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Corinne Magdelaine

Showing results (1-10 of 43) with videos related to

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Pediatrics|February 15, 2012
Successful use of bisphosphonate and calcimimetic in neonatal severe primary hyperparathyroidismAlexandra Wilhelm-Bals, Paloma Parvex, Corinne Magdelaine, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
IgG neuropathy: an immunoelectron microscopic studyJean-Michel Vallat, Laurent Magy, Philippe Sindou, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
Autosomal-recessive Charcot-Marie-Tooth diseasesJean-Michel Vallat, Meriem Tazir, Corinne Magdelaine, et al.
Bulletin De L'Academie Nationale De Medecine|September 2, 2009
[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations]Benoît Funalot, Corinne Magdelaine, Franck Sturtz, et al.
Bulletin De L'Academie Nationale De Medecine|August 27, 2005
[Autosomal recessive forms of Charcot-Marie-Tooth disease]Jean-Michel Vallat, Djamel Grid, Corinne Magdelaine, et al.
ERJ Open Research|January 14, 2026
Efficacy of morphine on cough in patients with repeat expansions of <i>RFC1</i> and refractory chronic coughLaurent Guilleminault, Pauline Chazelas, Corinne Magdelaine, et al.
Journal of the Peripheral Nervous System : JPNS|April 28, 2017
A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literatureJustine Lerat, Pascal Cintas, Hélène Beauvais-Dzugan, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Severe Charcot-Marie-Tooth disease type 1E caused by a novel p.Phe84Leufs*24 PMP22 point mutationAnne Vital, Guilhem Sole, Philippe Casenave, et al.
Acta Neuropathologica|February 13, 2007
Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritanceJean-Michel Vallat, Laurent Magy, Emmeline Lagrange, et al.
Journal of the Peripheral Nervous System : JPNS|September 14, 2013
CMT4D (NDRG1 mutation): genotype-phenotype correlationsEmilie Ricard, Stéphane Mathis, Corinne Magdelaine, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Pediatrics|February 15, 2012
Successful use of bisphosphonate and calcimimetic in neonatal severe primary hyperparathyroidismAlexandra Wilhelm-Bals, Paloma Parvex, Corinne Magdelaine, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
IgG neuropathy: an immunoelectron microscopic studyJean-Michel Vallat, Laurent Magy, Philippe Sindou, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
Autosomal-recessive Charcot-Marie-Tooth diseasesJean-Michel Vallat, Meriem Tazir, Corinne Magdelaine, et al.
Bulletin De L'Academie Nationale De Medecine|September 2, 2009
[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations]Benoît Funalot, Corinne Magdelaine, Franck Sturtz, et al.
Bulletin De L'Academie Nationale De Medecine|August 27, 2005
[Autosomal recessive forms of Charcot-Marie-Tooth disease]Jean-Michel Vallat, Djamel Grid, Corinne Magdelaine, et al.
ERJ Open Research|January 14, 2026
Efficacy of morphine on cough in patients with repeat expansions of <i>RFC1</i> and refractory chronic coughLaurent Guilleminault, Pauline Chazelas, Corinne Magdelaine, et al.
Journal of the Peripheral Nervous System : JPNS|April 28, 2017
A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literatureJustine Lerat, Pascal Cintas, Hélène Beauvais-Dzugan, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Severe Charcot-Marie-Tooth disease type 1E caused by a novel p.Phe84Leufs*24 PMP22 point mutationAnne Vital, Guilhem Sole, Philippe Casenave, et al.
Acta Neuropathologica|February 13, 2007
Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritanceJean-Michel Vallat, Laurent Magy, Emmeline Lagrange, et al.
Journal of the Peripheral Nervous System : JPNS|September 14, 2013
CMT4D (NDRG1 mutation): genotype-phenotype correlationsEmilie Ricard, Stéphane Mathis, Corinne Magdelaine, et al.
Pageof 5