Search research articles
Contact Us
Filters
Showing results (21-30 of 33) with videos related to
Page
of 4
Sort By:
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 Outcomes
Fanny 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 diabetes
Nawel 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 disease
Yahsou Delmas, Sébastien Helou, Pierre Chabanier, et al.
Acta Neuropathologica
|
December 6, 2008
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases
Laurent 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 microphthalmia
Nicolas Chassaing, Virginie Siani, Dominique Carles, et al.
Plos One
|
January 18, 2013
Reduced placental telomere length during pregnancies complicated by intrauterine growth restriction
Jérôme 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 diagnosis
Francois 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 lissencephaly
Sandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Journal of Medical Genetics
|
May 12, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complex
Nicolas 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 RBM8A
Simon Boussion, Fabienne Escande, Anne-Sophie Jourdain, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 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 Outcomes
Fanny 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 diabetes
Nawel 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 disease
Yahsou Delmas, Sébastien Helou, Pierre Chabanier, et al.
Acta Neuropathologica
|
December 6, 2008
Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases
Laurent 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 microphthalmia
Nicolas Chassaing, Virginie Siani, Dominique Carles, et al.
Plos One
|
January 18, 2013
Reduced placental telomere length during pregnancies complicated by intrauterine growth restriction
Jérôme 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 diagnosis
Francois 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 lissencephaly
Sandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Journal of Medical Genetics
|
May 12, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complex
Nicolas 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 RBM8A
Simon Boussion, Fabienne Escande, Anne-Sophie Jourdain, et al.
Page
of 4