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Items: 1 to 20 of 145

1.

Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathologic variants in a family.

Takahashi H, Ohama E, Naito H, Takeda S, Nakashima S, Makifuchi T, Ikuta F.

Neurology. 1988 Jul;38(7):1065-70.

PMID:
3386824
2.

[Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].

Miyashita K, Inuzuka T, Ishikawa A, Kondo H, Kawakami A, Takeda S, Ikuta F, Yuasa T.

No To Shinkei. 1992 Mar;44(3):279-84. Japanese.

PMID:
1591106
3.

[(Neurological CPC.55). A 60-year-old woman with progressive cerebellar ataxia, myoclonus, and dementia].

Morikawa N, Mori H, Sumino S, Kodera M, Shirai T, Kondo T, Mizuno Y.

No To Shinkei. 1997 Jul;49(7):663-71. Japanese.

PMID:
9234257
4.

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T, et al.

Ann Neurol. 1995 Jun;37(6):769-75.

PMID:
7778850
5.

Anticipation in hereditary dentatorubral-pallidoluysian atrophy.

Sano A, Yamauchi N, Kakimoto Y, Komure O, Kawai J, Hazama F, Kuzume K, Sano N, Kondo I.

Hum Genet. 1994 Jun;93(6):699-702.

PMID:
8005597
6.

Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy.

Suzuki S, Kamoshita S, Ninomura S.

Pediatr Neurol. 1985 Sep-Oct;1(5):298-301.

PMID:
3880416
7.

Juvenile dentatorubral-pallidoluysian atrophy: new clinical features.

Licht DJ, Lynch DR.

Pediatr Neurol. 2002 Jan;26(1):51-4.

PMID:
11814736
8.

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

Yuasa T.

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

PMID:
8277585
10.

Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia.

Le Ber I, Camuzat A, Castelnovo G, Azulay JP, Genton P, Gastaut JL, Broglin D, Labauge P, Brice A, Durr A.

Arch Neurol. 2003 Aug;60(8):1097-9.

PMID:
12925365
11.

Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.

Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S.

Clin Neurosci. 1995;3(1):23-7.

PMID:
7614090
12.

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, et al.

Nat Genet. 1994 Jan;6(1):9-13.

PMID:
8136840
13.

Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.

Nielsen JE, Sørensen SA, Hasholt L, Nørremølle A.

Mov Disord. 1996 Sep;11(5):533-41.

PMID:
8866494
14.

[A case of juvenile type dentatorubral-pallidoluysian atrophy (DRPLA) with psychomotor retardation since infancy].

Wada Y, Matsuoka T, Imai K, Taniike M, Mano T, Ono J, Okada S, Kondo I.

No To Hattatsu. 1998 Nov;30(6):543-8. Japanese.

PMID:
9844421
15.

[A sporadic dentatorubral-pallidoluysian atrophy (DRPLA) diagnosed by gene analysis].

Yoshimoto H, Sahara M, Tanaka K, Ikeuchi T, Koide R, Tsuji S.

Rinsho Shinkeigaku. 1995 Feb;35(2):201-3. Japanese.

PMID:
7781240
16.

Hereditary dentatorubral-pallidoluysian atrophy.

Oyanagi S.

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

PMID:
11037186
17.

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation.

Komure O, Sano A, Nishino N, Yamauchi N, Ueno S, Kondoh K, Sano N, Takahashi M, Murayama N, Kondo I, et al.

Neurology. 1995 Jan;45(1):143-9.

PMID:
7824105
18.

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.

Nagafuchi S, Yanagisawa H, Sato K, Shirayama T, Ohsaki E, Bundo M, Takeda T, Tadokoro K, Kondo I, Murayama N, et al.

Nat Genet. 1994 Jan;6(1):14-8.

PMID:
8136826
19.

[Genetic analysis including predictive DNA testing in a Japanese family with dentatorubral-pallidoluysian atrophy].

Nishio H, Wada H, Lee MJ, Matsuo T.

No To Hattatsu. 1998 Nov;30(6):512-6. Japanese.

PMID:
9844416
20.

Homozygosity for an allele carrying intermediate CAG repeats in the dentatorubral-pallidoluysian atrophy (DRPLA) gene results in spastic paraplegia.

Kurohara K, Kuroda Y, Maruyama H, Kawakami H, Yukitake M, Matsui M, Nakamura S.

Neurology. 1997 Apr;48(4):1087-90.

PMID:
9109905

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