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 *

171 related articles for article (PubMed ID: 36247987)

  • 21. Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.
    Borroni B; Bonvicini C; Alberici A; Buratti E; Agosti C; Archetti S; Papetti A; Stuani C; Di Luca M; Gennarelli M; Padovani A
    Hum Mutat; 2009 Nov; 30(11):E974-83. PubMed ID: 19655382
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.
    Vanden Broeck L; Kleinberger G; Chapuis J; Gistelinck M; Amouyel P; Van Broeckhoven C; Lambert JC; Callaerts P; Dermaut B
    Neurobiol Aging; 2015 Feb; 36(2):1121-9. PubMed ID: 25442115
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel S379A TARDBP mutation associated to late-onset sporadic ALS.
    Sprovieri T; Ungaro C; Perrone B; Naimo GD; Spataro R; Cavallaro S; La Bella V; Conforti FL
    Neurol Sci; 2019 Oct; 40(10):2111-2118. PubMed ID: 31165305
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
    Daoud H; Valdmanis PN; Kabashi E; Dion P; Dupré N; Camu W; Meininger V; Rouleau GA
    J Med Genet; 2009 Feb; 46(2):112-4. PubMed ID: 18931000
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic and clinical features of Chinese sporadic amyotrophic lateral sclerosis patients with TARDBP mutations.
    Feng F; Wang H; Liu J; Wang Z; Xu B; Zhao K; Tao X; He Z; Yang F; Huang X
    Brain Behav; 2021 Aug; 11(8):e2312. PubMed ID: 34333853
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosis.
    Solski JA; Yang S; Nicholson GA; Luquin N; Williams KL; Fernando R; Pamphlett R; Blair IP
    Amyotroph Lateral Scler; 2012 Sep; 13(5):465-70. PubMed ID: 22424122
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.
    Seltman RE; Matthews BR
    CNS Drugs; 2012 Oct; 26(10):841-70. PubMed ID: 22950490
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.
    Karch CM; Wen N; Fan CC; Yokoyama JS; Kouri N; Ross OA; Höglinger G; Müller U; Ferrari R; Hardy J; Schellenberg GD; Sleiman PM; Momeni P; Hess CP; Miller BL; Sharma M; Van Deerlin V; Smeland OB; Andreassen OA; Dale AM; Desikan RS;
    JAMA Neurol; 2018 Jul; 75(7):860-875. PubMed ID: 29630712
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.
    Kühnlein P; Sperfeld AD; Vanmassenhove B; Van Deerlin V; Lee VM; Trojanowski JQ; Kretzschmar HA; Ludolph AC; Neumann M
    Arch Neurol; 2008 Sep; 65(9):1185-9. PubMed ID: 18779421
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.
    Synofzik M; Born C; Rominger A; Lummel N; Schöls L; Biskup S; Schüle C; Grasshoff U; Klopstock T; Adamczyk C
    Neurobiol Aging; 2014 May; 35(5):1212.e1-5. PubMed ID: 24300238
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Enlarging clinical spectrum of FALS with TARDBP gene mutations: S393L variant in an Italian family showing phenotypic variability and relevance for genetic counselling.
    Origone P; Caponnetto C; Bandettini Di Poggio M; Ghiglione E; Bellone E; Ferrandes G; Mancardi GL; Mandich P
    Amyotroph Lateral Scler; 2010; 11(1-2):223-7. PubMed ID: 19714537
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Expanding the phenotype of
    Kacem I; Sghaier I; Ticozzi N; Mrabet S; Paverelli S; Nasri A; Ratti A; Ben Djebara M; Gargouri-Berrachid A; Silani V; Gouider R
    Amyotroph Lateral Scler Frontotemporal Degener; 2022 Nov; 23(7-8):623-626. PubMed ID: 35793404
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic architecture of ALS in Sardinia.
    Borghero G; Pugliatti M; Marrosu F; Marrosu MG; Murru MR; Floris G; Cannas A; Parish LD; Occhineri P; Cau TB; Loi D; Ticca A; Traccis S; Manera U; Canosa A; Moglia C; Calvo A; Barberis M; Brunetti M; Pliner HA; Renton AE; Nalls MA; Traynor BJ; Restagno G; Chiò A;
    Neurobiol Aging; 2014 Dec; 35(12):2882.e7-2882.e12. PubMed ID: 25123918
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
    Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family.
    Praline J; Vourc'h P; Guennoc AM; Veyrat-Durebex C; Corcia P
    Amyotroph Lateral Scler; 2012 Jan; 13(1):155-7. PubMed ID: 21830990
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.
    Rizzo G; Martinelli P; Manners D; Scaglione C; Tonon C; Cortelli P; Malucelli E; Capellari S; Testa C; Parchi P; Montagna P; Barbiroli B; Lodi R
    Brain; 2008 Oct; 131(Pt 10):2690-700. PubMed ID: 18819991
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Plasma Biomarkers Differentiate Parkinson's Disease From Atypical Parkinsonism Syndromes.
    Lin CH; Yang SY; Horng HE; Yang CC; Chieh JJ; Chen HH; Liu BH; Chiu MJ
    Front Aging Neurosci; 2018; 10():123. PubMed ID: 29755341
    [No Abstract]   [Full Text] [Related]  

  • 38. Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis.
    Kirby J; Goodall EF; Smith W; Highley JR; Masanzu R; Hartley JA; Hibberd R; Hollinger HC; Wharton SB; Morrison KE; Ince PG; McDermott CJ; Shaw PJ
    Neurogenetics; 2010 May; 11(2):217-25. PubMed ID: 19760257
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindred.
    Williams KL; Durnall JC; Thoeng AD; Warraich ST; Nicholson GA; Blair IP
    J Neurol Neurosurg Psychiatry; 2009 Nov; 80(11):1286-8. PubMed ID: 19864664
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
    Yan J; Deng HX; Siddique N; Fecto F; Chen W; Yang Y; Liu E; Donkervoort S; Zheng JG; Shi Y; Ahmeti KB; Brooks B; Engel WK; Siddique T
    Neurology; 2010 Aug; 75(9):807-14. PubMed ID: 20668259
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.