Momeni P - Search Results

1

Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.

Ferrari R, Ryten M, Simone R, Trabzuni D, Nicolaou N, Hondhamuni G, Ramasamy A, Vandrovcova J; UK Brain Expression Consortium; Weale ME, Lees AJ, Momeni P, Hardy J, de Silva R. Ferrari R, et al. Among authors: momeni p. Neurobiol Aging. 2014 Jun;35(6):1514.e1-12. doi: 10.1016/j.neurobiolaging.2014.01.010. Epub 2014 Jan 13. Neurobiol Aging. 2014. PMID: 24503276 Free PMC article.

2

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

Momeni P, Cairns NJ, Perry RH, Bigio EH, Gearing M, Singleton AB, Hardy J. Momeni P, et al. Neurobiol Aging. 2006 May;27(5):778.e1-778.e6. doi: 10.1016/j.neurobiolaging.2005.03.030. Epub 2005 Jul 7. Neurobiol Aging. 2006. PMID: 16005115

3

Taiwanese cases of SCA2 are derived from a single founder.

Momeni P, Lu CS, Chou YH, Chang HC, Chen RS, Chen CC, Hsu JT, Singleton A, Hardy J. Momeni P, et al. Mov Disord. 2005 Dec;20(12):1633-6. doi: 10.1002/mds.20638. Mov Disord. 2005. PMID: 16078202

4

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia.

Malkani R, D'Souza I, Gwinn-Hardy K, Schellenberg GD, Hardy J, Momeni P. Malkani R, et al. Among authors: momeni p. Neurobiol Dis. 2006 May;22(2):401-3. doi: 10.1016/j.nbd.2005.12.001. Epub 2006 Feb 28. Neurobiol Dis. 2006. PMID: 16503405

5

Frontal temporal dementia: dissecting the aetiology and pathogenesis.

Hardy J, Momeni P, Traynor BJ. Hardy J, et al. Among authors: momeni p. Brain. 2006 Apr;129(Pt 4):830-1. doi: 10.1093/brain/awl035. Brain. 2006. PMID: 16543401 No abstract available.

6

Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B.

Momeni P, Bell J, Duckworth J, Hutton M, Mann D, Brown SP, Hardy J. Momeni P, et al. Neurosci Lett. 2006 Dec 20;410(2):77-9. doi: 10.1016/j.neulet.2006.06.065. Neurosci Lett. 2006. PMID: 17095158

7

Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation.

Momeni P, Pittman A, Lashley T, Vandrovcova J, Malzer E, Luk C, Hulette C, Lees A, Revesz T, Hardy J, de Silva R. Momeni P, et al. Neurobiol Aging. 2009 Mar;30(3):388-93. doi: 10.1016/j.neurobiolaging.2007.07.013. Epub 2007 Aug 27. Neurobiol Aging. 2009. PMID: 17723255 Free PMC article.

8

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.

Camargos ST, Dornas LO, Momeni P, Lees A, Hardy J, Singleton A, Cardoso F. Camargos ST, et al. Among authors: momeni p. Mov Disord. 2009 Apr 15;24(5):662-6. doi: 10.1002/mds.22365. Mov Disord. 2009. PMID: 19205068 Free PMC article.

9

Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia.

Momeni P, DeTucci K, Straub RE, Weinberger DR, Davies P, Grafman J, Hardy J, Huey ED. Momeni P, et al. Neurocase. 2010 Jun;16(3):273-9. doi: 10.1080/13554790903456209. Epub 2010 Jan 18. Neurocase. 2010. PMID: 20087814 Free PMC article.

10

Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementia.

Ferrari R, Kapogiannis D, Huey ED, Grafman J, Hardy J, Momeni P. Ferrari R, et al. Among authors: momeni p. Alzheimer Dis Assoc Disord. 2010 Oct-Dec;24(4):397-401. doi: 10.1097/WAD.0b013e3181df20c7. Alzheimer Dis Assoc Disord. 2010. PMID: 20592581 Free PMC article.

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