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P50 | author | Christine Van Broeckhoven | Q2247235 |
John Q. Trojanowski | Q6253636 | ||
Peter Riederer | Q7176599 | ||
Nenad Bogdanovic | Q96683791 | ||
Marc Cruts | Q114375600 | ||
Ainhoa Alzualde | Q114407906 | ||
Jill R Murrell | Q115633756 | ||
Rosa Rademakers | Q28777946 | ||
Jordan Grafman | Q30112579 | ||
Dennis W. Dickson | Q30504740 | ||
Marsel Mesulam | Q56862907 | ||
Bernardino F. Ghetti | Q56863342 | ||
Eileen H Bigio | Q57020324 | ||
Vivianna M Van Deerlin | Q59820064 | ||
Peter Paul De Deyn | Q60327954 | ||
Charles L White | Q60638965 | ||
William Hu | Q64605574 | ||
Peter Heutink | Q66718007 | ||
Murray Grossman | Q66724764 | ||
Marla Gearing | Q67212581 | ||
Thomas G Beach | Q67218653 | ||
Randall L Woltjer | Q67221637 | ||
Nigel J Cairns | Q67234695 | ||
Bradley F Boeve | Q67501037 | ||
Fermin Moreno | Q88264745 | ||
Alice S Chen-Plotkin | Q88981904 | ||
Patrick M Sleiman | Q90743109 | ||
Neill R Graff-Radford | Q91360658 | ||
Kimmo Hatanpaa | Q91409013 | ||
Gerard D Schellenberg | Q91709878 | ||
Albert Llado Plarrumani | Q91822909 | ||
Ronald L Hamilton | Q92023525 | ||
Harro Seelaar | Q92438245 | ||
Matthew Frosch | Q96050183 | ||
Myron F. Weiner | Q37370228 | ||
Jillian J. Kril | Q37840325 | ||
Jonathan D Rohrer | Q42407224 | ||
John Van Swieten | Q42684069 | ||
William S Brooks | Q43222873 | ||
Howard Feldman | Q44950327 | ||
Jeffrey Kaye | Q45263160 | ||
Glenda Halliday | Q45304807 | ||
Maria Martinez-Lage | Q45946614 | ||
Julie Snowden | Q50765521 | ||
Sebastiaan Engelborghs | Q56616406 | ||
Bruce L. Miller | Q56825815 | ||
P2093 | author name string | Robert Greene | |
Thomas D Bird | |||
Ian R A Mackenzie | |||
Salvatore Spina | |||
Virginia M Y Lee | |||
Elisabeth McCarty Wood | |||
Allison Goate | |||
Shaoxu Bing | |||
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions | Q30434949 | ||
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Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration | Q33978879 | ||
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Characteristics of frontotemporal dementia patients with a Progranulin mutation | Q34330746 | ||
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Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies | Q35607253 | ||
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Mutations in progranulin explain atypical phenotypes with variants in MAPT. | Q48384341 | ||
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene | Q48384348 | ||
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. | Q51970854 | ||
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. | Q51971909 | ||
Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations. | Q51972686 | ||
Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. | Q51973117 | ||
A novel deletion in progranulin gene is associated with FTDP-17 and CBS. | Q53509247 | ||
P433 | issue | 4 | |
P921 | main subject | frontotemporal lobar degeneration | Q18579 |
P304 | page(s) | 488-497 | |
P577 | publication date | 2011-04-01 | |
P1433 | published in | Archives of Neurology | Q15766672 |
P1476 | title | Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration | |
P478 | volume | 68 |
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