MOUVEMENTS ANORMAUX = Movement disordersBEREAU, Matthieu; TRANCHANT, Christine.La Revue du praticien (Paris). 2014, Vol 64, Num 4, pp 561-568, issn 0035-2640, 8 p.Article

Ataxies cérébelleuses autosomiques recessives = Autosomal recessive cerebellar ataxiasTRANCHANT, Christine; ANHEIM, Mathieu.La Presse médicale (1983). 2009, Vol 38, Num 12, pp 1852-1859, issn 0755-4982, 8 p.Article

Mononeuropathies infectieuses : Neuropathies périphériques = INFECTIOUS MONONEUROPATHIES TOXIC NEUROPATHIES ASSOCIATED WITH INDUSTRIAL AGENTSMARCEL, Christophe; TRANCHANT, Christine.La Revue du praticien (Paris). 2008, Vol 58, Num 17, pp 1900-1902, issn 0035-2640, 3 p.Article

Neuroborréliose : quand y penser ?BLANC, Frédéric; TRANCHANT, Christine.La Revue du praticien. Médecine générale. 2007, Num 782-783, pp 843-846, issn 0989-2737, 4 p.Article

Q263: MYASTHÉNIE = MyastheniaFLEURY-LESAUNIER, Marie-Céline; TRANCHANT, Christine.La Revue du praticien (Paris). 2013, Vol 63, Num 1, pp 109-112, issn 0035-2640, 4 p.Article

The Autosomal Recessive Cerebellar AtaxiasANHEIM, Mathieu; TRANCHANT, Christine; KOENIG, Michel et al.The New England journal of medicine. 2012, Vol 366, Num 7, pp 636-646, issn 0028-4793, 11 p.Article

Prospective clinical study of Writer's crampJEDYNAK, Pierre C; TRANCHANT, Christine; ZEGERS DE BEYL, Diederik et al.Movement disorders. 2001, Vol 16, Num 3, pp 494-499, issn 0885-3185Article

Long-term Outcomes of CLIPPERS (Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids) in a Consecutive Series of 12 PatientsTAIEB, Guillaume; DUFLOS, Claire; LEFAUCHEUR, Romain et al.Archives of neurology (Chicago). 2012, Vol 69, Num 7, pp 847-855, issn 0003-9942, 9 p.Article

Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops : A temporal study in man. CommentaryAPPEL, Stanley H; ECHANIZ-LAGUNA, Andoni; ZOLL, Jeffrey et al.Experimental neurology (Print). 2006, Vol 198, Num 1, issn 0014-4886, 1-3,25-30 [9 p.]Article

PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European populationMENERET, Aurélie; GRABLI, David; ANHEIM, Mathieu et al.Neurology. 2012, Vol 79, Num 2, pp 170-174, issn 0028-3878, 5 p.Article

Molecular diversity and gene expression of cotton ERF transcription factors reveal that group IXa members are responsive to jasmonate, ethylene and XanthomonasCHAMPION, Antony; HEBRARD, Eugenie; PARRA, Benoit et al.Molecular plant pathology. 2009, Vol 10, Num 4, pp 471-485, issn 1464-6722, 15 p.Article

Novel LAMP-2 gene mutation and successful treatment with heart transplantation in a large family with danon diseaseECHANIZ-LAGUNA, Andoni; MOHR, Michel; EPAILLY, Eric et al.Muscle & nerve. 2006, Vol 33, Num 3, pp 393-397, issn 0148-639X, 5 p.Article

Treatment of myasthenia gravis exacerbation with intravenous immunoglobulin : A randomized double-blind clinical trialGAJDOS, Philippe; TRANCHANT, Christine; CLAIR, Bernard et al.Archives of neurology (Chicago). 2005, Vol 62, Num 11, pp 1689-1693, issn 0003-9942, 5 p.Article

Singular DYT6 Phenotypes in Association with New THAP1 Frameshift MutationsBLANCHARD, Arnaud; ROUBERTIE, Agathe; BURBAUD, Pierre et al.Movement disorders. 2011, Vol 26, Num 9, pp 1775-1777, issn 0885-3185, 3 p.Article

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular DystrophyGUENEAU, Lucie; BERTRAND, Anne T; TRANCHANT, Christine et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 338-353, issn 0002-9297, 16 p.Article

ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q₁₀ DeficiencyLAGIER-TOURENNE, Clotilde; TAZIR, Meriem; ANHEIM, Mathieu et al.American journal of human genetics. 2008, Vol 82, Num 3, pp 661-672, issn 0002-9297, 12 p.Article

Mutations in SPGII are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degenerationSTEVANIN, Giovanni; AZZEDINE, Hamid; LOUREIRO, José et al.Brain. 2008, Vol 131, pp 772-784, issn 0006-8950, 13 p., 3Article

Development of a french isometric strength normative database for adults using quantitative muscle testingHOGREL, Jean-Yves; PAYAN, Christine A; TRANCHANT, Christine et al.Archives of physical medicine and rehabilitation. 2007, Vol 88, Num 10, pp 1289-1297, issn 0003-9993, 9 p.Article

Epidemiologic studies of environmental exposures in Parkinson's diseaseELBAZ, Alexis; TRANCHANT, Christine.Journal of the neurological sciences. 2007, Vol 262, Num 1-2, pp 37-44, issn 0022-510X, 8 p.Article

A study of three patients with amyotrophic lateral sclerosis and a polyneuropathy resembling CIDPECHANIZ-LAGUNA, Andoni; DEGOS, Bertrand; MOHR, Michel et al.Muscle & nerve. 2006, Vol 33, Num 3, pp 356-362, issn 0148-639X, 7 p.Article

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardationMALLARET, Martial; SYNOFZIK, Matthis; TRANCHANT, Christine et al.Brain. 2014, Vol 137, pp 411-419, issn 0006-8950, 9 p., 2Article

Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseasesMARCEL, Christophe; ANHEIM, Mathieu; FLAMAND-ROUVIERE, Constance et al.Journal of neurology. 2010, Vol 257, Num 8, pp 1369-1372, issn 0340-5354, 4 p.Article

Cognitive Functions in Neuromyelitis OpticaBLANC, Frédéric; ZEPHIR, Hélène; DE SEZE, Jérome et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 84-88, issn 0003-9942, 5 p.Article

Muscle nogo-A expression is a prognostic marker in lower motor neuron syndromesPRADAT, Pierre-Francois; BRUNETEAU, Gaelle; TRANCHANT, Christine et al.Annals of neurology. 2007, Vol 62, Num 1, pp 15-20, issn 0364-5134, 6 p.Article

Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron diseaseECHANIZ-LAGUNA, Andoni; GUIRAUD-CHAUMEIL, Christophe; TRANCHANT, Christine et al.Journal of neurology. 2002, Vol 249, Num 3, pp 290-293, issn 0340-5354Article