Payami H - Search Results

1

Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysis.

Factor SA, Steenland NK, Higgins DS, Molho ES, Kay DM, Montimurro J, Rosen AR, Zabetian CP, Payami H. Factor SA, et al. Among authors: payami h. J Neurol Neurosurg Psychiatry. 2011 May;82(5):564-8. doi: 10.1136/jnnp.2010.222042. Epub 2010 Sep 30. J Neurol Neurosurg Psychiatry. 2011. PMID: 20884673 Free PMC article.

2

Parkinson's disease, CYP2D6 polymorphism, and age.

Payami H, Lee N, Zareparsi S, Gonzales McNeal M, Camicioli R, Bird TD, Sexton G, Gancher S, Kaye J, Calhoun D, Swanson PD, Nutt J. Payami H, et al. Neurology. 2001 May 22;56(10):1363-70. doi: 10.1212/wnl.56.10.1363. Neurology. 2001. PMID: 11376189

3

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.

4

False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy.

Factor SA, Qian J, Lava NS, Hubbard JD, Payami H. Factor SA, et al. Among authors: payami h. Ann Neurol. 2005 Mar;57(3):462-3. doi: 10.1002/ana.20389. Ann Neurol. 2005. PMID: 15732096 No abstract available.

5

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.

6

One step closer to fixing association studies: evidence for age- and gender-specific allele frequency variations and deviations from Hardy-Weinberg expectations in controls.

Payami H, Zhu M, Montimurro J, Keefe R, McCulloch CC, Moses L. Payami H, et al. Hum Genet. 2005 Dec;118(3-4):322-30. doi: 10.1007/s00439-005-0057-1. Epub 2005 Sep 28. Hum Genet. 2005. PMID: 16189709

7

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.

Kay DM, Zabetian CP, Factor SA, Nutt JG, Samii A, Griffith A, Bird TD, Kramer P, Higgins DS, Payami H. Kay DM, et al. Among authors: payami h. Mov Disord. 2006 Apr;21(4):519-23. doi: 10.1002/mds.20751. Mov Disord. 2006. PMID: 16250030

8

Analysis of the LRRK2 G2019S mutation in Alzheimer Disease.

Zabetian CP, Lauricella CJ, Tsuang DW, Leverenz JB, Schellenberg GD, Payami H. Zabetian CP, et al. Among authors: payami h. Arch Neurol. 2006 Jan;63(1):156-7. doi: 10.1001/archneur.63.1.156. Arch Neurol. 2006. PMID: 16401756 Free PMC article. No abstract available.

9

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, Leis BC, Bird TD, Nutt JG, Higgins DS, Roberts JW, Kay DM, Edwards KL, Samii A, Payami H. Zabetian CP, et al. Among authors: payami h. Am J Hum Genet. 2006 Oct;79(4):752-8. doi: 10.1086/508025. Epub 2006 Aug 17. Am J Hum Genet. 2006. PMID: 16960813 Free PMC article.

10

Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease.

Kay DM, Bird TD, Zabetian CP, Factor SA, Samii A, Higgins DS, Nutt J, Roberts JW, Griffith A, Leis BC, Montimurro JS, Philpott S, Payami H. Kay DM, et al. Among authors: payami h. Genet Test. 2006 Fall;10(3):221-7. doi: 10.1089/gte.2006.10.221. Genet Test. 2006. PMID: 17020475

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