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Alexandre Fabre

Showing results (31-40 of 73) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|December 28, 2016
IBD-Like Features in Syndromic Diarrhea/Trichohepatoenteric SyndromeVeronica B Busoni, Julie Lemale, Beatrice Dubern, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 14, 2020
Child with liver transplant recovers from COVID-19 infection. A case reportAurélie Morand, Bertrand Roquelaure, Philippe Colson, et al.
European Journal of Medical Genetics|September 8, 2021
Deep phenotyping of MARS1 (interstitial lung and liver disease) and LARS1 (infantile liver failure syndrome 1) recessive multisystemic disease using Human Phenotype Ontology annotation: Overlap and differences. Case report and review of literatureCharlotte La Fay, Celia Hoebeke, Marine Juzaud, et al.
Plos Biology|June 9, 2020
Why and when was lactase persistence selected for? Insights from Central Asian herders and ancient DNALaure Segurel, Perle Guarino-Vignon, Nina Marchi, et al.
European Journal of Medical Genetics|July 6, 2019
Congenital Sodium Diarrhea by mutation of the SLC9A3 geneGeorges Dimitrov, Sarah Bamberger, Chloe Navard, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|December 16, 2014
Antioxidant potential is correlated to ω6 / ω3 ratio and Brasfield score in cystic fibrosis childrenAlexandre Fabre, Sylvie Caspar-Bauguil, Jean Gaudart, et al.
Orphanet Journal of Rare Diseases|August 18, 2021
Quality of life of transplanted children and their parents: a cross-sectional studyPauline Duvant, Magali Fillat, Florentine Garaix, et al.
European Journal of Medical Genetics|November 28, 2017
Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel diseaseJoão Farela Neves, Isabel Afonso, Luis Borrego, et al.
Annales De Pathologie|February 14, 2012
[Vasoactive intestinal polypeptide-secreting diffuse ganglioneuromatosis affecting the small intestine and the colon in an infant: an exceptional inaugural manifestation of NF1]Malik Kadri, Alexandre Fabre, Carole Coze, et al.
Annales De Pathologie|January 4, 2022
[Diagnosis of a rare and severe inflammatory bowel disease in an infant with peri-orificial ulcerations]Alexandre Bardet, Florence Riccardi, Julia Torrents, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Journal of Pediatric Gastroenterology and Nutrition|December 28, 2016
IBD-Like Features in Syndromic Diarrhea/Trichohepatoenteric SyndromeVeronica B Busoni, Julie Lemale, Beatrice Dubern, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 14, 2020
Child with liver transplant recovers from COVID-19 infection. A case reportAurélie Morand, Bertrand Roquelaure, Philippe Colson, et al.
European Journal of Medical Genetics|September 8, 2021
Deep phenotyping of MARS1 (interstitial lung and liver disease) and LARS1 (infantile liver failure syndrome 1) recessive multisystemic disease using Human Phenotype Ontology annotation: Overlap and differences. Case report and review of literatureCharlotte La Fay, Celia Hoebeke, Marine Juzaud, et al.
Plos Biology|June 9, 2020
Why and when was lactase persistence selected for? Insights from Central Asian herders and ancient DNALaure Segurel, Perle Guarino-Vignon, Nina Marchi, et al.
European Journal of Medical Genetics|July 6, 2019
Congenital Sodium Diarrhea by mutation of the SLC9A3 geneGeorges Dimitrov, Sarah Bamberger, Chloe Navard, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|December 16, 2014
Antioxidant potential is correlated to ω6 / ω3 ratio and Brasfield score in cystic fibrosis childrenAlexandre Fabre, Sylvie Caspar-Bauguil, Jean Gaudart, et al.
Orphanet Journal of Rare Diseases|August 18, 2021
Quality of life of transplanted children and their parents: a cross-sectional studyPauline Duvant, Magali Fillat, Florentine Garaix, et al.
European Journal of Medical Genetics|November 28, 2017
Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel diseaseJoão Farela Neves, Isabel Afonso, Luis Borrego, et al.
Annales De Pathologie|February 14, 2012
[Vasoactive intestinal polypeptide-secreting diffuse ganglioneuromatosis affecting the small intestine and the colon in an infant: an exceptional inaugural manifestation of NF1]Malik Kadri, Alexandre Fabre, Carole Coze, et al.
Annales De Pathologie|January 4, 2022
[Diagnosis of a rare and severe inflammatory bowel disease in an infant with peri-orificial ulcerations]Alexandre Bardet, Florence Riccardi, Julia Torrents, et al.
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