155 related articles for article (PubMed ID: 2158268)
1. A large kindred with autosomal dominant Parkinson's disease.
Golbe LI; Di Iorio G; Bonavita V; Miller DC; Duvoisin RC
Ann Neurol; 1990 Mar; 27(3):276-82. PubMed ID: 2158268
[TBL] [Abstract][Full Text] [Related]
2. Clinical genetic analysis of Parkinson's disease in the Contursi kindred.
Golbe LI; Di Iorio G; Sanges G; Lazzarini AM; La Sala S; Bonavita V; Duvoisin RC
Ann Neurol; 1996 Nov; 40(5):767-75. PubMed ID: 8957018
[TBL] [Abstract][Full Text] [Related]
3. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
Gasser T; Müller-Myhsok B; Wszolek ZK; Oehlmann R; Calne DB; Bonifati V; Bereznai B; Fabrizio E; Vieregge P; Horstmann RD
Nat Genet; 1998 Mar; 18(3):262-5. PubMed ID: 9500549
[TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant Lewy body parkinsonism in a four-generation family.
Waters CH; Miller CA
Ann Neurol; 1994 Jan; 35(1):59-64. PubMed ID: 8285594
[TBL] [Abstract][Full Text] [Related]
5. A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.
Markopoulou K; Wszolek ZK; Pfeiffer RF
Ann Neurol; 1995 Sep; 38(3):373-8. PubMed ID: 7668822
[TBL] [Abstract][Full Text] [Related]
6. [Progress in the basic and clinical aspects of Parkinson's disease].
Mizuno Y
Rinsho Shinkeigaku; 2004 Nov; 44(11):741-50. PubMed ID: 15651281
[TBL] [Abstract][Full Text] [Related]
7. Clinical features of familial Parkinson's disease in Thai patients.
Prueksaritanond S; Boongird P; Pulkes T; Prueksaritanond S
Qual Prim Care; 2009; 17(2):115-22. PubMed ID: 19416604
[TBL] [Abstract][Full Text] [Related]
8. Young onset Parkinson's disease.
Quinn N; Critchley P; Marsden CD
Mov Disord; 1987; 2(2):73-91. PubMed ID: 3504266
[TBL] [Abstract][Full Text] [Related]
9. A clinical and genetic study of familial Parkinson's disease.
Maraganore DM; Harding AE; Marsden CD
Mov Disord; 1991; 6(3):205-11. PubMed ID: 1922124
[TBL] [Abstract][Full Text] [Related]
10. A clinical-genetic study of Parkinson's disease in a genetically isolated community.
Dekker MC; van Swieten JC; Houwing-Duistermaat JJ; Snijders PJ; Boeren E; Hofman A; Breteler MM; Heutink P; Oostra BA; van Duijn CM
J Neurol; 2003 Sep; 250(9):1056-62. PubMed ID: 14504966
[TBL] [Abstract][Full Text] [Related]
11. Genetic susceptibility to Parkinson's disease.
Johnson WG
Geriatrics; 1991 Aug; 46 Suppl 1():52-9. PubMed ID: 1894147
[TBL] [Abstract][Full Text] [Related]
12. The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies.
Golbe LI; Di Iorio G; Lazzarini A; Vieregge P; Gershanik OS; Bonavita V; Duvoisin RC
Adv Neurol; 1999; 80():165-70. PubMed ID: 10410717
[No Abstract] [Full Text] [Related]
13. Molecular genetics of Parkinson's disease.
Gasser T
Adv Neurol; 2001; 86():23-32. PubMed ID: 11553982
[TBL] [Abstract][Full Text] [Related]
14. Clinical implications of Parkinson's disease genetics.
Lorincz MT
Semin Neurol; 2006 Nov; 26(5):492-8. PubMed ID: 17048150
[TBL] [Abstract][Full Text] [Related]
15. Novel alpha-synuclein-immunoreactive proteins in brain samples from the Contursi kindred, Parkinson's, and Alzheimer's disease.
Langston JW; Sastry S; Chan P; Forno LS; Bolin LM; Di Monte DA
Exp Neurol; 1998 Dec; 154(2):684-90. PubMed ID: 9878203
[TBL] [Abstract][Full Text] [Related]
16. Large French-Canadian family with Lewy body parkinsonism: exclusion of known loci.
Grimes DA; Grimes JD; Racacho L; Scoggan KA; Han F; Schwarz BA; Woulfe J; Bulman D
Mov Disord; 2002 Nov; 17(6):1205-12. PubMed ID: 12465058
[TBL] [Abstract][Full Text] [Related]
17. Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.
Wszolek ZK; Gwinn-Hardy K; Wszolek EK; Muenter MD; Pfeiffer RF; Rodnitzky RL; Uitti RJ; McComb RD; Gasser T; Dickson DW
Acta Neuropathol; 2002 Apr; 103(4):344-50. PubMed ID: 11904753
[TBL] [Abstract][Full Text] [Related]
18. 5,10-methylenetetrahydrofolate reductase C677T gene polymorphism can influence age at onset of Parkinson's disease.
Lin JJ; Yueh KC; Liu CS; Liu JT; Lin SZ
Acta Neurol Taiwan; 2007 Sep; 16(3):150-7. PubMed ID: 17966954
[TBL] [Abstract][Full Text] [Related]
19. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
[TBL] [Abstract][Full Text] [Related]
20. Heredity in Parkinson's disease: new findings.
Lev N; Melamed E
Isr Med Assoc J; 2001 Jun; 3(6):435-8. PubMed ID: 11433638
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
