Publications by authors named "Djamel Grid"

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Pantothenate kinase-associated neurodegeneration: clinical description of 10 patients and identification of new mutations.
Salima Assami, Hamid Azzedine, Sonia Nouioua, Emeline Mundwiller, Soulaiman Mahoui, Djamel Grid

Mov Disord· August 2011

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Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.
Sonia Nouioua, Tarik Hamadouche, Benoit Funalot, Rafaëlle Bernard, Nora Bellatache, Djamel Grid

Neuromuscul Disord· August 2011

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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
Cyril Goizet, Amir Boukhris, Alexandra Durr, Christian Beetz, Jeremy Truchetto, Djamel Grid

Brain· June 2009

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Phenotypic variability in giant axonal neuropathy.
Meriem Tazir, Sonia Nouioua, Laurent Magy, Kathrin Huehne, Salima Assami, Djamel Grid

Neuromuscul Disord· April 2009

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Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.
Nizar Elleuch, Naima Bouslam, Sylvain Hanein, Alexander Lossos, Abdelmadjid Hamri, Djamel Grid

Neurogenetics· November 2007

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Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
Stephan Klebe, Alexandra Durr, Naima Bouslam, Djamel Grid, Caroline Paternotte

Am J Med Genet B Neuropsychiatr Genet· October 2007

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Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H.
Valérie Delague, Arnaud Jacquier, Tarik Hamadouche, Yannick Poitelon, Cécile Baudot, Djamel Grid

Am J Hum Genet· July 2007

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Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance.
Jean-Michel Vallat, Laurent Magy, Emmeline Lagrange, Franck Sturtz, Corinne Magdelaine, Djamel Grid

Acta Neuropathol· April 2007

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Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
Giovanni Stevanin, Filippo M Santorelli, Hamid Azzedine, Paula Coutinho, Jacques Chomilier, Djamel Grid

Nat Genet· March 2007

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Autosomal-recessive Charcot-Marie-Tooth diseases.
Jean-Michel Vallat, Meriem Tazir, Corinne Magdelaine, Franck Sturtz, Djamel Grid

J Neuropathol Exp Neurol· May 2005

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[Autosomal recessive forms of Charcot-Marie-Tooth disease].
Jean-Michel Vallat, Djamel Grid, Corinne Magdelaine, Franck Sturtz, Nicolas Levy

Bull Acad Natl Med· January 2005

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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations.
Bruno Moulard, Pierre Genton, Djamel Grid, Marc Jeanpierre, Réda Ouazzani

Hum Genet· September 2002

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Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
Annachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, Jean-Michel Vallat, Meriem Tazir, Djamel Grid

Am J Hum Genet· March 2002

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