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Dominique Bonneau

Showing results (41-50 of 253) with videos related to

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Archives of Dermatology|March 19, 2008
Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXELudovic Martin, Frédéric Maître, Pierre Bonicel, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndromeIsabelle Pénisson-Besnier, Thibaud Lebouvier, Marie-Pierre Moizard, et al.
Prenatal Diagnosis|April 21, 2012
Prenatal diagnosis of CHARGE syndrome by identification of a novel CHD7 mutation in a previously unaffected familyEstelle Colin, Dominique Bonneau, Francoise Boussion, et al.
Ultrasound in Medicine & Biology|July 2, 2015
Reliable protocol for shear wave elastography of lower limb muscles at rest and during passive stretchingGuillaume Dubois, Walid Kheireddine, Claudio Vergari, et al.
BMC Research Notes|October 25, 2013
Is ABCC6 a genuine mitochondrial protein?Marc Ferré, Pascal Reynier, Arnaud Chevrollier, et al.
Annales De Pathologie|September 23, 2017
[An atypical case of lipoid proteinosis]Xavier Grimaux, Rida El Ayoubi, Magalie Rabin, et al.
Neuropsychologia|July 18, 2017
Dissociation between decision-making under risk and decision-making under ambiguity in premanifest and manifest Huntington's diseaseNajia Adjeroud, Jeremy Besnard, Christophe Verny, et al.
Diseases of the Colon and Rectum|August 4, 2007
Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristicsGuillaume Bouguen, Sylvain Manfredi, Martine Blayau, et al.
Social Cognitive and Affective Neuroscience|July 27, 2015
Theory of mind and empathy in preclinical and clinical Huntington's diseaseNajia Adjeroud, Jérémy Besnard, Nicole El Massioui, et al.
Clinical Genetics|July 11, 2019
Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disabilityAlban Ziegler, Patricia Bader, Kirsty McWalter, et al.
Pageof 26

Showing results (41-50 of 253) with videos related to

Sort By:
Pageof 26
Archives of Dermatology|March 19, 2008
Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXELudovic Martin, Frédéric Maître, Pierre Bonicel, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndromeIsabelle Pénisson-Besnier, Thibaud Lebouvier, Marie-Pierre Moizard, et al.
Prenatal Diagnosis|April 21, 2012
Prenatal diagnosis of CHARGE syndrome by identification of a novel CHD7 mutation in a previously unaffected familyEstelle Colin, Dominique Bonneau, Francoise Boussion, et al.
Ultrasound in Medicine & Biology|July 2, 2015
Reliable protocol for shear wave elastography of lower limb muscles at rest and during passive stretchingGuillaume Dubois, Walid Kheireddine, Claudio Vergari, et al.
BMC Research Notes|October 25, 2013
Is ABCC6 a genuine mitochondrial protein?Marc Ferré, Pascal Reynier, Arnaud Chevrollier, et al.
Annales De Pathologie|September 23, 2017
[An atypical case of lipoid proteinosis]Xavier Grimaux, Rida El Ayoubi, Magalie Rabin, et al.
Neuropsychologia|July 18, 2017
Dissociation between decision-making under risk and decision-making under ambiguity in premanifest and manifest Huntington's diseaseNajia Adjeroud, Jeremy Besnard, Christophe Verny, et al.
Diseases of the Colon and Rectum|August 4, 2007
Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristicsGuillaume Bouguen, Sylvain Manfredi, Martine Blayau, et al.
Social Cognitive and Affective Neuroscience|July 27, 2015
Theory of mind and empathy in preclinical and clinical Huntington's diseaseNajia Adjeroud, Jérémy Besnard, Nicole El Massioui, et al.
Clinical Genetics|July 11, 2019
Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disabilityAlban Ziegler, Patricia Bader, Kirsty McWalter, et al.
Pageof 26