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9. Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease. Simon-Sanchez J; Hanson M; Singleton A; Hernandez D; McInerney A; Nussbaum R; Werner J; Gallardo M; Weiser R; Gwinn-Hardy K; Singleton AB; Clarimon J Neurosci Lett; 2005 Jul 1-8; 382(1-2):191-4. PubMed ID: 15911147 [TBL] [Abstract][Full Text] [Related]
10. Parkinson's disease, twins, and the DNA-damage hypothesis. Robbins JH Ann Neurol; 1987 Apr; 21(4):412. PubMed ID: 3579227 [No Abstract] [Full Text] [Related]
11. Extrahepatic biliary atresia in twins: zygosity determination by short tandem repeat loci. Poovorawan Y; Chongsrisawat V; Tanunytthawongse C; Norapaksunthorn T; Mutirangura A; Chandrakamol B J Med Assoc Thai; 1996 Dec; 79 Suppl 1():S119-24. PubMed ID: 9071076 [TBL] [Abstract][Full Text] [Related]
12. Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism? Charles P; Camuzat A; Benammar N; Sellal F; Destée A; Bonnet AM; Lesage S; Le Ber I; Stevanin G; Dürr A; Brice A; Neurology; 2007 Nov; 69(21):1970-5. PubMed ID: 17568014 [TBL] [Abstract][Full Text] [Related]
13. Delineation of the dystonia-parkinsonism syndrome locus in Xq13. Graeber MB; Kupke KG; Müller U Proc Natl Acad Sci U S A; 1992 Sep; 89(17):8245-8. PubMed ID: 1518853 [TBL] [Abstract][Full Text] [Related]
14. LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. Nichols WC; Elsaesser VE; Pankratz N; Pauciulo MW; Marek DK; Halter CA; Rudolph A; Shults CW; Foroud T; Neurology; 2007 Oct; 69(18):1737-44. PubMed ID: 17804834 [TBL] [Abstract][Full Text] [Related]
15. Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism. Hardy J; Pérez-Tur J; Baker M; Farrer M; Crook R; Hutton M; Johnson WG; Gwinn K; Muenter M; Rocca WA; Maraganore D Am J Med Genet; 1998 Mar; 81(2):166-71. PubMed ID: 9613857 [TBL] [Abstract][Full Text] [Related]
16. Discordant identical twins. II. Parkinsonism. Pembrey ME Practitioner; 1972 Aug; 209(250):240-3. PubMed ID: 5078238 [No Abstract] [Full Text] [Related]
17. [Juvenile parkinsonism in monozygotic twins]. Umehara F; Nomoto M; Usuki F; Matsumoto W; Osame M Rinsho Shinkeigaku; 1991 Mar; 31(3):306-9. PubMed ID: 1893671 [TBL] [Abstract][Full Text] [Related]
18. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2. Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117 [TBL] [Abstract][Full Text] [Related]
19. Genetic susceptibility to Parkinson's disease. Johnson WG Geriatrics; 1991 Aug; 46 Suppl 1():52-9. PubMed ID: 1894147 [TBL] [Abstract][Full Text] [Related]
20. The role of inheritance in sporadic Parkinson's disease. Hawkes C Ann Neurol; 2000 May; 47(5):682. PubMed ID: 10805345 [No Abstract] [Full Text] [Related] [Next] [New Search]