Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 5

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.

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
3.

Intrafamilial clinical phenotypic heterogeneity with progranulin gene p.Glu498fs mutation.

Larner AJ.

J Neurol Sci. 2012 May 15;316(1-2):189-90. doi: 10.1016/j.jns.2012.01.005. Epub 2012 Jan 26. Review.

PMID:
22280948
4.

Chromosome 17 in FTLD: from MAPT tau to progranulin and back.

Alberici A, Cosseddu M, Padovani A, Borroni B.

Curr Alzheimer Res. 2011 May;8(3):229-36. Review.

PMID:
21222603
5.

Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Kumar-Singh S, Van Broeckhoven C.

Curr Alzheimer Res. 2006 Dec;3(5):485-91. Review.

PMID:
17168647

Supplemental Content

Support Center