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Dominique Carles

Showing results (21-30 of 33) with videos related to

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The American Journal of Surgical Pathology|August 11, 2020
Chronic Intervillositis of Unknown Etiology: Development of a Grading and Scoring System That Is Strongly Associated With Poor Perinatal OutcomesFanny Sauvestre, Aurélien Mattuizzi, Loïc Sentilhes, et al.
Journal of Ethnopharmacology|May 30, 2015
Effect of Centaurium erythraea Rafn, Artemisia herba-alba Asso and Trigonella foenum-graecum L. on liver fat accumulation in C57BL/6J mice with high-fat diet-induced type 2 diabetesNawel Hamza, Bénédicte Berke, Catherine Cheze, et al.
BMC Pregnancy and Childbirth|June 18, 2015
Incidence of obstetrical thrombotic thrombocytopenic purpura in a retrospective study within thrombocytopenic pregnant women. A difficult diagnosis and a treatable diseaseYahsou Delmas, Sébastien Helou, Pierre Chabanier, et al.
Acta Neuropathologica|December 6, 2008
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal casesLaurent Pasquier, Pascale Marcorelles, Philippe Loget, et al.
American Journal of Medical Genetics. Part A|July 8, 2005
X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaNicolas Chassaing, Virginie Siani, Dominique Carles, et al.
Plos One|January 18, 2013
Reduced placental telomere length during pregnancies complicated by intrauterine growth restrictionJérôme Toutain, Martina Prochazkova-Carlotti, David Cappellen, et al.
Human Reproduction (Oxford, England)|August 16, 2011
Contribution of referent pathologists to the quality of trophoblastic diseases diagnosisFrancois Golfier, Jessica Clerc, Touria Hajri, et al.
American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Journal of Medical Genetics|May 12, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complexNicolas Chassaing, Susanna Sorrentino, Erica E Davis, et al.
Human Mutation|April 1, 2020
TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8ASimon Boussion, Fabienne Escande, Anne-Sophie Jourdain, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
The American Journal of Surgical Pathology|August 11, 2020
Chronic Intervillositis of Unknown Etiology: Development of a Grading and Scoring System That Is Strongly Associated With Poor Perinatal OutcomesFanny Sauvestre, Aurélien Mattuizzi, Loïc Sentilhes, et al.
Journal of Ethnopharmacology|May 30, 2015
Effect of Centaurium erythraea Rafn, Artemisia herba-alba Asso and Trigonella foenum-graecum L. on liver fat accumulation in C57BL/6J mice with high-fat diet-induced type 2 diabetesNawel Hamza, Bénédicte Berke, Catherine Cheze, et al.
BMC Pregnancy and Childbirth|June 18, 2015
Incidence of obstetrical thrombotic thrombocytopenic purpura in a retrospective study within thrombocytopenic pregnant women. A difficult diagnosis and a treatable diseaseYahsou Delmas, Sébastien Helou, Pierre Chabanier, et al.
Acta Neuropathologica|December 6, 2008
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal casesLaurent Pasquier, Pascale Marcorelles, Philippe Loget, et al.
American Journal of Medical Genetics. Part A|July 8, 2005
X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmiaNicolas Chassaing, Virginie Siani, Dominique Carles, et al.
Plos One|January 18, 2013
Reduced placental telomere length during pregnancies complicated by intrauterine growth restrictionJérôme Toutain, Martina Prochazkova-Carlotti, David Cappellen, et al.
Human Reproduction (Oxford, England)|August 16, 2011
Contribution of referent pathologists to the quality of trophoblastic diseases diagnosisFrancois Golfier, Jessica Clerc, Touria Hajri, et al.
American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Journal of Medical Genetics|May 12, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complexNicolas Chassaing, Susanna Sorrentino, Erica E Davis, et al.
Human Mutation|April 1, 2020
TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8ASimon Boussion, Fabienne Escande, Anne-Sophie Jourdain, et al.
Pageof 4