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Dominique Bonneau

Showing results (71-80 of 253) with videos related to

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Journal of Huntington'S Disease|February 20, 2025
Social cognition profile in early Huntington disease: Insight from neuropsychological assessment and structural neuroimagingMarie Caillaud, Mickael Laisney, Alexandre Bejanin, et al.
Annals of Neurology|March 14, 2002
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findingsDominique Bonneau, Annick Toutain, Annie Laquerrière, et al.
Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Human Genetics|July 27, 2021
ZNF668 deficiency causes a recognizable disorder of DNA damage repairHessa S Alsaif, Hatoon Al Ali, Eissa Faqeih, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
International Journal of Cancer|June 29, 2004
Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumorsKarmen Stankov, Alessandro Pastore, Luca Toschi, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Pageof 26

Showing results (71-80 of 253) with videos related to

Sort By:
Pageof 26
Journal of Huntington'S Disease|February 20, 2025
Social cognition profile in early Huntington disease: Insight from neuropsychological assessment and structural neuroimagingMarie Caillaud, Mickael Laisney, Alexandre Bejanin, et al.
Annals of Neurology|March 14, 2002
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findingsDominique Bonneau, Annick Toutain, Annie Laquerrière, et al.
Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Human Genetics|July 27, 2021
ZNF668 deficiency causes a recognizable disorder of DNA damage repairHessa S Alsaif, Hatoon Al Ali, Eissa Faqeih, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
International Journal of Cancer|June 29, 2004
Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumorsKarmen Stankov, Alessandro Pastore, Luca Toschi, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Pageof 26