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Items: 1 to 20 of 103

1.

Ataxia, chorea, seizures, and dementia. Pathologic features of a newly defined familial disorder.

Farmer TW, Wingfield MS, Lynch SA, Vogel FS, Hulette C, Katchinoff B, Jacobson PL.

Arch Neurol. 1989 Jul;46(7):774-9.

PMID:
2742549
2.

Familial chorea and myoclonus epilepsy.

Takahata N, Ito K, Yoshimura Y, Nishihori K, Suzuki H.

Neurology. 1978 Sep;28(9 Pt 1):913-9.

PMID:
99688
3.
4.

Familial essential ("benign") chorea.

Bird TD, Carlson CB, Hall JG.

J Med Genet. 1976 Oct;13(5):357-62.

5.

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.

Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, Ruggiero G, Bonavita V, Masters C, Casari G, Bruni A.

Neurology. 2002 Mar 26;58(6):922-8.

PMID:
11914409
6.

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
7.

A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

Nelson I, Hanna MG, Alsanjari N, Scaravilli F, Morgan-Hughes JA, Harding AE.

Ann Neurol. 1995 Mar;37(3):400-3.

PMID:
7695240
8.

[(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
9.
10.

Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions.

Walker RH, Morgello S, Davidoff-Feldman B, Melnick A, Walsh MJ, Shashidharan P, Brin MF.

Neurology. 2002 Apr 9;58(7):1031-7.

PMID:
11940688
11.

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
12.

Autosomal dominant sensory ataxia: a neuroaxonal dystrophy.

Moeller JJ, Macaulay RJ, Valdmanis PN, Weston LE, Rouleau GA, Dupré N.

Acta Neuropathol. 2008 Sep;116(3):331-6. doi: 10.1007/s00401-008-0362-6. Epub 2008 Mar 18.

PMID:
18347805
13.
14.

A case of frontotemporal dementia and parkinsonism of early onset with progressive supranuclear palsy-like features.

Miyamoto K, Ikemoto A, Akiguchi I, Kohno R, Imura T, Fujita Y.

Clin Neuropathol. 2001 Jan-Feb;20(1):8-12.

PMID:
11220696
15.

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.

Kertesz A, Kawarai T, Rogaeva E, St George-Hyslop P, Poorkaj P, Bird TD, Munoz DG.

Neurology. 2000 Feb 22;54(4):818-27.

PMID:
10690970
16.

Dentatorubropallidoluysian atrophy: clinicopathological study of dementia and involvement of the nucleus basalis of Meynert in seven autopsy cases.

Tsuchiya K, Oyanagi S, Arima K, Ikeda K, Akashi T, Ando S, Kurosawa T, Ikeuchi T, Tsuji S.

Acta Neuropathol. 1998 Nov;96(5):502-8.

PMID:
9829814
17.

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
18.

FAME 3: a novel form of progressive myoclonus and epilepsy.

Carr JA, van der Walt PE, Nakayama J, Fu YH, Corfield V, Brink P, Ptacek L.

Neurology. 2007 Apr 24;68(17):1382-9.

PMID:
17452583
19.

Synapses in the hereditary ataxias.

Koeppen AH, Dickson AC, Lamarche JB, Robitaille Y.

J Neuropathol Exp Neurol. 1999 Jul;58(7):748-64.

PMID:
10411345
20.

Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau gene.

Miyamoto K, Kowalska A, Hasegawa M, Tabira T, Takahashi K, Araki W, Akiguchi I, Ikemoto A.

Ann Neurol. 2001 Jul;50(1):117-20.

PMID:
11456301

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