Payami H - Search Results

1

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.

2

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

3

Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.

Kay DM, Moran D, Moses L, Poorkaj P, Zabetian CP, Nutt J, Factor SA, Yu CE, Montimurro JS, Keefe RG, Schellenberg GD, Payami H. Kay DM, et al. Among authors: payami h. Ann Neurol. 2007 Jan;61(1):47-54. doi: 10.1002/ana.21039. Ann Neurol. 2007. PMID: 17187375

4

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

5

Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer disease.

Brickell KL, Steinbart EJ, Rumbaugh M, Payami H, Schellenberg GD, Van Deerlin V, Yuan W, Bird TD. Brickell KL, et al. Among authors: payami h. Arch Neurol. 2006 Sep;63(9):1307-11. doi: 10.1001/archneur.63.9.1307. Arch Neurol. 2006. PMID: 16966510

6

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.

Zabetian CP, Hutter CM, Factor SA, Nutt JG, Higgins DS, Griffith A, Roberts JW, Leis BC, Kay DM, Yearout D, Montimurro JS, Edwards KL, Samii A, Payami H. Zabetian CP, et al. Among authors: payami h. Ann Neurol. 2007 Aug;62(2):137-44. doi: 10.1002/ana.21157. Ann Neurol. 2007. PMID: 17514749 Free PMC article.

7

Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.

Hutter CM, Samii A, Factor SA, Nutt JG, Higgins DS, Bird TD, Griffith A, Roberts JW, Leis BC, Montimurro JS, Kay DM, Edwards KL, Payami H, Zabetian CP. Hutter CM, et al. Among authors: payami h. Eur J Neurol. 2008 Feb;15(2):134-9. doi: 10.1111/j.1468-1331.2007.02012.x. Epub 2007 Dec 18. Eur J Neurol. 2008. PMID: 18093156 Free PMC article.

8

Cognitive and motor function in long-duration PARKIN-associated Parkinson disease.

Alcalay RN, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Orbe Reilly M, Ruiz D, Louis ED, Comella CL, Nance MA, Bressman SB, Scott WK, Tanner CM, Mickel SF, Waters CH, Fahn S, Cote LJ, Frucht SJ, Ford B, Rezak M, Novak KE, Friedman JH, Pfeiffer RF, Marsh L, Hiner B, Payami H, Molho E, Factor SA, Nutt JG, Serrano C, Arroyo M, Ottman R, Pauciulo MW, Nichols WC, Clark LN, Marder KS. Alcalay RN, et al. Among authors: payami h. JAMA Neurol. 2014 Jan;71(1):62-7. doi: 10.1001/jamaneurol.2013.4498. JAMA Neurol. 2014. PMID: 24190026 Free PMC article.

9

Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.

Bird TD, Wijsman EM, Nochlin D, Leehey M, Sumi SM, Payami H, Poorkaj P, Nemens E, Rafkind M, Schellenberg GD. Bird TD, et al. Among authors: payami h. Neurology. 1997 Apr;48(4):949-54. doi: 10.1212/wnl.48.4.949. Neurology. 1997. PMID: 9109883

10

Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia.

Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, Tabira T, Trojanowski JQ, Borson S, Galasko D, Reich S, Quinn B, Schellenberg G, Bird TD. Poorkaj P, et al. Among authors: payami h. Arch Neurol. 2001 Mar;58(3):383-7. doi: 10.1001/archneur.58.3.383. Arch Neurol. 2001. PMID: 11255441

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