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Dominique Bonneau

Showing results (11-20 of 253) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
A phase II, open-label evaluation of cysteamine tolerability in patients with Huntington's diseaseAdriana Prundean, Katia Youssov, Sandrine Humbert, et al.
Medicine and Science in Sports and Exercise|October 9, 2002
Decrease in serum leptin after prolonged physical activity in menDanielle Gomez-Merino, Mounir Chennaoui, Catherine Drogou, et al.
Ergonomics|November 9, 2006
External and internal geometry of European adultsSamuel Bertrand, Wafa Skalli, Laurent Delacherie, et al.
American Journal of Medical Genetics. Part A|October 16, 2004
Absence of deletion at the SOX2 locus in a case of microphthalmia and esophageal atresiaDominique Bonneau, Agnès Guichet, Françoise Boussion, et al.
Frontiers in Physiology|December 5, 2015
Salivary Hormones Response to Preparation and Pre-competitive Training of World-class Level AthletesGaël Guilhem, Christine Hanon, Nicolas Gendreau, et al.
JMIR Mental Health|September 15, 2021
Mobile App for Parental Empowerment for Caregivers of Children With Autism Spectrum Disorders: Prospective Open TrialOlivier Bonnot, Vladimir Adrien, Veronique Venelle, et al.
Archives of Dermatology|September 13, 2002
Pitfalls in clinical diagnosis of female carriers of X-linked hypohidrotic ectodermal dysplasiaMarie-Claire Vincent, Mireille Cossée, Pierre Vabres, et al.
American Journal of Ophthalmology|March 5, 2003
Retinal angioma in a patient with Cowden diseaseJean-Jacques Gicquel, Pierre Vabres, Dominique Bonneau, et al.
World Journal of Gastroenterology|November 1, 2012
A de novo germline MLH1 mutation in a Lynch syndrome patient with discordant immunohistochemical and molecular biology test resultsFabrice Airaud, Sébastien Küry, Isabelle Valo, et al.
Orphanet Journal of Rare Diseases|December 28, 2011
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2KJulien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Pageof 26

Showing results (11-20 of 253) with videos related to

Sort By:
Pageof 26
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
A phase II, open-label evaluation of cysteamine tolerability in patients with Huntington's diseaseAdriana Prundean, Katia Youssov, Sandrine Humbert, et al.
Medicine and Science in Sports and Exercise|October 9, 2002
Decrease in serum leptin after prolonged physical activity in menDanielle Gomez-Merino, Mounir Chennaoui, Catherine Drogou, et al.
Ergonomics|November 9, 2006
External and internal geometry of European adultsSamuel Bertrand, Wafa Skalli, Laurent Delacherie, et al.
American Journal of Medical Genetics. Part A|October 16, 2004
Absence of deletion at the SOX2 locus in a case of microphthalmia and esophageal atresiaDominique Bonneau, Agnès Guichet, Françoise Boussion, et al.
Frontiers in Physiology|December 5, 2015
Salivary Hormones Response to Preparation and Pre-competitive Training of World-class Level AthletesGaël Guilhem, Christine Hanon, Nicolas Gendreau, et al.
JMIR Mental Health|September 15, 2021
Mobile App for Parental Empowerment for Caregivers of Children With Autism Spectrum Disorders: Prospective Open TrialOlivier Bonnot, Vladimir Adrien, Veronique Venelle, et al.
Archives of Dermatology|September 13, 2002
Pitfalls in clinical diagnosis of female carriers of X-linked hypohidrotic ectodermal dysplasiaMarie-Claire Vincent, Mireille Cossée, Pierre Vabres, et al.
American Journal of Ophthalmology|March 5, 2003
Retinal angioma in a patient with Cowden diseaseJean-Jacques Gicquel, Pierre Vabres, Dominique Bonneau, et al.
World Journal of Gastroenterology|November 1, 2012
A de novo germline MLH1 mutation in a Lynch syndrome patient with discordant immunohistochemical and molecular biology test resultsFabrice Airaud, Sébastien Küry, Isabelle Valo, et al.
Orphanet Journal of Rare Diseases|December 28, 2011
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2KJulien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Pageof 26