Momeni P - Search Results

1

Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia.

Momeni P, Wickremaratchi MM, Bell J, Arnold R, Beer R, Hardy J, Revesz T, Neal JW, Morris HR. Momeni P, et al. Clin Neurol Neurosurg. 2010 Dec;112(10):917-20. doi: 10.1016/j.clineuro.2010.07.015. Epub 2010 Aug 12. Clin Neurol Neurosurg. 2010. PMID: 20708332

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 presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease.

Edwards-Lee T, Wen J, Bell J, Hardy J, Chung J, Momeni P. Edwards-Lee T, et al. Among authors: momeni p. Neurosci Lett. 2006 May 8;398(3):251-2. doi: 10.1016/j.neulet.2006.01.006. Epub 2006 Feb 15. Neurosci Lett. 2006. PMID: 16469444

5

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

6

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.

7

Genetic variability in CHMP2B and frontotemporal dementia.

Momeni P, Rogaeva E, Van Deerlin V, Yuan W, Grafman J, Tierney M, Huey E, Bell J, Morris CM, Kalaria RN, van Rensburg SJ, Niehaus D, Potocnik F, Kawarai T, Salehi-Rad S, Sato C, St George-Hyslop P, Hardy J. Momeni P, et al. Neurodegener Dis. 2006;3(3):129-33. doi: 10.1159/000094771. Neurodegener Dis. 2006. PMID: 16954699

8

Characteristics of frontotemporal dementia patients with a Progranulin mutation.

Huey ED, Grafman J, Wassermann EM, Pietrini P, Tierney MC, Ghetti B, Spina S, Baker M, Hutton M, Elder JW, Berger SL, Heflin KA, Hardy J, Momeni P. Huey ED, et al. Among authors: momeni p. Ann Neurol. 2006 Sep;60(3):374-80. doi: 10.1002/ana.20969. Ann Neurol. 2006. PMID: 16983677 Free PMC article.

9

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

Masellis M, Momeni P, Meschino W, Heffner R Jr, Elder J, Sato C, Liang Y, St George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E. Masellis M, et al. Among authors: momeni p. Brain. 2006 Nov;129(Pt 11):3115-23. doi: 10.1093/brain/awl276. Epub 2006 Oct 9. Brain. 2006. PMID: 17030534

10

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

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