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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 disease
Adriana 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 men
Danielle Gomez-Merino, Mounir Chennaoui, Catherine Drogou, et al.
Ergonomics
|
November 9, 2006
External and internal geometry of European adults
Samuel 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 atresia
Dominique 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 Athletes
Gaël 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 Trial
Olivier 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 dysplasia
Marie-Claire Vincent, Mireille Cossée, Pierre Vabres, et al.
American Journal of Ophthalmology
|
March 5, 2003
Retinal angioma in a patient with Cowden disease
Jean-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 results
Fabrice 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 2K
Julien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Page
of 26
Search research articles
Search
Showing results (11-20 of 253) with videos related to
Sort By:
Page
of 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 disease
Adriana 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 men
Danielle Gomez-Merino, Mounir Chennaoui, Catherine Drogou, et al.
Ergonomics
|
November 9, 2006
External and internal geometry of European adults
Samuel 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 atresia
Dominique 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 Athletes
Gaël 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 Trial
Olivier 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 dysplasia
Marie-Claire Vincent, Mireille Cossée, Pierre Vabres, et al.
American Journal of Ophthalmology
|
March 5, 2003
Retinal angioma in a patient with Cowden disease
Jean-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 results
Fabrice 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 2K
Julien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Page
of 26