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Claude Bendavid

Showing results (41-50 of 69) with videos related to

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Human Mutation|January 30, 2009
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanismErich Roessler, Felicitas Lacbawan, Christèle Dubourg, et al.
World Journal of Urology|November 20, 2019
Urinary biomarkers profiles in patients with neurogenic detrusor overactivity according to their neurological conditionClaire Richard, Claude Bendavid, Juliette Hascoet, et al.
Scientific Reports|September 24, 2021
Accuracy of citrulline, I-FABP and D-lactate in the diagnosis of acute mesenteric ischemiaAlexandre Nuzzo, Kevin Guedj, Sonja Curac, 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.
Human Genetics|December 3, 2005
Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genesClaude Bendavid, Christèle Dubourg, Isabelle Gicquel, et al.
Orphanet Journal of Rare Diseases|March 17, 2011
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like lociKarine Morcel, Tanguy Watrin, Laurent Pasquier, et al.
Human Molecular Genetics|January 4, 2011
NOTCH, a new signaling pathway implicated in holoprosencephalyValérie Dupé, Lucie Rochard, Sandra Mercier, et al.
American Journal of Medical Genetics. Part A|June 17, 2009
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletionEilis A Boudreau, Kyle P Johnson, Angela R Jackman, et al.
Molecular Endocrinology (Baltimore, Md.)|May 14, 2005
Haploinsufficiency of cytochrome P450 17alpha-hydroxylase/17,20 lyase (CYP17) causes infertility in male miceYing Liu, Zhi-Xing Yao, Claude Bendavid, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 4, 2013
Caesarean section at term: the relationship between neonatal respiratory morbidity and microviscosity in amniotic fluidVincent Lavoué, Laure Voguet, Bruno Laviolle, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Human Mutation|January 30, 2009
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanismErich Roessler, Felicitas Lacbawan, Christèle Dubourg, et al.
World Journal of Urology|November 20, 2019
Urinary biomarkers profiles in patients with neurogenic detrusor overactivity according to their neurological conditionClaire Richard, Claude Bendavid, Juliette Hascoet, et al.
Scientific Reports|September 24, 2021
Accuracy of citrulline, I-FABP and D-lactate in the diagnosis of acute mesenteric ischemiaAlexandre Nuzzo, Kevin Guedj, Sonja Curac, 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.
Human Genetics|December 3, 2005
Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genesClaude Bendavid, Christèle Dubourg, Isabelle Gicquel, et al.
Orphanet Journal of Rare Diseases|March 17, 2011
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like lociKarine Morcel, Tanguy Watrin, Laurent Pasquier, et al.
Human Molecular Genetics|January 4, 2011
NOTCH, a new signaling pathway implicated in holoprosencephalyValérie Dupé, Lucie Rochard, Sandra Mercier, et al.
American Journal of Medical Genetics. Part A|June 17, 2009
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletionEilis A Boudreau, Kyle P Johnson, Angela R Jackman, et al.
Molecular Endocrinology (Baltimore, Md.)|May 14, 2005
Haploinsufficiency of cytochrome P450 17alpha-hydroxylase/17,20 lyase (CYP17) causes infertility in male miceYing Liu, Zhi-Xing Yao, Claude Bendavid, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 4, 2013
Caesarean section at term: the relationship between neonatal respiratory morbidity and microviscosity in amniotic fluidVincent Lavoué, Laure Voguet, Bruno Laviolle, et al.
Pageof 7