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Vincent Procaccio

Showing results (51-60 of 197) with videos related to

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Pathology Oncology Research : POR|August 7, 2025
MtDNA copy number enrichment is associated with poor prognosis and eosinophilic morphology in clear cell renal cell carcinomaSarah Bellal, Cyrielle Rolley, Jeremy Richard, et al.
Journal of Assisted Reproduction and Genetics|November 19, 2013
Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?Marc Ferré, Patrizia Amati-Bonneau, Catherine Morinière, et al.
Experimental Neurology|September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutationsJulien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Molecular Genetics and Metabolism|February 3, 2009
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative diseasePrasanth Potluri, Antonio Davila, Eduardo Ruiz-Pesini, et al.
Human Molecular Genetics|December 24, 2004
Friedreich ataxia: the oxidative stress paradoxHervé Seznec, Delphine Simon, Cécile Bouton, et al.
Human Mutation|September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical dataMarc Ferré, Angélique Caignard, Dan Milea, et al.
Brain and Behavior|April 18, 2017
High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosisKornélia Tripolszki, Dóra Török, David Goudenège, et al.
Journal of Hypertension|October 12, 2010
Heme oxygenase-1 induction restores high-blood-flow-dependent remodeling and endothelial function in mesenteric arteries of old ratsMohamed Lamine Freidja, Emilie Vessieres, Nicolas Clere, et al.
Medecine Sciences : M/S|November 13, 2018
[Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS]Aurélien Perrin, Philippe Latour, Vincent Procaccio, et al.
Pageof 20

Showing results (51-60 of 197) with videos related to

Sort By:
Pageof 20
Pathology Oncology Research : POR|August 7, 2025
MtDNA copy number enrichment is associated with poor prognosis and eosinophilic morphology in clear cell renal cell carcinomaSarah Bellal, Cyrielle Rolley, Jeremy Richard, et al.
Journal of Assisted Reproduction and Genetics|November 19, 2013
Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?Marc Ferré, Patrizia Amati-Bonneau, Catherine Morinière, et al.
Experimental Neurology|September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutationsJulien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Molecular Genetics and Metabolism|February 3, 2009
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative diseasePrasanth Potluri, Antonio Davila, Eduardo Ruiz-Pesini, et al.
Human Molecular Genetics|December 24, 2004
Friedreich ataxia: the oxidative stress paradoxHervé Seznec, Delphine Simon, Cécile Bouton, et al.
Human Mutation|September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical dataMarc Ferré, Angélique Caignard, Dan Milea, et al.
Brain and Behavior|April 18, 2017
High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosisKornélia Tripolszki, Dóra Török, David Goudenège, et al.
Journal of Hypertension|October 12, 2010
Heme oxygenase-1 induction restores high-blood-flow-dependent remodeling and endothelial function in mesenteric arteries of old ratsMohamed Lamine Freidja, Emilie Vessieres, Nicolas Clere, et al.
Medecine Sciences : M/S|November 13, 2018
[Towards an harmonization of diagnosis by NGS of neuromuscular diseases - Actions of the Molecular Genetics sub-group of FILNEMUS]Aurélien Perrin, Philippe Latour, Vincent Procaccio, et al.
Pageof 20