Traitement des ataxies cérébelleuses à anticorps anti-GAD par cures séquentielles de corticoïdes = Steroid treatment in four cases of anti-GAD cerebellar ataxiaBONNAN, M; CABRE, P; OLINDO, S et al.Revue neurologique (Paris). 2008, Vol 164, Num 5, pp 427-433, issn 0035-3787, 7 p.Article

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article

A kindred with cerebellar ataxia and thermoanalgesiaGENIS, D; FERRER, I; MARQUEZ, F et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 5, pp 518-523, issn 0022-3050, 6 p.Article

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1DUPRE, Nicolas; GROS-LOUIS, Francois; CHRESTIAN, Nicolas et al.Annals of neurology. 2007, Vol 62, Num 1, pp 93-98, issn 0364-5134, 6 p.Article

Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3HORVATH, Rita; CZERMIN, Birgit; BRODHUN, Michael et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 2, pp 174-178, issn 0022-3050, 5 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

Cerebellar ataxia with progressive improvementTSAO, Jack W; NEAL, Jason; APSE, Kira et al.Archives of neurology (Chicago). 2006, Vol 63, Num 4, pp 594-597, issn 0003-9942, 4 p.Article

Isolated gait ataxia due to cerebellar vermis infarctSURAJ ASHOK MULEY; BUSHARA, Khalafalla O.Archives of neurology (Chicago). 2004, Vol 61, Num 9, issn 0003-9942, p. 1461Article

Republished: A practical approac to late-onset cerebellar ataxia: putting the disorder with lack of order into orderVAN GAALEN, Judith; VAN DE WARRENBURG, Bart P.C.Postgraduate medical journal. 2012, Vol 88, Num 1041, pp 407-417, issn 0032-5473, 11 p.Article

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaBRUSSINO, A; GELLERA, C; MIGONE, N et al.Neurology. 2005, Vol 64, Num 1, pp 145-147, issn 0028-3878, 3 p.Article

Falls in degenerative cerebellar ataxiasVAN DE WARRENBURG, Bart P. C; STEIJNS, Janneke A. G; MUNNEKE, Marten et al.Movement disorders. 2005, Vol 20, Num 4, pp 497-500, issn 0885-3185, 4 p.Article

Decreased cerebellar total creatine in episodic ataxia type 2: A ¹H MRS studyHARNO, H; HEIKKINEN, S; KAUNISTO, M. A et al.Neurology. 2005, Vol 64, Num 3, pp 542-544, issn 0028-3878, 3 p.Article

Ataxie spastique autosomique récessive de Charlevoix-Saguenay : étude d'une famille et revue de la littérature = Autosomal recessive spastic ataxia of Charlevoix-Saguenay : Study of a family and review of the literatureANHEIM, M; CHAIGNE, D; FLEURY, M et al.Revue neurologique (Paris). 2008, Vol 164, Num 4, pp 363-368, issn 0035-3787, 6 p.Article

Ataxie cérébelleuse révélant un syndrome de Wolfram = Wolfram's syndrome presenting as a cerebellar ataxiaMATHIS, S; PAQUIS, V; MESNAGE, V et al.Revue neurologique (Paris). 2007, Vol 163, Num 2, pp 197-204, issn 0035-3787, 8 p.Article

Association d'un hypogonadisme hypogonadotrope et d'une ataxie cérébelleuse chez un homme : à propos d'un cas = Hypogonadotropic hypogonadism discovered in a patient with cerebellar ataxiaROBIN, G; JONARD, S; VUILLAUME, I et al.Annales d'endocrinologie. 2005, Vol 66, Num 6, pp 545-551, issn 0003-4266, 7 p.Article

Le mystère des protéines prions : des maladies neurodégénératives à la biologie de la reproduction = The mystery of prion proteins : from neurodegenerative diseases to the biology of reproductionPEOC'H, K.Annales de biologie clinique (Paris). 2005, Vol 63, Num 2, pp 121-126, issn 0003-3898, 6 p.Article

Une nouvelle forme d'ataxie récessive causée par des mutations du gène SYNE-1 = Mutations in SYNE-I lead to a newly discovered form of autosomal recessive cerebellar ataxiaDUPRE, Nicolas; BOUCHARD, Jean-Pierre; GROS-LOUIS, Francois et al.MS. Médecine sciences. 2007, Vol 23, Num 3, pp 261-262, issn 0767-0974, 2 p.Article

Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in JapaneseONODERA, Y; AOKI, M; MIZUNO, H et al.Neurology. 2006, Vol 67, Num 7, pp 1300-1302, issn 0028-3878, 3 p.Article

Cerebellar ataxia and central nervous system whipple diseaseMATTHEWS, Brandy R; JONES, Lyell K; SAAD, Dahlia A et al.Archives of neurology (Chicago). 2005, Vol 62, Num 4, pp 618-620, issn 0003-9942, 3 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

Atexia, delayed dentition and hypomyelination : A novel leukoencephalopathyWOLF, N. I; HALTING, I; BOLTSHAUSER, E et al.Neuropediatrics. 2007, Vol 38, Num 2, pp 64-70, issn 0174-304X, 7 p.Article

CSF analysis differentiates multiplesystem atrophy from idiopathic late-onset cerebellar ataxiaABDO, W. F; VAN DE WARRENBURG, B. P. C; MUNNEKE, M et al.Neurology. 2006, Vol 67, Num 3, pp 474-479, issn 0028-3878, 6 p.Article

Autoantibodies in postinfectious acute cerebellar ataxiaUCHIBORI, Ayumi; SAKUTA, Manabu; KUSUNOKI, Susumu et al.Neurology. 2005, Vol 65, Num 7, pp 1114-1116, issn 0028-3878, 3 p.Article

Late-onset pure cerebellar ataxia : Differentiating those with and without identifiable mutationsKERBER, Kevin A; JEN, Joanna C; PERLMAN, Susan et al.Journal of the neurological sciences. 2005, Vol 238, Num 1-2, pp 41-45, issn 0022-510X, 5 p.Article

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyVAN DE WARRENBURG, B. P. C; VERBEEK, D. S; PIERSMA, S. J et al.Neurology. 2003, Vol 61, Num 12, pp 1760-1765, issn 0028-3878, 6 p.Article