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Alexandra Benachi

Showing results (221-230 of 324) with videos related to

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Clinical Genetics|October 23, 2022
Management of copy number variants associated with incomplete penetrance and variable expressivity-Results of a French surveyFloriane Lejamtel, Cécile Oheix, Elisa Morales, et al.
Prenatal Diagnosis|October 11, 2019
Variability in antenatal prognostication of fetal diaphragmatic hernia across the North American Fetal Therapy Network (NAFTNet)Nimrah Abbasi, Magda Sanz Cortes, Rodrigo Ruano, et al.
Prenatal Diagnosis|May 28, 2004
A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmentiJulie Steffann, Valérie Raclin, Asmae Smahi, et al.
Trials|February 24, 2021
Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic herniaSimen Vergote, Felix De Bie, Jan Bosteels, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 6, 2015
Increased TGF-β: a drawback of tracheal occlusion in human and experimental congenital diaphragmatic hernia?Aline Vuckovic, Susanne Herber-Jonat, Andreas W Flemmer, et al.
Orphanet Journal of Rare Diseases|September 6, 2013
FGF10 Signaling differences between type I pleuropulmonary blastoma and congenital cystic adenomatoid malformationGuillaume Lezmi, Virginie Verkarre, Naziha Khen-Dunlop, et al.
Journal of Pediatric Surgery|January 18, 2011
Technical aspects of fetal endoscopic tracheal occlusion for congenital diaphragmatic herniaJan Deprest, Kypros Nicolaides, Elisa Done', et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
American Journal of Obstetrics and Gynecology|June 14, 2021
Chronic histiocytic intervillositis: manifestation of placental alloantibody-mediated rejectionAlexandra Benachi, Marion Rabant, Jelena Martinovic, et al.
Plos One|September 12, 2008
Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung developmentAlice Hadchouel, Fabrice Decobert, Marie-Laure Franco-Montoya, et al.
Pageof 33

Showing results (221-230 of 324) with videos related to

Sort By:
Pageof 33
Clinical Genetics|October 23, 2022
Management of copy number variants associated with incomplete penetrance and variable expressivity-Results of a French surveyFloriane Lejamtel, Cécile Oheix, Elisa Morales, et al.
Prenatal Diagnosis|October 11, 2019
Variability in antenatal prognostication of fetal diaphragmatic hernia across the North American Fetal Therapy Network (NAFTNet)Nimrah Abbasi, Magda Sanz Cortes, Rodrigo Ruano, et al.
Prenatal Diagnosis|May 28, 2004
A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmentiJulie Steffann, Valérie Raclin, Asmae Smahi, et al.
Trials|February 24, 2021
Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic herniaSimen Vergote, Felix De Bie, Jan Bosteels, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 6, 2015
Increased TGF-β: a drawback of tracheal occlusion in human and experimental congenital diaphragmatic hernia?Aline Vuckovic, Susanne Herber-Jonat, Andreas W Flemmer, et al.
Orphanet Journal of Rare Diseases|September 6, 2013
FGF10 Signaling differences between type I pleuropulmonary blastoma and congenital cystic adenomatoid malformationGuillaume Lezmi, Virginie Verkarre, Naziha Khen-Dunlop, et al.
Journal of Pediatric Surgery|January 18, 2011
Technical aspects of fetal endoscopic tracheal occlusion for congenital diaphragmatic herniaJan Deprest, Kypros Nicolaides, Elisa Done', et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
American Journal of Obstetrics and Gynecology|June 14, 2021
Chronic histiocytic intervillositis: manifestation of placental alloantibody-mediated rejectionAlexandra Benachi, Marion Rabant, Jelena Martinovic, et al.
Plos One|September 12, 2008
Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung developmentAlice Hadchouel, Fabrice Decobert, Marie-Laure Franco-Montoya, et al.
Pageof 33