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Results: 1 to 20 of 141

1.

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.

Dudding TE, Friend K, Schofield PW, Lee S, Wilkinson IA, Richards RI.

Neurology. 2004 Dec 28;63(12):2288-92.

PMID:
15623688
[PubMed - indexed for MEDLINE]
2.

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia.

Nagaoka U, Takashima M, Ishikawa K, Yoshizawa K, Yoshizawa T, Ishikawa M, Yamawaki T, Shoji S, Mizusawa H.

Neurology. 2000 May 23;54(10):1971-5.

PMID:
10822439
[PubMed - indexed for MEDLINE]
3.

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.

Chung MY, Lu YC, Cheng NC, Soong BW.

Brain. 2003 Jun;126(Pt 6):1293-9.

PMID:
12764052
[PubMed - indexed for MEDLINE]
Free Article
4.

Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.

Grewal RP, Tayag E, Figueroa KP, Zu L, Durazo A, Nunez C, Pulst SM.

Neurology. 1998 Nov;51(5):1423-6.

PMID:
9818872
[PubMed - indexed for MEDLINE]
5.

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S.

Neurology. 2004 Feb 24;62(4):648-51.

PMID:
14981189
[PubMed - indexed for MEDLINE]
6.

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F.

Neurology. 2000 Apr 11;54(7):1408-14.

PMID:
10751248
[PubMed - indexed for MEDLINE]
7.

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

Zu L, Figueroa KP, Grewal R, Pulst SM.

Am J Hum Genet. 1999 Feb;64(2):594-9.

PMID:
9973298
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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 8;114(4):450-7.

PMID:
11992570
[PubMed - indexed for MEDLINE]
9.

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant.

Knight MA, Kennerson ML, Anney RJ, Matsuura T, Nicholson GA, Salimi-Tari P, Gardner RJ, Storey E, Forrest SM.

Neurobiol Dis. 2003 Jul;13(2):147-57.

PMID:
12828938
[PubMed - indexed for MEDLINE]
10.

A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.

Miyoshi Y, Yamada T, Tanimura M, Taniwaki T, Arakawa K, Ohyagi Y, Furuya H, Yamamoto K, Sakai K, Sasazuki T, Kira J.

Neurology. 2001 Jul 10;57(1):96-100.

PMID:
11445634
[PubMed - indexed for MEDLINE]
11.

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. Erratum in: Arch Neurol 2002 Dec;59(12):1972.

PMID:
12164726
[PubMed - indexed for MEDLINE]
12.

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation.

Herman-Bert A, Stevanin G, Netter JC, Rascol O, Brassat D, Calvas P, Camuzat A, Yuan Q, Schalling M, Dürr A, Brice A.

Am J Hum Genet. 2000 Jul;67(1):229-35. Epub 2000 May 11.

PMID:
10820125
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Two Italian families with ITPR1 gene deletion presenting a broader phenotype of SCA15.

Di Gregorio E, Orsi L, Godani M, Vaula G, Jensen S, Salmon E, Ferrari G, Squadrone S, Abete MC, Cagnoli C, Brussino A, Brusco A.

Cerebellum. 2010 Mar;9(1):115-23. doi: 10.1007/s12311-009-0154-0.

PMID:
20082166
[PubMed - indexed for MEDLINE]
14.

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.

Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C, et al.

Nat Genet. 1993 Jul;4(3):295-9.

PMID:
8358438
[PubMed - indexed for MEDLINE]
15.

FAME 3: a novel form of progressive myoclonus and epilepsy.

Carr JA, van der Walt PE, Nakayama J, Fu YH, Corfield V, Brink P, Ptacek L.

Neurology. 2007 Apr 24;68(17):1382-9.

PMID:
17452583
[PubMed - indexed for MEDLINE]
16.

Cerebellar ataxia with progressive improvement.

Tsao JW, Neal J, Apse K, Stephan MJ, Dobyns WB, Hill RS, Walsh CA, Sheen VL.

Arch Neurol. 2006 Apr;63(4):594-7.

PMID:
16606775
[PubMed - indexed for MEDLINE]
17.

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.

Cagnoli C, Mariotti C, Taroni F, Seri M, Brussino A, Michielotto C, Grisoli M, Di Bella D, Migone N, Gellera C, Di Donato S, Brusco A.

Brain. 2006 Jan;129(Pt 1):235-42. Epub 2005 Oct 26.

PMID:
16251216
[PubMed - indexed for MEDLINE]
Free Article
18.

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.

Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A.

Ann Neurol. 2004 Jan;55(1):97-104.

PMID:
14705117
[PubMed - indexed for MEDLINE]
19.

Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.

Twells R, Yenchitsomanus PT, Sirinavin C, Allotey R, Poungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P, et al.

Hum Mol Genet. 1994 Jan;3(1):177-80.

PMID:
8162021
[PubMed - indexed for MEDLINE]
20.

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.

PMID:
8058142
[PubMed - indexed for MEDLINE]

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