Format
Sort by

Send to

Choose Destination

Links from Books

Items: 1 to 20 of 52

1.

Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease.

Kim JS, Son TO, Youn J, Ki CS, Cho JW.

J Clin Neurol. 2013 Oct;9(4):274-9. doi: 10.3988/jcn.2013.9.4.274. Epub 2013 Oct 31.

2.

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Ushe M, Perlmutter JS.

Mov Disord. 2012 Dec;27(14):1741-2. doi: 10.1002/mds.25295. No abstract available.

3.

Non-ATG-initiated translation directed by microsatellite expansions.

Zu T, Gibbens B, Doty NS, Gomes-Pereira M, Huguet A, Stone MD, Margolis J, Peterson M, Markowski TW, Ingram MA, Nan Z, Forster C, Low WC, Schoser B, Somia NV, Clark HB, Schmechel S, Bitterman PB, Gourdon G, Swanson MS, Moseley M, Ranum LP.

Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):260-5. doi: 10.1073/pnas.1013343108. Epub 2010 Dec 20.

4.

RNA gain-of-function in spinocerebellar ataxia type 8.

Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner TJ, Swanson MS, Ranum LP.

PLoS Genet. 2009 Aug;5(8):e1000600. doi: 10.1371/journal.pgen.1000600. Epub 2009 Aug 14.

5.

Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.

Gupta A, Jankovic J.

Parkinsonism Relat Disord. 2009 Nov;15(9):621-6. doi: 10.1016/j.parkreldis.2009.06.001. Epub 2009 Jun 25. Review.

PMID:
19559641
7.

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP.

Nat Genet. 2006 Jul;38(7):758-69. Epub 2006 Jun 25.

PMID:
16804541
8.

RNA-mediated neuromuscular disorders.

Ranum LP, Cooper TA.

Annu Rev Neurosci. 2006;29:259-77. Review.

PMID:
16776586
9.

Atypical parkinsonism and SCA8.

Munhoz RP, Teive HA, Raskin S, Troiano AR.

Parkinsonism Relat Disord. 2006 Apr;12(3):191-2. Epub 2005 Dec 20. No abstract available.

PMID:
16368257
10.

Early onset of ataxia in a child with a pathogenic SCA8 allele.

Felling RJ, Barron TF.

Pediatr Neurol. 2005 Aug;33(2):136-8. Review.

PMID:
16087061
11.

Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.

Maschke M, Oehlert G, Xie TD, Perlman S, Subramony SH, Kumar N, Ptacek LJ, Gomez CM.

Mov Disord. 2005 Nov;20(11):1405-12.

PMID:
16037936
12.

Cognitive impairment in spinocerebellar ataxia type 8.

Lilja A, Hämäläinen P, Kaitaranta E, Rinne R.

J Neurol Sci. 2005 Oct 15;237(1-2):31-8.

PMID:
15958266
13.

Sporadic SCA8 mutation resembling corticobasal degeneration.

Baba Y, Uitti RJ, Farrer MJ, Wszolek ZK.

Parkinsonism Relat Disord. 2005 May;11(3):147-50.

PMID:
15823478
14.

Giant SCA8 alleles in nine children whose mother has two moderately large ones.

Corral J, Genís D, Banchs I, San Nicolás H, Armstrong J, Volpini V.

Ann Neurol. 2005 Apr;57(4):549-53.

PMID:
15786481
15.

False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy.

Factor SA, Qian J, Lava NS, Hubbard JD, Payami H.

Ann Neurol. 2005 Mar;57(3):462-3. No abstract available.

PMID:
15732096
16.
17.

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.

Ikeda Y, Dalton JC, Moseley ML, Gardner KL, Bird TD, Ashizawa T, Seltzer WK, Pandolfo M, Milunsky A, Potter NT, Shoji M, Vincent JB, Day JW, Ranum LP.

Am J Hum Genet. 2004 Jul;75(1):3-16. Epub 2004 May 19.

18.

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.

Arch Neurol. 2004 May;61(5):727-33.

PMID:
15148151
19.

Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports.

Zeman A, Stone J, Porteous M, Burns E, Barron L, Warner J.

J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):459-65. Review.

20.

Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.

Sułek A, Hoffman-Zacharska D, Bednarska-Makaruk M, Szirkowiec W, Zaremba J.

J Appl Genet. 2004;45(1):101-5.

PMID:
14960773
Items per page

Supplemental Content

Write to the Help Desk