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Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disordersMANTUANO, E; VENEZIANO, L; JODICE, C et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 147-153, issn 1424-8581, 7 p.Article

Spinocerebellar ataxia 7 (SCA7)LEBRE, A.-S; BRICE, A.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 154-163, issn 1424-8581, 10 p.Article

The hereditary spinocerebellar ataxias in JapanSASAKI, H; YABE, I; TASHIRO, K et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 198-205, issn 1424-8581, 8 p.Article

Molecular genetics of spinocerebellar ataxia type 8 (SCA8)MOSEMILLER, A. K; DALTON, J. C; DAY, J. W et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 175-183, issn 1424-8581, 9 p.Article

Profile of families with Parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)FURTADO, Sarah; PAYAMI, Haydeh; DE LA FUENTE-FERNANDEZ, Raul et al.Movement disorders. 2004, Vol 19, Num 6, pp 622-629, issn 0885-3185, 8 p.Article

Molecular epidemiology of spinocerebellar ataxia type 6CRAIG, Kate; KEERS, Sharon M; ARCHIBALD, Kate et al.Annals of neurology. 2004, Vol 55, Num 5, pp 752-755, issn 0364-5134, 4 p.Article

Spinocerebellar ataxia type 5: Clinical and molecular genetic features of a German kindredBÜRK, K; ZÜHLKE, C; KÖNIG, I. R et al.Neurology. 2004, Vol 62, Num 2, pp 327-329, issn 0028-3878, 3 p.Article

Insights into the molecular basis of polyglutamine neurodegeneration from studies of a spinocerebellar ataxia type 7 mouse modelGROTE, S. K; LA SPADA, A. R.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 164-174, issn 1424-8581, 11 p.Article

The parkinsonian phenotype of spinocerebellar ataxia type 2LU, Chin-Song; CHOU, Yah-Huei Wu; KUO, Pei-Chi et al.Archives of neurology (Chicago). 2004, Vol 61, Num 1, pp 35-38, issn 0003-9942, 4 p.Article

Autosomal dominant cerebellar ataxias = Les ataxies cérébelleuses autosomiques dominantesMARELLI, C; CAZENEUVE, C; BRICE, A et al.Revue neurologique (Paris). 2011, Vol 167, Num 5, pp 385-400, issn 0035-3787, 16 p.Article

Molecular genetics of hereditary spinocerebellar ataxia: Mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian familiesBRUSCO, Alfredo; GELLERA, Cinzia; TARONI, Franco et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 727-733, issn 0003-9942, 7 p.Article

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10MATSUURA, Tohru; PING FANG; ZOGHBI, Huda Y et al.American journal of human genetics. 2004, Vol 74, Num 6, pp 1216-1224, issn 0002-9297, 9 p.Article

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in Spinocerebellar ataxia type 17ODA, Masaya; MARUYAMA, Hirofumi; MATSUMOTO, Masayasu et al.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 209-212, issn 0003-9942, 4 p.Article

Spinocerebellar ataxia type 17 in the Yugoslav populationALENDAR, A; CULJKOVIC, B; SAVIC, D et al.Acta neurologica scandinavica. 2004, Vol 109, Num 3, pp 185-187, issn 0001-6314, 3 p.Article

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in Western JapanTERASAWA, Hideo; ODA, Masaya; MORINO, Hiroyuki et al.Neuroscience letters. 2004, Vol 358, Num 2, pp 107-110, issn 0304-3940, 4 p.Article

Peripheral nerve involvement in spinocerebellar ataxiasVAN DE WARRENBURG, Bart P. C; NOTERMANS, Nicolette C; SCHELHAAS, Helenius J et al.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 257-261, issn 0003-9942, 5 p.Article

Spinocerebellar ataxia type 8: Molecular genetic comparisons and haplotype analysis of 37 families with ataxiaIKEDA, Yoshio; DALTON, Joline C; SHOJI, Mikio et al.American journal of human genetics. 2004, Vol 75, Num 1, pp 3-16, issn 0002-9297, 14 p.Article

Complex phenotypes in an Indian family with homozygous SCA2 mutationsRAGOTHAMAN, Mona; SARANGMATH, Nagaraja; THELMA, B. K et al.Annals of neurology. 2004, Vol 55, Num 1, pp 130-133, issn 0364-5134, 4 p.Article

Discoveries in sphingolipid metabolism, spinocerebellar ataxia and autoimmune diseaseBRUNHAM, Liam R; CHAN, Edmond Y. W; ORBAN, Paul C et al.Clinical genetics. 2003, Vol 64, Num 1, pp 1-6, issn 0009-9163, 6 p.Article

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pSTEVANIN, Giovanni; BOUSLAM, Naima; THOBOIS, Stéphane et al.Annals of neurology. 2004, Vol 55, Num 1, pp 97-104, issn 0364-5134, 8 p.Article

Electrophysiologic characterization in spinocerebellar ataxia 17MANGANELLI, F; PERRETTI, A; NOLANO, M et al.Neurology. 2006, Vol 66, Num 6, pp 932-934, issn 0028-3878, 3 p.Article

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2VELAZQUEZ-PEREZ, Luis; SEIFRIED, Carola; VELAZQUEZ-MANRESA, Mercedes et al.Annals of neurology. 2004, Vol 56, Num 3, pp 444-447, issn 0364-5134, 4 p.Article

Basal ganglia involvement of a patient with SCA 17: A new form of autosomal dominant spinocerebellar ataxiaGÜNTHER, P; STORCH, A; SCHWARZ, J et al.Journal of neurology. 2004, Vol 251, Num 7, pp 896-897, issn 0340-5354, 2 p.Article

Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of TaiwanTSAIL, H.-F; LIU, C.-S; LEU, T.-M et al.Acta neurologica scandinavica. 2004, Vol 109, Num 5, pp 355-360, issn 0001-6314, 6 p.Article

SCA12: An unusual mutation leads to an unusual spinocerebellar ataxiaHOLMES, Susan E; O'HEARN, Elizabeth; ROSS, Christopher A et al.Brain research bulletin. 2001, Vol 56, Num 3-4, pp 397-403, issn 0361-9230Conference Paper

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