Momeni P - Search Results

1

Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis.

Ferrari R, Forabosco P, Vandrovcova J, Botía JA, Guelfi S, Warren JD; UK Brain Expression Consortium (UKBEC); Momeni P, Weale ME, Ryten M, Hardy J. Ferrari R, et al. Among authors: momeni p. Mol Neurodegener. 2016 Feb 24;11:21. doi: 10.1186/s13024-016-0085-4. Mol Neurodegener. 2016. PMID: 26912063 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

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

4

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.

5

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

6

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.

7

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

8

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

9

Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.

Bruni AC, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, Kawarai T, Sato C, Pradella S, Wakutani Y, Anfossi M, Gallo M, Geracitano S, Costanzo A, Smirne N, Curcio SA, Mirabelli M, Puccio G, Colao R, Maletta RG, Kertesz A, St George-Hyslop P, Hardy J, Rogaeva E. Bruni AC, et al. Among authors: momeni p. Neurology. 2007 Jul 10;69(2):140-7. doi: 10.1212/01.wnl.0000265220.64396.b4. Neurology. 2007. PMID: 17620546

10

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.

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