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46. 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. PubMed ID: 9251070 [TBL] [Abstract][Full Text] [Related]
47. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case. Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805 [TBL] [Abstract][Full Text] [Related]
48. 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. PubMed ID: 7868125 [TBL] [Abstract][Full Text] [Related]
49. Rapidly progressive sporadic dentatorubral pallidoluysian atrophy with intracytoplasmic inclusions and no CAG repeat expansion. Espay AJ; Bergeron C; Chen R; Lang AE Mov Disord; 2006 Dec; 21(12):2251-4. PubMed ID: 17078058 [TBL] [Abstract][Full Text] [Related]
50. [Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types]. Takeda S; Takahashi H; Ikuta F No To Shinkei; 1992 Feb; 44(2):111-6. PubMed ID: 1567729 [TBL] [Abstract][Full Text] [Related]
51. [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. PubMed ID: 8745629 [TBL] [Abstract][Full Text] [Related]
52. Sporadic case of dentatorubral pallidoluysian atrophy with no CAG repeat expansion and no intranuclear inclusions. Munhoz RP; Bergeron C; Lang AE Mov Disord; 2004 May; 19(5):580-3. PubMed ID: 15133824 [TBL] [Abstract][Full Text] [Related]
57. Different patterns of [18F]dopa uptake in siblings with hereditary dentato-rubro-pallido-luysian atrophy. Minami T; Otsuka M; Ichiya Y; Nomura A; Ueda K Brain Dev; 1994; 16(4):335-8. PubMed ID: 7818032 [TBL] [Abstract][Full Text] [Related]
58. Coexistence of dentatorubral-pallidoluysian atrophy and Parkinson's disease: An autopsy case report. Kim SI; Kim H; Park JW; Choi JH; Kim HJ; Won JK; Jeon B; Park SH Neuropathology; 2021 Jun; 41(3):196-205. PubMed ID: 33851459 [TBL] [Abstract][Full Text] [Related]
59. 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 Neurology; 1995 Jan; 45(1):143-9. PubMed ID: 7824105 [TBL] [Abstract][Full Text] [Related]
60. Dentatorubropallidoluysian atrophy in a spanish family: a clinical, radiological, pathological, and genetic study. Muñoz E; Milà M; Sánchez A; Latorre P; Ariza A; Codina M; Ballesta F; Tolosa E J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):811-4. PubMed ID: 10567506 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]