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 *

252 related articles for article (PubMed ID: 32897108)

  • 41. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts.
    Ingre C; Landers JE; Rizik N; Volk AE; Akimoto C; Birve A; Hübers A; Keagle PJ; Piotrowska K; Press R; Andersen PM; Ludolph AC; Weishaupt JH
    Neurobiol Aging; 2013 Jun; 34(6):1708.e1-6. PubMed ID: 23141414
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review.
    Wei Q; Zhou Q; Chen Y; Ou R; Cao B; Xu Y; Yang J; Shang HF
    Sci Rep; 2017 Mar; 7():44606. PubMed ID: 28291249
    [TBL] [Abstract][Full Text] [Related]  

  • 43. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.
    Baradaran-Heravi Y; Dillen L; Nguyen HP; Van Mossevelde S; Baets J; De Jonghe P; Engelborghs S; De Deyn PP; Vandenbulcke M; Vandenberghe R; Van Damme P; Cras P; Salmon E; Synofzik M; Heutink P; Wilke C; Simon-Sanchez J; Rojas-Garcia R; Turon-Sans J; Lleó A; Illán-Gala I; Clarimón J; Borroni B; Padovani A; Pastor P; Diez-Fairen M; Aguilar M; Gelpi E; Sanchez-Valle R; Borrego-Ecija S; Matej R; Parobkova E; Nacmias B; Sorbi S; Bagnoli S; de Mendonça A; Ferreira C; Fraidakis MJ; Diehl-Schmid J; Alexopoulos P; Almeida MR; Santana I; Van Broeckhoven C; van der Zee J; ;
    Neurobiol Aging; 2018 Sep; 69():293.e9-293.e11. PubMed ID: 29886022
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Genetic coherence between hereditary amyotrophic lateral sclerosis and frontotemporal dementia].
    Gjerde KV; Tysnes OB
    Tidsskr Nor Laegeforen; 2014 Feb; 134(3):302-6. PubMed ID: 24518478
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.
    Kim HJ; Kwon MJ; Choi WJ; Oh KW; Oh SI; Ki CS; Kim SH
    Neurobiol Aging; 2014 Aug; 35(8):1957.e7-8. PubMed ID: 24684794
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Delineating the relationship between amyotrophic lateral sclerosis and frontotemporal dementia: Sequence and structure-based predictions.
    Kumar V; Islam A; Hassan MI; Ahmad F
    Biochim Biophys Acta; 2016 Sep; 1862(9):1742-54. PubMed ID: 27318084
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genetic and Phenotypic Spectrum of Amyotrophic Lateral Sclerosis Patients with CCNF Variants from a Large Chinese Cohort.
    Zhao B; Jiang Q; Lin J; Wei Q; Li C; Hou Y; Cao B; Zhang L; Ou R; Liu K; Yang T; Xiao Y; Huang R; Shang H
    Mol Neurobiol; 2023 Jul; 60(7):4150-4160. PubMed ID: 37171577
    [TBL] [Abstract][Full Text] [Related]  

  • 48. PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.
    Chen Y; Zheng ZZ; Huang R; Chen K; Song W; Zhao B; Chen X; Yang Y; Yuan L; Shang HF
    Neurobiol Aging; 2013 Jul; 34(7):1922.e1-5. PubMed ID: 23428184
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical and neuropathological features of ALS/FTD with TIA1 mutations.
    Hirsch-Reinshagen V; Pottier C; Nicholson AM; Baker M; Hsiung GR; Krieger C; Sengdy P; Boylan KB; Dickson DW; Mesulam M; Weintraub S; Bigio E; Zinman L; Keith J; Rogaeva E; Zivkovic SA; Lacomis D; Taylor JP; Rademakers R; Mackenzie IRA
    Acta Neuropathol Commun; 2017 Dec; 5(1):96. PubMed ID: 29216908
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes.
    Schymick JC; Yang Y; Andersen PM; Vonsattel JP; Greenway M; Momeni P; Elder J; Chiò A; Restagno G; Robberecht W; Dahlberg C; Mukherjee O; Goate A; Graff-Radford N; Caselli RJ; Hutton M; Gass J; Cannon A; Rademakers R; Singleton AB; Hardiman O; Rothstein J; Hardy J; Traynor BJ
    J Neurol Neurosurg Psychiatry; 2007 Jul; 78(7):754-6. PubMed ID: 17371905
    [TBL] [Abstract][Full Text] [Related]  

  • 51. SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis.
    Wicks P; Abrahams S; Papps B; Al-Chalabi A; Shaw CE; Leigh PN; Goldstein LH
    J Neurol; 2009 Feb; 256(2):234-41. PubMed ID: 19252762
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The role of heat shock proteins in Amyotrophic Lateral Sclerosis: The therapeutic potential of Arimoclomol.
    Kalmar B; Lu CH; Greensmith L
    Pharmacol Ther; 2014 Jan; 141(1):40-54. PubMed ID: 23978556
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mutation Screening of the
    Li Y; Sun B; Wang Z; He Z; Yang F; Wang H; Cui F; Chen Z; Ling L; Wang C; Huang X
    Front Neurosci; 2021; 15():595775. PubMed ID: 34025336
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.
    Liu ZJ; Lin HX; Wei Q; Zhang QJ; Chen CX; Tao QQ; Liu GL; Ni W; Gitler AD; Li HF; Wu ZY
    Aging Dis; 2019 Dec; 10(6):1199-1206. PubMed ID: 31788332
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation screening and burden analysis of GLT8D1 in Chinese patients with amyotrophic lateral sclerosis.
    Cao B; Gu X; Wei Q; Li C; Chen Y; Ou R; Hou Y; Zhang L; Li T; Song W; Zhao B; Wu Y; Chen X; Shang H
    Neurobiol Aging; 2021 May; 101():298.e17-298.e21. PubMed ID: 33581933
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Novel mutation in optineurin causing aggressive ALS+/-frontotemporal dementia.
    Feng SM; Che CH; Feng SY; Liu CY; Li LY; Li YX; Huang HP; Zou ZY
    Ann Clin Transl Neurol; 2019 Dec; 6(12):2377-2383. PubMed ID: 31838784
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis.
    Del Bo R; Tiloca C; Pensato V; Corrado L; Ratti A; Ticozzi N; Corti S; Castellotti B; Mazzini L; Sorarù G; Cereda C; D'Alfonso S; Gellera C; Comi GP; Silani V;
    J Neurol Neurosurg Psychiatry; 2011 Nov; 82(11):1239-43. PubMed ID: 21613650
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A patient carrying a heterozygous p.Asn267Ser TARDBP missense mutation diagnosed as ALS and only involving lower motor neurons.
    Jin S; Sun Z; Fang X; Chen H; Yang W
    Neurol Sci; 2023 Feb; 44(2):777-782. PubMed ID: 36527522
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Rare
    Gu X; Chen Y; Wei Q; Hou Y; Cao B; Zhang L; Ou R; Lin J; Liu K; Zhao B; Shang H
    Front Genet; 2021; 12():740052. PubMed ID: 34868212
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.