BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

84 related articles for article (PubMed ID: 22336192)

  • 1. Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population.
    Verstraeten A; Wauters E; Crosiers D; Meeus B; Corsmit E; Elinck E; Mattheijssens M; Peeters K; Cras P; Pickut B; Vandenberghe R; Engelborghs S; De Deyn PP; Van Broeckhoven C; Theuns J
    Neurobiol Aging; 2012 Aug; 33(8):1844.e11-3. PubMed ID: 22336192
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DLB and PDD: a role for mutations in dementia and Parkinson disease genes?
    Meeus B; Verstraeten A; Crosiers D; Engelborghs S; Van den Broeck M; Mattheijssens M; Peeters K; Corsmit E; Elinck E; Pickut B; Vandenberghe R; Cras P; De Deyn PP; Van Broeckhoven C; Theuns J
    Neurobiol Aging; 2012 Mar; 33(3):629.e5-629.e18. PubMed ID: 22118943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Family history of dementia is a risk factor for Lewy body disease.
    Woodruff BK; Graff-Radford NR; Ferman TJ; Dickson DW; DeLucia MW; Crook JE; Arvanitakis Z; Brassler S; Waters C; Barker W; Duara R
    Neurology; 2006 Jun; 66(12):1949-50. PubMed ID: 16801670
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of VPS35 mutations replicated in French families with Parkinson disease.
    Lesage S; Condroyer C; Klebe S; Honoré A; Tison F; Brefel-Courbon C; Dürr A; Brice A;
    Neurology; 2012 May; 78(18):1449-50. PubMed ID: 22517097
    [No Abstract]   [Full Text] [Related]  

  • 5. Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease.
    Zhang Y; Chen S; Xiao Q; Cao L; Liu J; Rong TY; Ma JF; Wang G; Wang Y; Chen SD
    Parkinsonism Relat Disord; 2012 Jun; 18(5):638-40. PubMed ID: 22410496
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
    van Blitterswijk M; Blokhuis A; van Es MA; van Vught PW; Rowicka PA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
    Neurobiol Aging; 2012 Aug; 33(8):1845.e1-3. PubMed ID: 22330174
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.
    Zheng K; Heydari B; Simon DK
    Arch Neurol; 2003 May; 60(5):722-5. PubMed ID: 12756136
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A single-nucleotide polymorphism of the osteopontin gene may contribute to a susceptibility to Lewy body disease.
    Maetzler W; Michelis J; Tomiuk J; Melms A; Becker C; Gasser T; Schulte C; Berg D
    J Neural Transm (Vienna); 2009 May; 116(5):599-605. PubMed ID: 19340392
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.
    Groen EJ; van Rheenen W; Koppers M; van Doormaal PT; Vlam L; Diekstra FP; Dooijes D; Pasterkamp RJ; van den Berg LH; Veldink JH
    Neurobiol Aging; 2012 Aug; 33(8):1852.e1-3. PubMed ID: 22507827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic variability of the retromer cargo recognition complex in parkinsonism.
    Gustavsson EK; Guella I; Trinh J; Szu-Tu C; Rajput A; Rajput AH; Steele JC; McKeown M; Jeon BS; Aasly JO; Farrer MJ
    Mov Disord; 2015 Apr; 30(4):580-4. PubMed ID: 25475142
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
    Ogaki K; Koga S; Heckman MG; Fiesel FC; Ando M; Labbé C; Lorenzo-Betancor O; Moussaud-Lamodière EL; Soto-Ortolaza AI; Walton RL; Strongosky AJ; Uitti RJ; McCarthy A; Lynch T; Siuda J; Opala G; Rudzinska M; Krygowska-Wajs A; Barcikowska M; Czyzewski K; Puschmann A; Nishioka K; Funayama M; Hattori N; Parisi JE; Petersen RC; Graff-Radford NR; Boeve BF; Springer W; Wszolek ZK; Dickson DW; Ross OA
    Neurology; 2015 Dec; 85(23):2016-25. PubMed ID: 26561290
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Variations in the APP gene promoter region and risk of Alzheimer disease.
    Guyant-Maréchal L; Rovelet-Lecrux A; Goumidi L; Cousin E; Hannequin D; Raux G; Penet C; Ricard S; Macé S; Amouyel P; Deleuze JF; Frebourg T; Brice A; Lambert JC; Campion D
    Neurology; 2007 Feb; 68(9):684-7. PubMed ID: 17325276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Age-dependent association of KIBRA genetic variation and Alzheimer's disease risk.
    Rodríguez-Rodríguez E; Infante J; Llorca J; Mateo I; Sánchez-Quintana C; García-Gorostiaga I; Sánchez-Juan P; Berciano J; Combarros O
    Neurobiol Aging; 2009 Feb; 30(2):322-4. PubMed ID: 17707552
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cholesteryl Ester Transfer Protein (CETP) genotype and cognitive function in persons aged 35 years or older.
    Izaks GJ; van der Knaap AM; Gansevoort RT; Navis G; Slaets JP; Dullaart RP
    Neurobiol Aging; 2012 Aug; 33(8):1851.e7-16. PubMed ID: 22464147
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction.
    Elmas E; Bugert P; Popp T; Lang S; Weiss C; Behnes M; Borggrefe M; Kälsch T
    J Cardiovasc Electrophysiol; 2010 Nov; 21(11):1260-5. PubMed ID: 20586826
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.
    Guella I; Soldà G; Cilia R; Pezzoli G; Asselta R; Duga S; Goldwurm S
    Mov Disord; 2012 May; 27(6):800-1. PubMed ID: 22278960
    [No Abstract]   [Full Text] [Related]  

  • 19. Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
    Belzil VV; André-Guimont C; Atallah MR; Daoud H; Dupré N; Bouchard JP; Camu W; Dion PA; Rouleau GA
    Neurobiol Aging; 2012 Aug; 33(8):1845.e7-9. PubMed ID: 22361451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.