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Olivier Faivre

Showing results (1-10 of 18) with videos related to

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Plos One|May 15, 2008
Visual coding in locust photoreceptorsOlivier Faivre, Mikko Juusola
JAMA Dermatology|November 22, 2013
Juvenile xanthogranuloma and nevus anemicus in the diagnosis of neurofibromatosis type 1Faustine Ferrari, Alice Masurel, Laurence Olivier-Faivre, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 11, 2011
[A new prenatal diagnosis case of frontonasal dysplasia]V Guigue, A Martin, M Mangin, et al.
Nature Neuroscience|March 6, 2012
Tonic signaling from O₂ sensors sets neural circuit activity and behavioral stateKarl Emanuel Busch, Patrick Laurent, Zoltan Soltesz, et al.
Journal of Clinical Medicine|April 28, 2023
Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of AgeJean Sénémaud, Marine Gaudry, Elisabeth Jouve, et al.
Archives of Cardiovascular Diseases|July 13, 2010
Rationale and design of a randomized clinical trial (Marfan Sartan) of angiotensin II receptor blocker therapy versus placebo in individuals with Marfan syndromeDelphine Detaint, Philippe Aegerter, Florence Tubach, et al.
Familial Cancer|September 27, 2013
Diversity of the clinical presentation of the MMR gene biallelic mutationsGaëlle Bougeard, Laurence Olivier-Faivre, Stéphanie Baert-Desurmont, et al.
Investigative Ophthalmology & Visual Science|September 11, 2020
Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic FactorsVincent Lhussiez, Elisabeth Dubus, Quénol Cesar, et al.
JAMA|June 7, 2011
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndromeValérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, et al.
Journal of Medical Genetics|November 21, 2014
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlationCyril Mignot, Laetitia Lambert, Laurent Pasquier, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Plos One|May 15, 2008
Visual coding in locust photoreceptorsOlivier Faivre, Mikko Juusola
JAMA Dermatology|November 22, 2013
Juvenile xanthogranuloma and nevus anemicus in the diagnosis of neurofibromatosis type 1Faustine Ferrari, Alice Masurel, Laurence Olivier-Faivre, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 11, 2011
[A new prenatal diagnosis case of frontonasal dysplasia]V Guigue, A Martin, M Mangin, et al.
Nature Neuroscience|March 6, 2012
Tonic signaling from O₂ sensors sets neural circuit activity and behavioral stateKarl Emanuel Busch, Patrick Laurent, Zoltan Soltesz, et al.
Journal of Clinical Medicine|April 28, 2023
Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of AgeJean Sénémaud, Marine Gaudry, Elisabeth Jouve, et al.
Archives of Cardiovascular Diseases|July 13, 2010
Rationale and design of a randomized clinical trial (Marfan Sartan) of angiotensin II receptor blocker therapy versus placebo in individuals with Marfan syndromeDelphine Detaint, Philippe Aegerter, Florence Tubach, et al.
Familial Cancer|September 27, 2013
Diversity of the clinical presentation of the MMR gene biallelic mutationsGaëlle Bougeard, Laurence Olivier-Faivre, Stéphanie Baert-Desurmont, et al.
Investigative Ophthalmology & Visual Science|September 11, 2020
Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic FactorsVincent Lhussiez, Elisabeth Dubus, Quénol Cesar, et al.
JAMA|June 7, 2011
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndromeValérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, et al.
Journal of Medical Genetics|November 21, 2014
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlationCyril Mignot, Laetitia Lambert, Laurent Pasquier, et al.
Pageof 2