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 *

251 related articles for article (PubMed ID: 18565828)

  • 1. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.
    Brouwers N; Sleegers K; Engelborghs S; Maurer-Stroh S; Gijselinck I; van der Zee J; Pickut BA; Van den Broeck M; Mattheijssens M; Peeters K; Schymkowitz J; Rousseau F; Martin JJ; Cruts M; De Deyn PP; Van Broeckhoven C
    Neurology; 2008 Aug; 71(9):656-64. PubMed ID: 18565828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Progranulin variability has no major role in Parkinson disease genetic etiology.
    Nuytemans K; Pals P; Sleegers K; Engelborghs S; Corsmit E; Peeters K; Pickut B; Mattheijssens M; Cras P; De Deyn PP; Theuns J; Van Broeckhoven C
    Neurology; 2008 Oct; 71(15):1147-51. PubMed ID: 18838661
    [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. Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
    Sleegers K; Brouwers N; Van Damme P; Engelborghs S; Gijselinck I; van der Zee J; Peeters K; Mattheijssens M; Cruts M; Vandenberghe R; De Deyn PP; Robberecht W; Van Broeckhoven C
    Ann Neurol; 2009 May; 65(5):603-9. PubMed ID: 19288468
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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. PubMed ID: 22647257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.
    Rovelet-Lecrux A; Deramecourt V; Legallic S; Maurage CA; Le Ber I; Brice A; Lambert JC; Frébourg T; Hannequin D; Pasquier F; Campion D
    Neurobiol Dis; 2008 Jul; 31(1):41-5. PubMed ID: 18479928
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update.
    Gijselinck I; Van Broeckhoven C; Cruts M
    Hum Mutat; 2008 Dec; 29(12):1373-86. PubMed ID: 18543312
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.
    Piaceri I; Pradella S; Cupidi C; Nannucci S; Polito C; Bagnoli S; Tedde A; Smirne N; Anfossi M; Gallo M; Bernardi L; Colao R; Maletta R; Bruni AC; Sorbi S; Nacmias B
    J Alzheimers Dis; 2014; 40(3):679-85. PubMed ID: 24503614
    [TBL] [Abstract][Full Text] [Related]  

  • 19. "Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation.
    Moreno F; Indakoetxea B; Barandiaran M; Alzualde A; Gabilondo A; Estanga A; Ruiz J; Ruibal M; Bergareche A; Martí-Massó JF; López de Munain A
    Neurology; 2009 Oct; 73(17):1367-74. PubMed ID: 19858458
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.