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Results: 1 to 20 of 100

Related Citations for PubMed (Select 22491866)

1.

Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin.

McDade E, Boeve BF, Burrus TM, Boot BP, Kantarci K, Fields J, Lowe VJ, Peller P, Knopman D, Baker M, Finch N, Rademakers R, Petersen R.

Neurology. 2012 Apr 17;78(16):1245-9. doi: 10.1212/WNL.0b013e318251594c. Epub 2012 Apr 4.

2.

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.

Ann Neurol. 2006 Sep;60(3):374-80.

3.

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

Gabryelewicz T, Masellis M, Berdynski M, Bilbao JM, Rogaeva E, St George-Hyslop P, Barczak A, Czyzewski K, Barcikowska M, Wszolek Z, Black SE, Zekanowski C.

J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413.

PMID:
20930269
4.

Corticobasal syndrome associated with the A9D Progranulin mutation.

Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Grafman J, Ghetti B.

J Neuropathol Exp Neurol. 2007 Oct;66(10):892-900.

PMID:
17917583
5.

Early signs of VCP-related frontotemporal dementia: a neuropsychological, FDG-PET and fMRI study.

Kalbe E, Onur OA, Minnerop M, Reimann J, Althaus A, Ahmadzadehfar H, Dodel R, Strach K, Clemen CS, Herholz K, Haense C, Fink GR, Schröder R.

J Neurol. 2011 Mar;258(3):515-8. doi: 10.1007/s00415-010-5774-2. Epub 2010 Oct 12. Review. No abstract available.

PMID:
20938780
6.

Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.

Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC.

Neurobiol Aging. 2009 Nov;30(11):1825-33. doi: 10.1016/j.neurobiolaging.2008.01.005. Epub 2008 Mar 7.

PMID:
18314228
7.

Low serum progranulin predicts the presence of mutations: a prospective study.

Schofield EC, Halliday GM, Kwok J, Loy C, Double KL, Hodges JR.

J Alzheimers Dis. 2010;22(3):981-4. doi: 10.3233/JAD-2010-101032.

PMID:
20858962
8.

Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.

Barandiaran M, Estanga A, Moreno F, Indakoetxea B, Alzualde A, Balluerka N, Martí Massó JF, López de Munain A.

J Int Neuropsychol Soc. 2012 Nov;18(6):1086-90. doi: 10.1017/S1355617712000823.

PMID:
23158232
9.

Progranulin peripheral levels as a screening tool for the identification of subjects with progranulin mutations in a Portuguese cohort.

Almeida MR, Baldeiras I, Ribeiro MH, Santiago B, Machado C, Massano J, Guimarães J, Resende Oliveira C, Santana I.

Neurodegener Dis. 2014;13(4):214-23. doi: 10.1159/000352022. Epub 2013 Sep 6.

PMID:
24022032
10.

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.

Kelley BJ, Haidar W, Boeve BF, Baker M, Shiung M, Knopman DS, Rademakers R, Hutton M, Adamson J, Kuntz KM, Dickson DW, Parisi JE, Smith GE, Petersen RC.

Arch Neurol. 2010 Feb;67(2):171-7. doi: 10.1001/archneurol.2010.113.

11.
12.

Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia.

Passov V, Gavrilova RH, Strand E, Cerhan JH, Josephs KA.

Arch Neurol. 2011 Mar;68(3):376-80. doi: 10.1001/archneurol.2011.26.

PMID:
21403024
13.

Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series.

Borroni B, Archetti S, Alberici A, Agosti C, Gennarelli M, Bigni B, Bonvicini C, Ferrari M, Bellelli G, Galimberti D, Scarpini E, Di Lorenzo D, Caimi L, Caltagirone C, Di Luca M, Padovani A.

Neurogenetics. 2008 Jul;9(3):197-205. doi: 10.1007/s10048-008-0127-3. Epub 2008 Apr 8.

PMID:
18392865
14.

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.

Pickering-Brown SM, Rollinson S, Du Plessis D, Morrison KE, Varma A, Richardson AM, Neary D, Snowden JS, Mann DM.

Brain. 2008 Mar;131(Pt 3):721-31. doi: 10.1093/brain/awm331. Epub 2008 Jan 11.

15.

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia.

Snowden JS, Pickering-Brown SM, Mackenzie IR, Richardson AM, Varma A, Neary D, Mann DM.

Brain. 2006 Nov;129(Pt 11):3091-102. Epub 2006 Sep 26.

16.

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin.

Mukherjee O, Pastor P, Cairns NJ, Chakraverty S, Kauwe JS, Shears S, Behrens MI, Budde J, Hinrichs AL, Norton J, Levitch D, Taylor-Reinwald L, Gitcho M, Tu PH, Tenenholz Grinberg L, Liscic RM, Armendariz J, Morris JC, Goate AM.

Ann Neurol. 2006 Sep;60(3):314-22.

17.

Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.

Pietroboni AM, Fumagalli GG, Ghezzi L, Fenoglio C, Cortini F, Serpente M, Cantoni C, Rotondo E, Corti P, Carecchio M, Bassi M, Bresolin N, Galbiati D, Galimberti D, Scarpini E.

J Alzheimers Dis. 2011;24(2):253-9. doi: 10.3233/JAD-2011-101704.

PMID:
21258152
18.

Cerebral metabolism, anatomy, and cognition in monozygotic twins discordant for dementia of the Alzheimer type.

Luxenberg JS, May C, Haxby JV, Grady C, Moore A, Berg G, White BJ, Robinette D, Rapoport SI.

J Neurol Neurosurg Psychiatry. 1987 Mar;50(3):333-40.

19.

Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers.

Borroni B, Alberici A, Premi E, Archetti S, Garibotto V, Agosti C, Gasparotti R, Di Luca M, Perani D, Padovani A.

Rejuvenation Res. 2008 Jun;11(3):585-95. doi: 10.1089/rej.2007.0623.

PMID:
18593276
20.

Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autism.

Kates WR, Burnette CP, Eliez S, Strunge LA, Kaplan D, Landa R, Reiss AL, Pearlson GD.

Am J Psychiatry. 2004 Mar;161(3):539-46.

PMID:
14992981
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