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Items: 1 to 20 of 32

1.

[Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families].

Dubourg O, Dürr A, Chneiweiss H, Stevanin G, Cancel G, Penet C, Agid Y, Brice A.

Rev Neurol (Paris). 1995 Nov;151(11):657-60. French.

PMID:
8745629
2.

[Molecular basis of heterogeneities of clinical presentation of dentatorubral pallidoluysian atrophy (DRPLA)].

Tsuji S.

Rinsho Shinkeigaku. 1994 Dec;34(12):1227-9. Review. Japanese.

PMID:
7774119
3.

Molecular pathology of dentatorubral-pallidoluysian atrophy.

Kanazawa I.

Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1069-74. Review.

4.

Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease.

Kanazawa I.

Neurogenetics. 1998 Dec;2(1):1-17. Review.

PMID:
9933295
5.

[Hereditary dentatorubro-pallidoluysian atrophy (DRPLA): clinical studies on 45 cases].

Yuasa T.

Nihon Rinsho. 1993 Nov;51(11):3016-23. Review. Japanese.

PMID:
8277585
6.

[Triplet repeat disorder, dentatorubral and pallidoluysian atrophy DRPLA)].

Yamada M.

Nihon Rinsho. 1995 Apr;53(4):1024-32. Review. Japanese.

PMID:
7752462
7.

[Somatic mosaicism of CAG repeats size in the nervous system of dentatorubral-pallidoluysian atrophy (DRPLA)].

Ito Y, Tanaka F, Sobue G.

Nihon Rinsho. 1999 Apr;57(4):850-5. Review. Japanese.

PMID:
10222778
8.

Hereditary dentatorubral-pallidoluysian atrophy.

Oyanagi S.

Neuropathology. 2000 Sep;20 Suppl:S42-6. Review.

PMID:
11037186
9.
10.

Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees.

Becher MW, Rubinsztein DC, Leggo J, Wagster MV, Stine OC, Ranen NG, Franz ML, Abbott MH, Sherr M, MacMillan JC, Barron L, Porteous M, Harper PS, Ross CA.

Mov Disord. 1997 Jul;12(4):519-30. Review.

PMID:
9251070
11.

Dentatorubral-pallidoluysian atrophy.

Tsuji S.

Handb Clin Neurol. 2012;103:587-94. doi: 10.1016/B978-0-444-51892-7.00041-3. Review.

PMID:
21827919
12.

Dentatorubral-pallidoluysian atrophy (DRPLA).

Tsuji S.

J Neural Transm Suppl. 2000;(58):167-80. Review.

PMID:
11128606
13.
14.

Dynamic mutation and human disorders: the spinocerebellar ataxias (review).

Costa Lima MA, Pimentel MM.

Int J Mol Med. 2004 Feb;13(2):299-302. Review.

PMID:
14719138
15.

[Dentatorubral-pallidoluysian atrophy (DRPLA: differential diagnosis of chorea)].

Tsuji S.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):101-3. Review. Japanese. No abstract available.

PMID:
10434603
16.

[SCA17, a novel polyglutamine disease caused by the expansion of polyglutamine tracts in TATA-binding protein].

Nakamura K.

Rinsho Shinkeigaku. 2001 Dec;41(12):1123-5. Review. Japanese.

PMID:
12235815
17.

[Autosomal dominant spinocerebellar ataxia].

Legros B, Manto MU.

Rev Med Brux. 1999 Dec;20(6):495-503. Review. French.

PMID:
10672773
18.

Autosomal dominant spinocerebellar atrophy with retinal degeneration.

Ptácek LJ.

Clin Neurosci. 1995;3(1):28-32. Review.

PMID:
7614091
19.

[Cloning and characterization of cDNA for DRPLA interacting protein].

Okamumoho Y, Yamada M.

Nihon Rinsho. 1999 Apr;57(4):856-61. Review. Japanese.

PMID:
10222779
20.

Dominantly inherited ataxias.

Subramony SH, Vig PJ, McDaniel DO.

Semin Neurol. 1999;19(4):419-25. Review.

PMID:
10716664

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