450 related articles for article (PubMed ID: 16983685)
1. 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. PubMed ID: 16983685
[TBL] [Abstract][Full Text] [Related]
2. Clinicopathologic correlation in PGRN mutations.
Davion S; Johnson N; Weintraub S; Mesulam MM; Engberg A; Mishra M; Baker M; Adamson J; Hutton M; Rademakers R; Bigio EH
Neurology; 2007 Sep; 69(11):1113-21. PubMed ID: 17522386
[TBL] [Abstract][Full Text] [Related]
3. Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.
Behrens MI; Mukherjee O; Tu PH; Liscic RM; Grinberg LT; Carter D; Paulsmeyer K; Taylor-Reinwald L; Gitcho M; Norton JB; Chakraverty S; Goate AM; Morris JC; Cairns NJ
Alzheimer Dis Assoc Disord; 2007; 21(1):1-7. PubMed ID: 17334266
[TBL] [Abstract][Full Text] [Related]
4. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Gass J; Cannon A; Mackenzie IR; Boeve B; Baker M; Adamson J; Crook R; Melquist S; Kuntz K; Petersen R; Josephs K; Pickering-Brown SM; Graff-Radford N; Uitti R; Dickson D; Wszolek Z; Gonzalez J; Beach TG; Bigio E; Johnson N; Weintraub S; Mesulam M; White CL; Woodruff B; Caselli R; Hsiung GY; Feldman H; Knopman D; Hutton M; Rademakers R
Hum Mol Genet; 2006 Oct; 15(20):2988-3001. PubMed ID: 16950801
[TBL] [Abstract][Full Text] [Related]
5. Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.
López de Munain A; Alzualde A; Gorostidi A; Otaegui D; Ruiz-Martínez J; Indakoetxea B; Ferrer I; Pérez-Tur J; Sáenz A; Bergareche A; Barandiarán M; Poza JJ; Zabalza R; Ruiz I; Urtasun M; Fernández-Manchola I; Olasagasti B; Espinal JB; Olaskoaga J; Ruibal M; Moreno F; Carrera N; Martí Massó JF
Biol Psychiatry; 2008 May; 63(10):946-52. PubMed ID: 17950702
[TBL] [Abstract][Full Text] [Related]
6. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Cruts M; Gijselinck I; van der Zee J; Engelborghs S; Wils H; Pirici D; Rademakers R; Vandenberghe R; Dermaut B; Martin JJ; van Duijn C; Peeters K; Sciot R; Santens P; De Pooter T; Mattheijssens M; Van den Broeck M; Cuijt I; Vennekens K; De Deyn PP; Kumar-Singh S; Van Broeckhoven C
Nature; 2006 Aug; 442(7105):920-4. PubMed ID: 16862115
[TBL] [Abstract][Full Text] [Related]
7. A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.
van der Zee J; Rademakers R; Engelborghs S; Gijselinck I; Bogaerts V; Vandenberghe R; Santens P; Caekebeke J; De Pooter T; Peeters K; Lübke U; Van den Broeck M; Martin JJ; Cruts M; De Deyn PP; Van Broeckhoven C; Dermaut B
Brain; 2006 Apr; 129(Pt 4):841-52. PubMed ID: 16495329
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 17003069
[TBL] [Abstract][Full Text] [Related]
9. Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.
Skoglund L; Brundin R; Olofsson T; Kalimo H; Ingvast S; Blom ES; Giedraitis V; Ingelsson M; Lannfelt L; Basun H; Glaser A
Neurogenetics; 2009 Feb; 10(1):27-34. PubMed ID: 18855025
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia.
Mukherjee O; Wang J; Gitcho M; Chakraverty S; Taylor-Reinwald L; Shears S; Kauwe JS; Norton J; Levitch D; Bigio EH; Hatanpaa KJ; White CL; Morris JC; Cairns NJ; Goate A
Hum Mutat; 2008 Apr; 29(4):512-21. PubMed ID: 18183624
[TBL] [Abstract][Full Text] [Related]
11. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.
Whitwell JL; Jack CR; Baker M; Rademakers R; Adamson J; Boeve BF; Knopman DS; Parisi JF; Petersen RC; Dickson DW; Hutton ML; Josephs KA
Arch Neurol; 2007 Mar; 64(3):371-6. PubMed ID: 17353379
[TBL] [Abstract][Full Text] [Related]
12. Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
Bronner IF; Rizzu P; Seelaar H; van Mil SE; Anar B; Azmani A; Donker Kaat L; Rosso S; Heutink P; van Swieten JC
Eur J Hum Genet; 2007 Mar; 15(3):369-74. PubMed ID: 17228326
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 17168647
[TBL] [Abstract][Full Text] [Related]
14. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
Josephs KA; Ahmed Z; Katsuse O; Parisi JF; Boeve BF; Knopman DS; Petersen RC; Davies P; Duara R; Graff-Radford NR; Uitti RJ; Rademakers R; Adamson J; Baker M; Hutton ML; Dickson DW
J Neuropathol Exp Neurol; 2007 Feb; 66(2):142-51. PubMed ID: 17278999
[TBL] [Abstract][Full Text] [Related]
15. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia.
van Swieten JC; Heutink P
Lancet Neurol; 2008 Oct; 7(10):965-74. PubMed ID: 18771956
[TBL] [Abstract][Full Text] [Related]
16. The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments.
Mackenzie IR; Rademakers R
Neurogenetics; 2007 Nov; 8(4):237-48. PubMed ID: 17805587
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 19101631
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 18192287
[TBL] [Abstract][Full Text] [Related]
19. Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.
Mishra M; Paunesku T; Woloschak GE; Siddique T; Zhu LJ; Lin S; Greco K; Bigio EH
Acta Neuropathol; 2007 Jul; 114(1):81-94. PubMed ID: 17569064
[TBL] [Abstract][Full Text] [Related]
20. Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.
Rosso SM; Kamphorst W; de Graaf B; Willemsen R; Ravid R; Niermeijer MF; Spillantini MG; Heutink P; van Swieten JC
Brain; 2001 Oct; 124(Pt 10):1948-57. PubMed ID: 11571213
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
