BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 33274538)

  • 21. Identification of PSEN1 and APP gene mutations in Korean patients with early-onset Alzheimer's disease.
    Park HK; Na DL; Lee JH; Kim JW; Ki CS
    J Korean Med Sci; 2008 Apr; 23(2):213-7. PubMed ID: 18437002
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Screening for Genetic Mutations Associated with Early-Onset Alzheimer's Disease in Han Chinese.
    Liu C; Cong L; Zhu M; Wang Y; Tang S; Han X; Zhang Q; Tian N; Liu K; Liang X; Fa W; Wang N; Hou T; Du Y
    Curr Alzheimer Res; 2022; 19(10):724-733. PubMed ID: 36306459
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Presenilin-1 (PSEN1) Mutations: Clinical Phenotypes beyond Alzheimer's Disease.
    Yang Y; Bagyinszky E; An SSA
    Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37176125
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.
    Roeber S; Müller-Sarnowski F; Kress J; Edbauer D; Kuhlmann T; Tüttelmann F; Schindler C; Winter P; Arzberger T; Müller U; Danek A; Kretzschmar HA
    J Neural Transm (Vienna); 2015 Dec; 122(12):1715-9. PubMed ID: 26350633
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and genetic characteristics in a central-southern Chinese cohort of early-onset Alzheimer's disease.
    Liang Z; Wu Y; Li C; Liu Z
    Front Neurol; 2023; 14():1119326. PubMed ID: 37051054
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years.
    Lacour M; Quenez O; Rovelet-Lecrux A; Salomon B; Rousseau S; Richard AC; Quillard-Muraine M; Pasquier F; Rollin-Sillaire A; Martinaud O; Zarea A; de la Sayette V; Boutoleau-Bretonniere C; Etcharry-Bouyx F; Chauviré V; Sarazin M; le Ber I; Epelbaum S; Jonveaux T; Rouaud O; Ceccaldi M; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Magnin E; Sauvée M; Marelli C; Gabelle A; Pariente J; Paquet C; Boland A; Deleuze JF; Campion D; Hannequin D; Nicolas G; Wallon D;
    J Alzheimers Dis; 2019; 71(1):227-243. PubMed ID: 31381512
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Two Novel Mutations and a
    Li YS; Yang ZH; Zhang Y; Yang J; Shang DD; Zhang SY; Wu J; Ji Y; Zhao L; Shi CH; Xu YM
    Aging Dis; 2019 Aug; 10(4):908-914. PubMed ID: 31440394
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular genetics of early-onset Alzheimer's disease revisited.
    Cacace R; Sleegers K; Van Broeckhoven C
    Alzheimers Dement; 2016 Jun; 12(6):733-48. PubMed ID: 27016693
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pathogenic variants in the Longitudinal Early-onset Alzheimer's Disease Study cohort.
    Nudelman KNH; Jackson T; Rumbaugh M; Eloyan A; Abreu M; Dage JL; Snoddy C; Faber KM; Foroud T; Hammers DB; ; Taurone A; Thangarajah M; Aisen P; Beckett L; Kramer J; Koeppe R; Kukull WA; Murray ME; Toga AW; Vemuri P; Atri A; Day GS; Duara R; Graff-Radford NR; Honig LS; Jones DT; Masdeu JC; Mendez M; Musiek E; Onyike CU; Riddle M; Rogalski E; Salloway S; Sha SJ; Turner RS; Wingo TS; Wolk DA; Carrillo MC; Dickerson BC; Rabinovici GD; Apostolova LG;
    Alzheimers Dement; 2023 Nov; 19 Suppl 9(Suppl 9):S64-S73. PubMed ID: 37801072
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The
    Almkvist O; Graff C
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946903
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
    Zekanowski C; Styczyńska M; Pepłońska B; Gabryelewicz T; Religa D; Ilkowski J; Kijanowska-Haładyna B; Kotapka-Minc S; Mikkelsen S; Pfeffer A; Barczak A; Łuczywek E; Wasiak B; Chodakowska-Zebrowska M; Gustaw K; Łaczkowski J; Sobów T; Kuźnicki J; Barcikowska M
    Exp Neurol; 2003 Dec; 184(2):991-6. PubMed ID: 14769392
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.
    Jiao B; Tang B; Liu X; Xu J; Wang Y; Zhou L; Zhang F; Yan X; Zhou Y; Shen L
    Neurobiol Aging; 2014 Aug; 35(8):1957.e1-6. PubMed ID: 24650794
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Amyloid-β
    Perrone F; Bjerke M; Hens E; Sieben A; Timmers M; De Roeck A; Vandenberghe R; Sleegers K; Martin JJ; De Deyn PP; Engelborghs S; van der Zee J; Van Broeckhoven C; Cacace R;
    Alzheimers Res Ther; 2020 Sep; 12(1):108. PubMed ID: 32917274
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Longitudinal cognitive decline in autosomal-dominant Alzheimer's disease varies with mutations in APP and PSEN1 genes.
    Almkvist O; Rodriguez-Vieitez E; Thordardottir S; Nordberg A; Viitanen M; Lannfelt L; Graff C
    Neurobiol Aging; 2019 Oct; 82():40-47. PubMed ID: 31386938
    [TBL] [Abstract][Full Text] [Related]  

  • 35.
    Youn YC; Jang JW; Han SH; Kim H; Seok JW; Byun JS; Park KY; An SSA; Chun IK; Kim S
    Clin Interv Aging; 2017; 12():1041-1048. PubMed ID: 28721032
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Early-Onset Alzheimer's Disease: What Is Missing in Research?
    Ayodele T; Rogaeva E; Kurup JT; Beecham G; Reitz C
    Curr Neurol Neurosci Rep; 2021 Jan; 21(2):4. PubMed ID: 33464407
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
    Raux G; Guyant-Maréchal L; Martin C; Bou J; Penet C; Brice A; Hannequin D; Frebourg T; Campion D
    J Med Genet; 2005 Oct; 42(10):793-5. PubMed ID: 16033913
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Genetic counseling and testing for families with Alzheimer's disease].
    Kowalska A
    Neurol Neurochir Pol; 2004; 38(6):495-501. PubMed ID: 15654674
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.
    Nicolas G; Wallon D; Charbonnier C; Quenez O; Rousseau S; Richard AC; Rovelet-Lecrux A; Coutant S; Le Guennec K; Bacq D; Garnier JG; Olaso R; Boland A; Meyer V; Deleuze JF; Munter HM; Bourque G; Auld D; Montpetit A; Lathrop M; Guyant-Maréchal L; Martinaud O; Pariente J; Rollin-Sillaire A; Pasquier F; Le Ber I; Sarazin M; Croisile B; Boutoleau-Bretonnière C; Thomas-Antérion C; Paquet C; Sauvée M; Moreaud O; Gabelle A; Sellal F; Ceccaldi M; Chamard L; Blanc F; Frebourg T; Campion D; Hannequin D
    Eur J Hum Genet; 2016 May; 24(5):710-6. PubMed ID: 26242991
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.
    Krüger J; Moilanen V; Majamaa K; Remes AM
    Alzheimer Dis Assoc Disord; 2012; 26(3):272-6. PubMed ID: 21959359
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.