Payami H - Search Results

1

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

Hamza TH, Zabetian CP, Tenesa A, Laederach A, Montimurro J, Yearout D, Kay DM, Doheny KF, Paschall J, Pugh E, Kusel VI, Collura R, Roberts J, Griffith A, Samii A, Scott WK, Nutt J, Factor SA, Payami H. Hamza TH, et al. Among authors: payami h. Nat Genet. 2010 Sep;42(9):781-5. doi: 10.1038/ng.642. Epub 2010 Aug 15. Nat Genet. 2010. PMID: 20711177 Free PMC article.

2

Increased risk of Parkinson's disease in parents and siblings of patients.

Payami H, Larsen K, Bernard S, Nutt J. Payami H, et al. Ann Neurol. 1994 Oct;36(4):659-61. doi: 10.1002/ana.410360417. Ann Neurol. 1994. PMID: 7605419

3

Genetic anticipation in Parkinson's disease.

Payami H, Bernard S, Larsen K, Kaye J, Nutt J. Payami H, et al. Neurology. 1995 Jan;45(1):135-8. doi: 10.1212/wnl.45.1.135. Neurology. 1995. PMID: 7824103 Clinical Trial.

4

Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease.

Zareparsi S, Kaye J, Camicioli R, Kramer P, Nutt J, Bird T, Litt M, Payami H. Zareparsi S, et al. Among authors: payami h. Lancet. 1998 Jan 3;351(9095):37-8. doi: 10.1016/s0140-6736(05)78089-2. Lancet. 1998. PMID: 9433434 No abstract available.

5

Exclusion of dominant mutations within the FTDP-17 locus on chromosome 17 for Parkinson's disease.

Zareparsi S, Wirdefeldt K, Burgess CE, Nutt J, Kramer P, Schalling M, Payami H. Zareparsi S, et al. Among authors: payami h. Neurosci Lett. 1999 Sep 10;272(2):140-2. doi: 10.1016/s0304-3940(99)00581-9. Neurosci Lett. 1999. PMID: 10507561

6

Age at onset of Parkinson disease and apolipoprotein E genotypes.

Zareparsi S, Camicioli R, Sexton G, Bird T, Swanson P, Kaye J, Nutt J, Payami H. Zareparsi S, et al. Among authors: payami h. Am J Med Genet. 2002 Jan 15;107(2):156-61. doi: 10.1002/ajmg.10111. Am J Med Genet. 2002. PMID: 11807891

7

Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease.

Payami H, Zareparsi S, James D, Nutt J. Payami H, et al. Arch Neurol. 2002 May;59(5):848-50. doi: 10.1001/archneur.59.5.848. Arch Neurol. 2002. PMID: 12020270

8

parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.

Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H. Poorkaj P, et al. Among authors: payami h. Am J Med Genet A. 2004 Aug 15;129A(1):44-50. doi: 10.1002/ajmg.a.30157. Am J Med Genet A. 2004. PMID: 15266615

9

Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.

Poorkaj P, Moses L, Montimurro JS, Nutt JG, Schellenberg GD, Payami H. Poorkaj P, et al. Among authors: payami h. BMC Neurol. 2005 Feb 22;5(1):4. doi: 10.1186/1471-2377-5-4. BMC Neurol. 2005. PMID: 15725358 Free PMC article.

10

Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation.

Kay DM, Kramer P, Higgins D, Zabetian CP, Payami H. Kay DM, et al. Among authors: payami h. Mov Disord. 2005 Aug;20(8):1077-8. doi: 10.1002/mds.20618. Mov Disord. 2005. PMID: 16001413 No abstract available.

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