Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alexandre Fabre

Showing results (41-50 of 73) with videos related to

Pageof 8
Sort By:
American Journal of Medical Genetics. Part A|February 1, 2018
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two familiesAlexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 3, 2019
Clinical Aspects of STAT3 Gain-of-Function Germline Mutations: A Systematic ReviewAlexandre Fabre, Sarah Marchal, Vincent Barlogis, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
Journal of Pediatric Hematology/Oncology|May 7, 2008
FDG PET and evaluation of posttherapeutic residual tumors in pediatric oncology: preliminary experienceNicolas André, Alexandre Fabre, Cécile Colavolpe, et al.
Stem Cells International|July 9, 2019
Detection of Human Microchimerism following Allogeneic Cell Transplantation Using Droplet Digital PCRCatherine A Lombard, Alexandre Fabre, Jérôme Ambroise, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 11, 2019
Correlation Between Clinical Signs and High-resolution Manometry Data in ChildrenMarine Juzaud, Marie-Dominique Lamblin, Alexandre Fabre, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 27, 2009
Exclusion of EGFR, HRAS, DSP, JUP, CTNNB1, PLEC1, and EPPK1 as functional candidate genes in 7 families with syndromic diarrhoeaAlexandre Fabre, Bertrand Roquelaure, Caroline Lacoste, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 24, 2025
Clinical presentation, treatment, and outcome of children with primary intestinal lymphangiectasia: A national retrospective studyNoémie Goret, Cécile Lambe, Emmanuelle Ecochard-Dugelay, et al.
Clinics and Research in Hepatology and Gastroenterology|March 4, 2021
A novel mutation of PCSK1 responsible for PC1/3 deficiency in two siblingsRémi Duclaux-Loras, Patrice Bourgeois, Pierre-Marie Lavrut, et al.
The Journal of Pediatrics|July 19, 2022
Comparison of Endoscopic Dilatation and Heller's Myotomy for Treating Esophageal Achalasia in Children: A Multicenter StudyAudrey Nicolas, Madeleine Aumar, Léa Chantal Tran, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|February 1, 2018
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two familiesAlexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 3, 2019
Clinical Aspects of STAT3 Gain-of-Function Germline Mutations: A Systematic ReviewAlexandre Fabre, Sarah Marchal, Vincent Barlogis, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
Journal of Pediatric Hematology/Oncology|May 7, 2008
FDG PET and evaluation of posttherapeutic residual tumors in pediatric oncology: preliminary experienceNicolas André, Alexandre Fabre, Cécile Colavolpe, et al.
Stem Cells International|July 9, 2019
Detection of Human Microchimerism following Allogeneic Cell Transplantation Using Droplet Digital PCRCatherine A Lombard, Alexandre Fabre, Jérôme Ambroise, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 11, 2019
Correlation Between Clinical Signs and High-resolution Manometry Data in ChildrenMarine Juzaud, Marie-Dominique Lamblin, Alexandre Fabre, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 27, 2009
Exclusion of EGFR, HRAS, DSP, JUP, CTNNB1, PLEC1, and EPPK1 as functional candidate genes in 7 families with syndromic diarrhoeaAlexandre Fabre, Bertrand Roquelaure, Caroline Lacoste, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 24, 2025
Clinical presentation, treatment, and outcome of children with primary intestinal lymphangiectasia: A national retrospective studyNoémie Goret, Cécile Lambe, Emmanuelle Ecochard-Dugelay, et al.
Clinics and Research in Hepatology and Gastroenterology|March 4, 2021
A novel mutation of PCSK1 responsible for PC1/3 deficiency in two siblingsRémi Duclaux-Loras, Patrice Bourgeois, Pierre-Marie Lavrut, et al.
The Journal of Pediatrics|July 19, 2022
Comparison of Endoscopic Dilatation and Heller's Myotomy for Treating Esophageal Achalasia in Children: A Multicenter StudyAudrey Nicolas, Madeleine Aumar, Léa Chantal Tran, et al.
Pageof 8