296 related articles for article (PubMed ID: 7877879)
41. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
42. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH
Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570
[TBL] [Abstract][Full Text] [Related]
43. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
Gomez CM; Thompson RM; Gammack JT; Perlman SL; Dobyns WB; Truwit CL; Zee DS; Clark HB; Anderson JH
Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
[TBL] [Abstract][Full Text] [Related]
44. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
Belal S; Cancel G; Stevanin G; Hentati F; Khati C; Ben Hamida C; Auburger G; Agid Y; Ben Hamida M; Brice A
Neurology; 1994 Aug; 44(8):1423-6. PubMed ID: 8058142
[TBL] [Abstract][Full Text] [Related]
45. Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.
Keats BJ; Pollack MS; McCall A; Wilensky MA; Ward LJ; Lu M; Zoghbi HY
Am J Hum Genet; 1991 Nov; 49(5):972-7. PubMed ID: 1928103
[TBL] [Abstract][Full Text] [Related]
46. Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.
Ranum LP; Rich SS; Nance MA; Duvick LA; Aita JF; Orr HT; Anton-Johnson S; Schut LJ
Neurology; 1992 Feb; 42(2):344-7. PubMed ID: 1736163
[TBL] [Abstract][Full Text] [Related]
47. Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.
Gouw LG; Kaplan CD; Haines JH; Digre KB; Rutledge SL; Matilla A; Leppert M; Zoghbi HY; Ptácek LJ
Nat Genet; 1995 May; 10(1):89-93. PubMed ID: 7647799
[TBL] [Abstract][Full Text] [Related]
48. [Overview of Hereditary Spinocerebellar Ataxias in Japan].
Tada M; Yokoseki A; Onodera O
Brain Nerve; 2017 Aug; 69(8):879-890. PubMed ID: 28819072
[TBL] [Abstract][Full Text] [Related]
49. Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05.
Volz A; Fonatsch C; Ziegler A
Cytogenet Cell Genet; 1992; 60(1):37-9. PubMed ID: 1582256
[TBL] [Abstract][Full Text] [Related]
50. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
Carson WJ; Radvany J; Farrer LA; Vincent D; Rosenberg RN; MacLeod PM; Rouleau GA
Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414
[TBL] [Abstract][Full Text] [Related]
51. [Chronic ataxia in childhood].
Erazo Torricelli R
Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
[TBL] [Abstract][Full Text] [Related]
52. Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1.
Shrimpton AE; Davidson R; MacDonald N; Brock DJ
J Med Genet; 1993 Jul; 30(7):616-7. PubMed ID: 8411042
[TBL] [Abstract][Full Text] [Related]
53. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Brkanac Z; Bylenok L; Fernandez M; Matsushita M; Lipe H; Wolff J; Nochlin D; Raskind WH; Bird TD
Arch Neurol; 2002 Aug; 59(8):1291-5. PubMed ID: 12164726
[TBL] [Abstract][Full Text] [Related]
54. Prevalence of inherited ataxias in the province of Padua, Italy.
Zortea M; Armani M; Pastorello E; Nunez GF; Lombardi S; Tonello S; Rigoni MT; Zuliani L; Mostacciuolo ML; Gellera C; Di Donato S; Trevisan CP
Neuroepidemiology; 2004; 23(6):275-80. PubMed ID: 15297793
[TBL] [Abstract][Full Text] [Related]
55. Current concepts in the treatment of hereditary ataxias.
Braga Neto P; Pedroso JL; Kuo SH; Marcondes Junior CF; Teive HA; Barsottini OG
Arq Neuropsiquiatr; 2016 Mar; 74(3):244-52. PubMed ID: 27050855
[TBL] [Abstract][Full Text] [Related]
56. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12.
Nechiporuk A; Lopes-Cendes I; Nechiporuk T; Starkman S; Andermann E; Rouleau GA; Weissenbach JS; Kort E; Pulst SM
Neurology; 1996 Jun; 46(6):1731-5. PubMed ID: 8649579
[TBL] [Abstract][Full Text] [Related]
57. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.
Lezin A; Cancel G; Stevanin G; Smadja D; Vernant JC; Dürr A; Martial J; Buisson GG; Bellance R; Chneiweiss H; Agid Y; Brice A
Hum Genet; 1996 May; 97(5):671-6. PubMed ID: 8655151
[TBL] [Abstract][Full Text] [Related]
58. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
Hirano R; Takashima H; Okubo R; Tajima K; Okamoto Y; Ishida S; Tsuruta K; Arisato T; Arata H; Nakagawa M; Osame M; Arimura K
Neurogenetics; 2004 Dec; 5(4):215-21. PubMed ID: 15455264
[TBL] [Abstract][Full Text] [Related]
59. Spinocerebellar ataxia type 31 exists in northeast China.
Ouyang Y; He Z; Li L; Qin X; Zhao Y; Yuan L
J Neurol Sci; 2012 May; 316(1-2):164-7. PubMed ID: 22353852
[TBL] [Abstract][Full Text] [Related]
60. Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1.
Hernández A; Magariño C; Gispert S; Santos N; Lunkes A; Orozco G; Heredero L; Beckmann J; Auburger G
Genomics; 1995 Jan; 25(2):433-5. PubMed ID: 7789976
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]