Robinet, Aurore Garde, Maud Favier, et al.
Nature
|
April 8, 2026
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders
Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, et al.
European Journal of Human Genetics : EJHG
|
June 25, 2025
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization
Camille Engel, Michaela Rendek, Jessica Assoumani, et al.
American Journal of Human Genetics
|
October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway
Maolei Gong, Jiayi Li, Zailong Qin, et al.
Page
of 15