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 *

177 related articles for article (PubMed ID: 33810837)

  • 1. New advances in Amyotrophic Lateral Sclerosis genetics: Towards gene therapy opportunities for familial and young cases.
    Amador MD; Muratet F; Teyssou E; Boillée S; Millecamps S
    Rev Neurol (Paris); 2021 May; 177(5):524-535. PubMed ID: 33810837
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
    J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication.
    Libonati L; Cambieri C; Colavito D; Moret F; D'Andrea E; Del Giudice E; Leon A; Inghilleri M; Ceccanti M
    J Neurol; 2024 Apr; 271(4):1921-1936. PubMed ID: 38112783
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic variability in sporadic amyotrophic lateral sclerosis.
    Van Daele SH; Moisse M; van Vugt JJFA; Zwamborn RAJ; van der Spek R; van Rheenen W; Van Eijk K; Kenna K; Corcia P; Vourc'h P; Couratier P; Hardiman O; McLaughin R; Gotkine M; Drory V; Ticozzi N; Silani V; Ratti A; de Carvalho M; Mora Pardina JS; Povedano M; Andersen PM; Weber M; Başak NA; Shaw C; Shaw PJ; Morrison KE; Landers JE; Glass JD; van Es MA; van den Berg LH; Al-Chalabi A; Veldink J; Van Damme P
    Brain; 2023 Sep; 146(9):3760-3769. PubMed ID: 37043475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
    Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
    Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
    van Blitterswijk M; van Es MA; Hennekam EA; Dooijes D; van Rheenen W; Medic J; Bourque PR; Schelhaas HJ; van der Kooi AJ; de Visser M; de Bakker PI; Veldink JH; van den Berg LH
    Hum Mol Genet; 2012 Sep; 21(17):3776-84. PubMed ID: 22645277
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
    Bertolin C; D'Ascenzo C; Querin G; Gaiani A; Boaretto F; Salvoro C; Vazza G; Angelini C; Cagnin A; Pegoraro E; Sorarù G; Mostacciuolo ML
    Neurobiol Aging; 2014 May; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pre-symptomatic diagnosis in ALS.
    Corcia P; Lumbroso S; Cazeneuve C; Mouzat K; Camu W; Vourc'h P;
    Rev Neurol (Paris); 2020 Mar; 176(3):166-169. PubMed ID: 31932031
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Targeted next-generation sequencing study in familial ALS-FTD Portuguese patients negative for C9orf72 HRE.
    Gromicho M; Coutinho AM; Pronto-Laborinho AC; Raposeiro R; Tavares J; Antunes D; de Carvalho M
    J Neurol; 2020 Dec; 267(12):3578-3592. PubMed ID: 32638105
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients.
    Ivantsik O; John A; Kydonopoulou K; Mitropoulos K; Gerou S; Ali BR; Patrinos GP
    Genes (Basel); 2024 Feb; 15(3):. PubMed ID: 38540370
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
    Giannoccaro MP; Bartoletti-Stella A; Piras S; Pession A; De Massis P; Oppi F; Stanzani-Maserati M; Pasini E; Baiardi S; Avoni P; Parchi P; Liguori R; Capellari S
    J Neurol; 2017 Jul; 264(7):1426-1433. PubMed ID: 28620717
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of ALS and FTD: implications for translational studies.
    Liščić RM
    Arh Hig Rada Toksikol; 2015 Dec; 66(4):285-90. PubMed ID: 26751860
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetics insight into the amyotrophic lateral sclerosis/frontotemporal dementia spectrum.
    Ji AL; Zhang X; Chen WW; Huang WJ
    J Med Genet; 2017 Mar; 54(3):145-154. PubMed ID: 28087719
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease.
    Lattante S; Conte A; Zollino M; Luigetti M; Del Grande A; Marangi G; Romano A; Marcaccio A; Meleo E; Bisogni G; Rossini PM; Sabatelli M
    Neurology; 2012 Jul; 79(1):66-72. PubMed ID: 22722621
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center.
    Chadi G; Maximino JR; Jorge FMH; Borba FC; Gilio JM; Callegaro D; Lopes CG; Santos SND; Rebelo GNS
    Amyotroph Lateral Scler Frontotemporal Degener; 2017 May; 18(3-4):249-255. PubMed ID: 27978769
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China.
    Wei Q; Chen X; Chen Y; Ou R; Cao B; Hou Y; Zhang L; Shang HF
    Sci China Life Sci; 2019 Apr; 62(4):517-525. PubMed ID: 30863961
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.
    Fifita JA; Zhang KY; Galper J; Williams KL; McCann EP; Hogan AL; Saunders N; Bauer D; Tarr IS; Pamphlett R; Nicholson GA; Rowe D; Yang S; Blair IP
    Neurodegener Dis; 2017; 17(6):304-312. PubMed ID: 29131108
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance.
    Giannoccaro MP; Bartoletti-Stella A; Piras S; Casalena A; Oppi F; Ambrosetto G; Montagna P; Liguori R; Parchi P; Capellari S
    J Alzheimers Dis; 2018; 62(2):687-697. PubMed ID: 29480190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.