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Dominique Bonneau

Showing results (21-30 of 253) with videos related to

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Journal of Magnetic Resonance Imaging : JMRI|October 27, 2009
Comparison of methods to assess quadriceps muscle volume using magnetic resonance imagingAntoine Nordez, Erwan Jolivet, Ingrid Südhoff, et al.
Clinical Dysmorphology|May 27, 2014
Extensive Mongolian spots in 4p16.3 deletion (Wolf-Hirschhorn syndrome)Alban Ziegler, Agnès Guichet, Lucille Pinson, et al.
European Journal of Applied Physiology|August 5, 2004
Leptin, catecholamines and free fatty acids related to reduced recovery delays after trainingFrançois Denis Desgorces, Mounir Chennaoui, Danielle Gomez-Merino, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
Macrocephaly-cutis marmorata telangiectatica congenita: seven cases including two with unusual cerebral manifestationsFabienne Giuliano, Albert David, Patrick Edery, et al.
Brain and Cognition|January 5, 2005
Arithmetic word-problem-solving in Huntington's diseasePhilippe Allain, Christophe Verny, Ghislaine Aubin, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
The British Journal of Ophthalmology|August 3, 2010
Never too old to harbour a young man's disease?Sylvia Giraudet, Cédric Lamirel, Patrizia Amati-Bonneau, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2018
A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature ReviewLucie Pépin, Estelle Colin, Marine Tessarech, et al.
Pediatric Research|September 17, 2004
Effect of single and multiple courses of prenatal corticosteroids on 17-hydroxyprogesterone levels: implication for neonatal screening of congenital adrenal hyperplasiaFrédérique Gatelais, Jacques Berthelot, Frédérique Beringue, et al.
Neuromuscular Disorders : NMD|August 29, 2006
Refsum's disease may mimic familial Guillain Barre syndromeChristophe Verny, Adriana Prundean, Guillaume Nicolas, et al.
Pageof 26

Showing results (21-30 of 253) with videos related to

Sort By:
Pageof 26
Journal of Magnetic Resonance Imaging : JMRI|October 27, 2009
Comparison of methods to assess quadriceps muscle volume using magnetic resonance imagingAntoine Nordez, Erwan Jolivet, Ingrid Südhoff, et al.
Clinical Dysmorphology|May 27, 2014
Extensive Mongolian spots in 4p16.3 deletion (Wolf-Hirschhorn syndrome)Alban Ziegler, Agnès Guichet, Lucille Pinson, et al.
European Journal of Applied Physiology|August 5, 2004
Leptin, catecholamines and free fatty acids related to reduced recovery delays after trainingFrançois Denis Desgorces, Mounir Chennaoui, Danielle Gomez-Merino, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
Macrocephaly-cutis marmorata telangiectatica congenita: seven cases including two with unusual cerebral manifestationsFabienne Giuliano, Albert David, Patrick Edery, et al.
Brain and Cognition|January 5, 2005
Arithmetic word-problem-solving in Huntington's diseasePhilippe Allain, Christophe Verny, Ghislaine Aubin, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
The British Journal of Ophthalmology|August 3, 2010
Never too old to harbour a young man's disease?Sylvia Giraudet, Cédric Lamirel, Patrizia Amati-Bonneau, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2018
A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature ReviewLucie Pépin, Estelle Colin, Marine Tessarech, et al.
Pediatric Research|September 17, 2004
Effect of single and multiple courses of prenatal corticosteroids on 17-hydroxyprogesterone levels: implication for neonatal screening of congenital adrenal hyperplasiaFrédérique Gatelais, Jacques Berthelot, Frédérique Beringue, et al.
Neuromuscular Disorders : NMD|August 29, 2006
Refsum's disease may mimic familial Guillain Barre syndromeChristophe Verny, Adriana Prundean, Guillaume Nicolas, et al.
Pageof 26