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Items: 6

1.

Pathological accumulation of atrophin-1 in dentatorubralpallidoluysian atrophy.

Suzuki Y, Yazawa I.

Int J Clin Exp Pathol. 2011 Apr;4(4):378-84. Epub 2011 Apr 25. Review.

2.

Severe neurological phenotypes of Q129 DRPLA transgenic mice serendipitously created by en masse expansion of CAG repeats in Q76 DRPLA mice.

Sato T, Miura M, Yamada M, Yoshida T, Wood JD, Yazawa I, Masuda M, Suzuki T, Shin RM, Yau HJ, Liu FC, Shimohata T, Onodera O, Ross CA, Katsuki M, Takahashi H, Kano M, Aosaki T, Tsuji S.

Hum Mol Genet. 2009 Feb 15;18(4):723-36. doi: 10.1093/hmg/ddn403. Epub 2008 Nov 27.

3.

Young onset dementia.

Sampson EL, Warren JD, Rossor MN.

Postgrad Med J. 2004 Mar;80(941):125-39. Review.

4.

A sporadic case of dentatorubral pallidoluysian atrophy (DRPLA) with CAG repeat expansion but no clinical abnormalities in the father.

Shimizu N, Yamami T, Nakayama M, Ikeuchi T, Koide R, Tsuji S.

J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):113-4. No abstract available.

5.

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability.

Takano H, Onodera O, Takahashi H, Igarashi S, Yamada M, Oyake M, Ikeuchi T, Koide R, Tanaka H, Iwabuchi K, Tsuji S.

Am J Hum Genet. 1996 Jun;58(6):1212-22.

6.

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I.

J Med Genet. 1990 Feb;27(2):105-8.

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