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Items: 1 to 20 of 67

1.

Locus-specific mutation databases for neurodegenerative brain diseases.

Cruts M, Theuns J, Van Broeckhoven C.

Hum Mutat. 2012 Sep;33(9):1340-4. doi: 10.1002/humu.22117. Epub 2012 Jul 2.

2.

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K.

Arch Neurol. 2007 Oct;64(10):1436-46.

PMID:
17923627
3.

Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: detection of GRN mutations in a Spanish cohort.

Antonell A, Gil S, Sánchez-Valle R, Balasa M, Bosch B, Prat MC, Chiollaz AC, Fernández M, Yagüe J, Molinuevo JL, Lladó A.

J Alzheimers Dis. 2012;31(3):581-91. doi: 10.3233/JAD-2012-112120.

PMID:
22647257
4.

CHMP2B mutations are rare in French families with frontotemporal lobar degeneration.

Ghanim M, Guillot-Noel L, Pasquier F, Jornea L, Deramecourt V, Dubois B, Le Ber I, Brice A; French Research Network on FTD and FTD/MND.

J Neurol. 2010 Dec;257(12):2032-6. doi: 10.1007/s00415-010-5655-8. Epub 2010 Jul 14.

PMID:
20625756
5.

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Gijselinck I, Engelborghs S, Maes G, Cuijt I, Peeters K, Mattheijssens M, Joris G, Cras P, Martin JJ, De Deyn PP, Kumar-Singh S, Van Broeckhoven C, Cruts M.

Arch Neurol. 2010 May;67(5):606-16. doi: 10.1001/archneurol.2010.82.

PMID:
20457961
6.

Invited article: the Alzheimer disease-frontotemporal lobar degeneration spectrum.

van der Zee J, Sleegers K, Van Broeckhoven C.

Neurology. 2008 Oct 7;71(15):1191-7. doi: 10.1212/01.wnl.0000327523.52537.86. Review.

PMID:
18838666
7.

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration.

Lladó A, Sánchez-Valle R, Rey MJ, Ezquerra M, Tolosa E, Ferrer I, Molinuevo JL; Catalan collaborative Study Group for FTLD.

J Neurol. 2008 Apr;255(4):488-94. doi: 10.1007/s00415-008-0565-8. Epub 2008 Mar 25.

PMID:
18357425
8.

In search of genes involved in neurodegenerative disorders.

Pardo LM, van Duijn CM.

Mutat Res. 2005 Dec 30;592(1-2):89-101. Epub 2005 Jul 11. Review.

PMID:
16009383
9.

Role of progranulin as a biomarker for Alzheimer's disease.

Sleegers K, Brouwers N, Van Broeckhoven C.

Biomark Med. 2010 Feb;4(1):37-50. Review.

PMID:
20387302
10.

Prevalence of frontotemporal lobar degeneration in an isolated population: the Vallecamonica study.

Gilberti N, Turla M, Alberici A, Bertasi V, Civelli P, Archetti S, Padovani A, Borroni B.

Neurol Sci. 2012 Aug;33(4):899-904. doi: 10.1007/s10072-011-0865-0. Epub 2011 Nov 30.

PMID:
22127750
11.

Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.

Krüger J, Moilanen V, Majamaa K, Remes AM.

Alzheimer Dis Assoc Disord. 2012 Jul-Sep;26(3):272-6. doi: 10.1097/WAD.0b013e318231e6c7.

PMID:
21959359
12.

Towards unveiling the genetics of neurodegenerative diseases.

Lill CM, Bertram L.

Semin Neurol. 2011 Nov;31(5):531-41. doi: 10.1055/s-0031-1299791. Epub 2012 Jan 21. Review.

PMID:
22266890
13.
14.

Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis.

Chen Y, Li S, Su L, Sheng J, Lv W, Chen G, Xu Z.

J Neurol. 2015;262(4):814-22. doi: 10.1007/s00415-014-7630-2. Epub 2015 Jan 13.

PMID:
25578179
15.

Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy.

Bagnoli S, Piaceri I, Tedde A, Piacentini S, Nannucci S, Bracco L, Sorbi S, Nacmias B.

Cell Mol Neurobiol. 2012 Jan;32(1):13-6. doi: 10.1007/s10571-011-9741-y. Epub 2011 Jul 29.

PMID:
21800185
16.

Genetic contributors to frontotemporal lobar degeneration: beyond monogenic disease.

Borroni B, Pilotto A, Bianchi M, Gilberti N, Padovani A.

Mini Rev Med Chem. 2011 Oct;11(11):988-1001. Review.

PMID:
21762097
17.

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

Benussi L, Ghidoni R, Pegoiani E, Moretti DV, Zanetti O, Binetti G.

Neurobiol Dis. 2009 Mar;33(3):379-85. doi: 10.1016/j.nbd.2008.11.008. Epub 2008 Dec 6.

PMID:
19101631
18.

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

Cerami C, Marcone A, Galimberti D, Villa C, Scarpini E, Cappa SF.

J Alzheimers Dis. 2011;27(4):791-7. doi: 10.3233/JAD-2011-110788.

PMID:
21891869
19.

[Frontotemporal lobar degeneration: a diagnostic challenge].

Remes AM.

Duodecim. 2010;126(18):2189-95. Review. Finnish.

PMID:
21072965
20.

[Advances in biological psychiatry research on dementia: AD-FTLD spectrum].

Takeda M.

Brain Nerve. 2012 Feb;64(2):149-61. Review. Japanese.

PMID:
22308260

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