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- [1] Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management[J]. NEUROGENETICS, 2010, 11 (01) : 1 - 12Anheim, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, France ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceFleury, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceMonga, B.论文数: 0 引用数: 0 h-index: 0机构: ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France Univ Lubumbashi, Fac Med, Lubumbashi, DEM REP CONGO CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceLaugel, V.论文数: 0 引用数: 0 h-index: 0机构: Hop Hautepierre, Dept Pediat, Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceChaigne, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Hautepierre, Dept Pediat, Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceRodier, G.论文数: 0 引用数: 0 h-index: 0机构: Hop E Muller, Dept Neurol, Mulhouse, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceGinglinger, E.论文数: 0 引用数: 0 h-index: 0机构: Hop Hasenrain, Lab Diagnost Genet, Mulhouse, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceBoulay, C.论文数: 0 引用数: 0 h-index: 0机构: Hop E Muller, Dept Neurol, Mulhouse, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceCourtois, S.论文数: 0 引用数: 0 h-index: 0机构: Hop E Muller, Dept Neurol, Mulhouse, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceDrouot, N.论文数: 0 引用数: 0 h-index: 0机构: ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceFritsch, M.论文数: 0 引用数: 0 h-index: 0机构: Nouvel Hop Civil, Lab Diagnost Genet, Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceDelaunoy, J. P.论文数: 0 引用数: 0 h-index: 0机构: Nouvel Hop Civil, Lab Diagnost Genet, Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceStoppa-Lyonnet, D.论文数: 0 引用数: 0 h-index: 0机构: Inst Curie, Serv Genet, Dept Biol, Paris, France Univ Paris 05, Paris, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceTranchant, C.论文数: 0 引用数: 0 h-index: 0机构: CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, France ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, FranceKoenig, M.论文数: 0 引用数: 0 h-index: 0机构: ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France Nouvel Hop Civil, Lab Diagnost Genet, Strasbourg, France CHU Strasbourg, Hop Civil, Dept Neurol, F-67000 Strasbourg, France
- [2] ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia[J]. NEUROGENETICS, 2008, 9 (03) : 207 - 214Vermeer, Sascha论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsMeijer, Rowdy P. P.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsPijl, Benjamin J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsTimmermans, Janneke论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Cardiol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsCruysberg, Johannes R. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Ophthalmol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsBos, Maaike M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsSchelhaas, Helenius J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlandsvan de Warrenburg, Bart P. C.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKnoers, Nine V. A. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsScheffer, Hans论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsKremer, Berry论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6525 ED Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands