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Items: 14

1.

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
2.

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
3.

Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.

Warner TT, Lennox GG, Janota I, Harding AE.

Mov Disord. 1994 May;9(3):289-96.

PMID:
8041369
4.

DRPLA in Europe.

Warner TT, Williams L, Harding AE.

Nat Genet. 1994 Mar;6(3):225. No abstract available.

PMID:
8012381
5.

B37 repeats are normal in most schizophrenic patients.

Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA, Ross CA, Li SH, Lofthouse R, Crow TJ, DeLisi LE.

Br J Psychiatry. 1994 Jun;164(6):851-2. No abstract available.

PMID:
7953005
6.

The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family.

Burke JR, Wingfield MS, Lewis KE, Roses AD, Lee JE, Hulette C, Pericak-Vance MA, Vance JM.

Nat Genet. 1994 Aug;7(4):521-4.

PMID:
7951323
7.

Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy.

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

Hum Genet. 1995 Mar;95(3):313-8.

PMID:
7868125
8.

Molecular and clinical findings in a family with dentatorubral-pallidoluysian atrophy.

Potter NT, Meyer MA, Zimmerman AW, Eisenstadt ML, Anderson IJ.

Ann Neurol. 1995 Feb;37(2):273-7.

PMID:
7847869
9.

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA).

Nagafuchi S, Yanagisawa H, Ohsaki E, Shirayama T, Tadokoro K, Inoue T, Yamada M.

Nat Genet. 1994 Oct;8(2):177-82.

PMID:
7842016
10.

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
11.

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
12.

Triplet repeats in clinical subtypes of schizophrenia: variation at the DRPLA (B 37 CAG repeat) locus is not associated with periodic catatonia.

Lesch KP, Stöber G, Balling U, Franzek E, Li SH, Ross CA, Newman M, Beckmann H, Riederer P.

J Neural Transm Gen Sect. 1994;98(2):153-7.

PMID:
7734112
13.

A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families.

Warner TT, Williams LD, Walker RW, Flinter F, Robb SA, Bundey SE, Honavar M, Harding AE.

Ann Neurol. 1995 Apr;37(4):452-9.

PMID:
7717681
14.

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA).

Ueno S, Kondoh K, Kotani Y, Komure O, Kuno S, Kawai J, Hazama F, Sano A.

Hum Mol Genet. 1995 Apr;4(4):663-6.

PMID:
7633415
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