198 related articles for article (PubMed ID: 17353379)
1. 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]
2. 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]
3. 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]
4. Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.
Whitwell JL; Jack CR; Boeve BF; Senjem ML; Baker M; Rademakers R; Ivnik RJ; Knopman DS; Wszolek ZK; Petersen RC; Josephs KA
Neurology; 2009 Mar; 72(9):813-20. PubMed ID: 19255408
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 18593276
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Frontotemporal lobar degeneration without lobar atrophy.
Josephs KA; Whitwell JL; Jack CR; Parisi JE; Dickson DW
Arch Neurol; 2006 Nov; 63(11):1632-8. PubMed ID: 17101834
[TBL] [Abstract][Full Text] [Related]
10. Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.
van der Zee J; Gijselinck I; Pirici D; Kumar-Singh S; Cruts M; Van Broeckhoven C
Neurodegener Dis; 2007; 4(2-3):227-35. PubMed ID: 17596717
[TBL] [Abstract][Full Text] [Related]
11. TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions.
Neumann M; Kwong LK; Truax AC; Vanmassenhove B; Kretzschmar HA; Van Deerlin VM; Clark CM; Grossman M; Miller BL; Trojanowski JQ; Lee VM
J Neuropathol Exp Neurol; 2007 Mar; 66(3):177-83. PubMed ID: 17356379
[TBL] [Abstract][Full Text] [Related]
12. The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.
Mackenzie IR; Baker M; Pickering-Brown S; Hsiung GY; Lindholm C; Dwosh E; Gass J; Cannon A; Rademakers R; Hutton M; Feldman HH
Brain; 2006 Nov; 129(Pt 11):3081-90. PubMed ID: 17071926
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
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. PubMed ID: 17003069
[TBL] [Abstract][Full Text] [Related]
16. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
Neumann M; Mackenzie IR; Cairns NJ; Boyer PJ; Markesbery WR; Smith CD; Taylor JP; Kretzschmar HA; Kimonis VE; Forman MS
J Neuropathol Exp Neurol; 2007 Feb; 66(2):152-7. PubMed ID: 17279000
[TBL] [Abstract][Full Text] [Related]
17. Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.
Boeve BF; Baker M; Dickson DW; Parisi JE; Giannini C; Josephs KA; Hutton M; Pickering-Brown SM; Rademakers R; Tang-Wai D; Jack CR; Kantarci K; Shiung MM; Golde T; Smith GE; Geda YE; Knopman DS; Petersen RC
Brain; 2006 Nov; 129(Pt 11):3103-14. PubMed ID: 17030535
[TBL] [Abstract][Full Text] [Related]
18. Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.
Spina S; Murrell JR; Huey ED; Wassermann EM; Pietrini P; Baraibar MA; Barbeito AG; Troncoso JC; Vidal R; Ghetti B; Grafman J
Neurology; 2007 Mar; 68(11):820-7. PubMed ID: 17202431
[TBL] [Abstract][Full Text] [Related]
19. Progranulin gene mutation with an unusual clinical and neuropathologic presentation.
Wider C; Uitti RJ; Wszolek ZK; Fang JY; Josephs KA; Baker MC; Rademakers R; Hutton ML; Dickson DW
Mov Disord; 2008 Jun; 23(8):1168-73. PubMed ID: 18442119
[TBL] [Abstract][Full Text] [Related]
20. Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.
Van Deerlin VM; Wood EM; Moore P; Yuan W; Forman MS; Clark CM; Neumann M; Kwong LK; Trojanowski JQ; Lee VM; Grossman M
Arch Neurol; 2007 Aug; 64(8):1148-53. PubMed ID: 17698705
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]