Similar articles for PMID: 9197268

Year	Number of Results
1977	1
1995	2
1996	1
1997	6
1998	26
1999	15
2000	11
2001	8
2002	9
2003	7
2004	12
2005	5
2009	1
2013	1
2014	1
2015	1
2024	0

1

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Polymeropoulos MH, et al. Science. 1997 Jun 27;276(5321):2045-7. doi: 10.1126/science.276.5321.2045. Science. 1997. PMID: 9197268

2

Autosomal dominant Parkinson's disease and alpha-synuclein.

Polymeropoulos MH. Polymeropoulos MH. Ann Neurol. 1998 Sep;44(3 Suppl 1):S63-4. doi: 10.1002/ana.410440710. Ann Neurol. 1998. PMID: 9749575 Review.

3

Genetics of Parkinson's disease.

Gasser T. Gasser T. Ann Neurol. 1998 Sep;44(3 Suppl 1):S53-7. doi: 10.1002/ana.410440708. Ann Neurol. 1998. PMID: 9749573 Review.

4

Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease.

Parsian A, Racette B, Zhang ZH, Chakraverty S, Rundle M, Goate A, Perlmutter JS. Parsian A, et al. Neurology. 1998 Dec;51(6):1757-9. doi: 10.1212/wnl.51.6.1757. Neurology. 1998. PMID: 9855543

5

The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom.

Warner TT, Schapira AH. Warner TT, et al. J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):378-9. doi: 10.1136/jnnp.65.3.378. J Neurol Neurosurg Psychiatry. 1998. PMID: 9728955 Free PMC article.

6

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.

Teive HA, Raskin S, Iwamoto FM, Germiniani FM, Baran MH, Werneck LC, Allan N, Quagliato E, Leroy E, Ide SE, Polymeropoulos MH. Teive HA, et al. Arq Neuropsiquiatr. 2001 Sep;59(3-B):722-4. doi: 10.1590/s0004-282x2001000500013. Arq Neuropsiquiatr. 2001. PMID: 11593272 Free article.

7

Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?

Papadimitriou A, Veletza V, Hadjigeorgiou GM, Patrikiou A, Hirano M, Anastasopoulos I. Papadimitriou A, et al. Neurology. 1999 Feb;52(3):651-4. doi: 10.1212/wnl.52.3.651. Neurology. 1999. PMID: 10025809

8

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.

Kobayashi H, Krüger R, Markopoulou K, Wszolek Z, Chase B, Taka H, Mineki R, Murayama K, Riess O, Mizuno Y, Hattori N. Kobayashi H, et al. Brain. 2003 Jan;126(Pt 1):32-42. doi: 10.1093/brain/awg010. Brain. 2003. PMID: 12477695

9

Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.

Papapetropoulos S, Ellul J, Paschalis C, Athanassiadou A, Papadimitriou A, Papapetropoulos T. Papapetropoulos S, et al. Eur J Neurol. 2003 May;10(3):281-6. doi: 10.1046/j.1468-1331.2003.00576.x. Eur J Neurol. 2003. PMID: 12752402

10

Failure to find the alpha-synuclein gene missense mutation (G209A) in 100 patients with younger onset Parkinson's disease.

Chan P, Tanner CM, Jiang X, Langston JW. Chan P, et al. Neurology. 1998 Feb;50(2):513-4. doi: 10.1212/wnl.50.2.513. Neurology. 1998. PMID: 9484385

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