Parkinsonism and impulse control disorder: presentation of a new progranulin gene mutation
- PMID: 19133655
- DOI: 10.1002/mds.22429
Parkinsonism and impulse control disorder: presentation of a new progranulin gene mutation
Similar articles
-
Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.Mov Disord. 2017 Mar;32(3):476-478. doi: 10.1002/mds.26872. Epub 2016 Nov 15. Mov Disord. 2017. PMID: 27859661 No abstract available.
-
Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation.Parkinsonism Relat Disord. 2010 Aug;16(7):484-5. doi: 10.1016/j.parkreldis.2010.05.001. Epub 2010 Jun 8. Parkinsonism Relat Disord. 2010. PMID: 20570546 No abstract available.
-
Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.Arch Neurol. 2007 Jan;64(1):43-7. doi: 10.1001/archneur.64.1.43. Arch Neurol. 2007. PMID: 17210807
-
Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.Mov Disord. 2012 Jan;27(1):160-1. doi: 10.1002/mds.23956. Epub 2011 Sep 23. Mov Disord. 2012. PMID: 21953941 No abstract available.
-
Parkinsonism in Gaucher's disease type 1: ten new cases and a review of the literature.Mov Disord. 2009 Jul 30;24(10):1524-30. doi: 10.1002/mds.22593. Mov Disord. 2009. PMID: 19513999 Review.
Cited by
-
FTD-PSP is an Unusual Clinical Phenotype in A Frontotemporal Dementia Patient with A Novel Progranulin Mutation.Aging Dis. 2021 Oct 1;12(7):1741-1752. doi: 10.14336/AD.2021.0309. eCollection 2021 Oct. Aging Dis. 2021. PMID: 34631218 Free PMC article.
-
Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous