These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

471 related articles for article (PubMed ID: 17436289)

  • 1. Progranulin null mutations in both sporadic and familial frontotemporal dementia.
    Le Ber I; van der Zee J; Hannequin D; Gijselinck I; Campion D; Puel M; Laquerrière A; De Pooter T; Camuzat A; Van den Broeck M; Dubois B; Sellal F; Lacomblez L; Vercelletto M; Thomas-Antérion C; Michel BF; Golfier V; Didic M; Salachas F; Duyckaerts C; Cruts M; Verpillat P; Van Broeckhoven C; Brice A;
    Hum Mutat; 2007 Sep; 28(9):846-55. PubMed ID: 17436289
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
    Le Ber I; Camuzat A; Hannequin D; Pasquier F; Guedj E; Rovelet-Lecrux A; Hahn-Barma V; van der Zee J; Clot F; Bakchine S; Puel M; Ghanim M; Lacomblez L; Mikol J; Deramecourt V; Lejeune P; de la Sayette V; Belliard S; Vercelletto M; Meyrignac C; Van Broeckhoven C; Lambert JC; Verpillat P; Campion D; Habert MO; Dubois B; Brice A;
    Brain; 2008 Mar; 131(Pt 3):732-46. PubMed ID: 18245784
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
    van der Zee J; Le Ber I; Maurer-Stroh S; Engelborghs S; Gijselinck I; Camuzat A; Brouwers N; Vandenberghe R; Sleegers K; Hannequin D; Dermaut B; Schymkowitz J; Campion D; Santens P; Martin JJ; Lacomblez L; De Pooter T; Peeters K; Mattheijssens M; Vercelletto M; Van den Broeck M; Cruts M; De Deyn PP; Rousseau F; Brice A; Van Broeckhoven C
    Hum Mutat; 2007 Apr; 28(4):416. PubMed ID: 17345602
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distinct genetic forms of frontotemporal dementia.
    Seelaar H; Kamphorst W; Rosso SM; Azmani A; Masdjedi R; de Koning I; Maat-Kievit JA; Anar B; Donker Kaat L; Breedveld GJ; Dooijes D; Rozemuller JM; Bronner IF; Rizzu P; van Swieten JC
    Neurology; 2008 Oct; 71(16):1220-6. PubMed ID: 18703462
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progranulin locus deletion in frontotemporal dementia.
    Gijselinck I; van der Zee J; Engelborghs S; Goossens D; Peeters K; Mattheijssens M; Corsmit E; Del-Favero J; De Deyn PP; Van Broeckhoven C; Cruts M
    Hum Mutat; 2008 Jan; 29(1):53-8. PubMed ID: 18157829
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progranulin genetic variability contributes to amyotrophic lateral sclerosis.
    Sleegers K; Brouwers N; Maurer-Stroh S; van Es MA; Van Damme P; van Vught PW; van der Zee J; Serneels S; De Pooter T; Van den Broeck M; Cruts M; Schymkowitz J; De Jonghe P; Rousseau F; van den Berg LH; Robberecht W; Van Broeckhoven C
    Neurology; 2008 Jul; 71(4):253-9. PubMed ID: 18184915
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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. PubMed ID: 17923627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Clinical, pathological, and genetic characteristics of frontotemporal dementia and parkinsonism linked to chromosome 17 with mutations in the MAPT and PGRN].
    Tsuboi Y
    Brain Nerve; 2009 Nov; 61(11):1285-91. PubMed ID: 19938685
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.
    Ghidoni R; Benussi L; Glionna M; Franzoni M; Binetti G
    Neurology; 2008 Oct; 71(16):1235-9. PubMed ID: 18768919
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loss of progranulin function in frontotemporal lobar degeneration.
    Cruts M; Van Broeckhoven C
    Trends Genet; 2008 Apr; 24(4):186-94. PubMed ID: 18328591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases.
    Mackenzie IR; Feldman H
    Acta Neuropathol; 2003 Jun; 105(6):543-8. PubMed ID: 12734660
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
    Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
    Baker M; Mackenzie IR; Pickering-Brown SM; Gass J; Rademakers R; Lindholm C; Snowden J; Adamson J; Sadovnick AD; Rollinson S; Cannon A; Dwosh E; Neary D; Melquist S; Richardson A; Dickson D; Berger Z; Eriksen J; Robinson T; Zehr C; Dickey CA; Crook R; McGowan E; Mann D; Boeve B; Feldman H; Hutton M
    Nature; 2006 Aug; 442(7105):916-9. PubMed ID: 16862116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.