Publications by authors named "Frederic Dubas"

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Compound heterozygous mutations of the TNXB gene cause primary myopathy.
Isabelle Pénisson-Besnier, Valérie Allamand, Philippe Beurrier, Ludovic Martin, Joost Schalkwijk, Frédéric Dubas

Neuromuscul Disord· August 2013

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Myopathy caused by anoctamin 5 mutations and necrotizing vasculitis.
Isabelle Pénisson-Besnier, Jean-Paul Saint-André, Debbie Hicks, Anna Sarkozy, Anne Croué, Frédéric Dubas

J Neurol· September 2012

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Axon cytoskeleton ultrastructure in chronic inflammatory demyelinating polyneuropathy.
Catherine Fressinaud, Frédéric Dubas

Muscle Nerve· September 2011

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The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's disease.
Philippe Allain, Véronique Gaura, Luciano Fasotti, Valérie Chauviré, Adriana Prundean, Frédéric Dubas

Neuropsychologia· July 2011

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Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.
Christophe Verny, Naig Guegen, Valerie Desquiret, Arnaud Chevrollier, Adriana Prundean, Frederic Dubas

Mitochondrion· January 2011

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Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, Valérie Desquiret, Christophe Verny, Frédéric Dubas

Exp Neurol· January 2011

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Leukodystrophies: clinical and therapeutic aspects.
Franck Letournel, Frédéric Dubas

Handb Clin Neurol· December 2010

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Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy.
Cédric Lamirel, Julien Cassereau, Isabelle Cochereau, Catherine Vignal-Clermont, Olivier Pajot, Frédéric Dubas

J Neurol Neurosurg Psychiatry· May 2010

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[Multiple sclerosis].
Clarisse Scherer, Frédéric Dubas

Rev Prat· May 2009

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Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, Marie-Claire Malinge, Franck Letournel, Frédéric Dubas

Neurogenetics· April 2009

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Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.
Julien Cassereau, Christian Lavigne, Franck Letournel, Alaa Ghali, Christophe Verny, Frédéric Dubas

J Peripher Nerv Syst· September 2008

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Script representation in patients with Alzheimer's disease.
Philippe Allain, Didier Le Gall, Céline Foucher, Frédérique Etcharry-Bouyx, Jean Barré, Frédéric Dubas

Cortex· March 2008

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[Executive functioning and normal aging: a study of arithmetic word-problem-solving].
Philippe Allain, Mélina Kauffmann, Frédéric Dubas, Gilles Berrut, Didier Le Gall

Psychol Neuropsychiatr Vieil· December 2007

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Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.
Brigitte Ricard-Mousnier, Sylvie N'Guyen, Frédéric Dubas, François Pouplard, Agnès Guichet

Epileptic Disord· September 2007

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Executive functions in normal aging: an examination of script sequencing, script sorting, and script monitoring.
Philippe Allain, Gilles Berrut, Frédérique Etcharry-Bouyx, Jean Barré, Frédéric Dubas

J Gerontol B Psychol Sci Soc Sci· May 2007

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A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
Isabelle Pénisson-Besnier, Nicole Monnier, Annick Toutain, Frédéric Dubas, Nigel Laing

Neuromuscul Disord· April 2007

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Diagnosis of myotubular myopathy in the oldest known manifesting female carrier: a clinical and genetic study.
Isabelle Pénisson-Besnier, Valérie Biancalana, Pascal Reynier, Mireille Cossée, Frédéric Dubas

Neuromuscul Disord· February 2007

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[Nontraumatic coma].
Frédéric Dubas

Rev Prat· February 2007

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Refsum's disease may mimic familial Guillain Barre syndrome.
Christophe Verny, Adriana Prundean, Guillaume Nicolas, Vivien Pautot, Dominique Maugin, Frederic Dubas

Neuromuscul Disord· November 2006

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Myotilinopathy in a family with late onset myopathy.
Isabelle Pénisson-Besnier, Kati Talvinen, Catherine Dumez, Anna Vihola, Frédéric Dubas

Neuromuscul Disord· July 2006

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
Anne Rovelet-Lecrux, Didier Hannequin, Gregory Raux, Nathalie Le Meur, Annie Laquerrière, Frédéric Dubas

Nat Genet· January 2006

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Isolated Horner's syndrome may herald stroke.
Jean-Michel de Bray, Ralf Baumgartner, Benoit Guillon, Vivien Pautot, Rainer Dziewas, Frédéric Dubas

Cerebrovasc Dis· June 2005

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[Cerebral microangiopathies].
Guillaume Marc, Frédéric Dubas

Psychol Neuropsychiatr Vieil· June 2005

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Monitoring processes and metamemory experience in patients with dysexecutive syndrome.
Karine Pinon, Phillipe Allain, Mohamed Zied Kefi, Frédéric Dubas, Didier Le Gall

Brain Cogn· March 2005

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Executive functioning in normal aging: a study of action planning using the Zoo Map Test.
Philippe Allain, Sylvie Nicoleau, Karine Pinon, Frédérique Etcharry-Bouyx, Jean Barré, Frédéric Dubas

Brain Cogn· February 2005

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