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Journal Abstract Search

521 related items for PubMed ID: 30870681

  • 1. Genetics of amyotrophic lateral sclerosis: A review.
    Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL.
    J Neurol Sci; 2019 Apr 15; 399():217-226. PubMed ID: 30870681
    [Abstract] [Full Text] [Related]

  • 2. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
    Edgar S, Ellis M, Abdul-Aziz NA, Goh KJ, Shahrizaila N, Kennerson ML, Ahmad-Annuar A.
    Neurobiol Aging; 2021 Dec 15; 108():200-206. PubMed ID: 34404558
    [Abstract] [Full Text] [Related]

  • 3. [Genetic counselling is relevant in familial as well as sporadic cases of amyotrophic lateral sclerosis].
    Lindquist SG, Dunø M, Svenstrup K, Nielsen JE.
    Ugeskr Laeger; 2014 Oct 20; 176(43):. PubMed ID: 25353674
    [Abstract] [Full Text] [Related]

  • 4. Genetics of amyotrophic lateral sclerosis.
    Corcia P, Couratier P, Blasco H, Andres CR, Beltran S, Meininger V, Vourc'h P.
    Rev Neurol (Paris); 2017 May 20; 173(5):254-262. PubMed ID: 28449881
    [Abstract] [Full Text] [Related]

  • 5. Genetics of familial Amyotrophic lateral sclerosis.
    Ticozzi N, Tiloca C, Morelli C, Colombrita C, Poletti B, Doretti A, Maderna L, Messina S, Ratti A, Silani V.
    Arch Ital Biol; 2011 Mar 20; 149(1):65-82. PubMed ID: 21412717
    [Abstract] [Full Text] [Related]

  • 6. Connecting RNA-Modifying Similarities of TDP-43, FUS, and SOD1 with MicroRNA Dysregulation Amidst A Renewed Network Perspective of Amyotrophic Lateral Sclerosis Proteinopathy.
    Pham J, Keon M, Brennan S, Saksena N.
    Int J Mol Sci; 2020 May 14; 21(10):. PubMed ID: 32422969
    [Abstract] [Full Text] [Related]

  • 7. Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia.
    Marjanović IV, Selak-Djokić B, Perić S, Janković M, Arsenijević V, Basta I, Lavrnić D, Stefanova E, Stević Z.
    J Neurol; 2017 Jun 14; 264(6):1091-1098. PubMed ID: 28444446
    [Abstract] [Full Text] [Related]

  • 8. Motoneuron Disease: Basic Science.
    Ilieva H, Maragakis NJ.
    Adv Neurobiol; 2017 Jun 14; 15():163-190. PubMed ID: 28674981
    [Abstract] [Full Text] [Related]

  • 9. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
    Müller K, Brenner D, Weydt P, Meyer T, Grehl T, Petri S, Grosskreutz J, Schuster J, Volk AE, Borck G, Kubisch C, Klopstock T, Zeller D, Jablonka S, Sendtner M, Klebe S, Knehr A, Günther K, Weis J, Claeys KG, Schrank B, Sperfeld AD, Hübers A, Otto M, Dorst J, Meitinger T, Strom TM, Andersen PM, Ludolph AC, Weishaupt JH, German ALS network MND-NET.
    J Neurol Neurosurg Psychiatry; 2018 Aug 14; 89(8):817-827. PubMed ID: 29650794
    [Abstract] [Full Text] [Related]

  • 10. 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 14; 49(4):258-63. PubMed ID: 22499346
    [Abstract] [Full Text] [Related]

  • 11. CRISPR/Cas9-Mediated Gene Correction to Understand ALS.
    Yun Y, Ha Y.
    Int J Mol Sci; 2020 May 27; 21(11):. PubMed ID: 32471232
    [Abstract] [Full Text] [Related]

  • 12. From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis.
    Alrafiah AR.
    In Vivo; 2018 May 27; 32(5):983-998. PubMed ID: 30150420
    [Abstract] [Full Text] [Related]

  • 13. Protein folding alterations in amyotrophic lateral sclerosis.
    Parakh S, Atkin JD.
    Brain Res; 2016 Oct 01; 1648(Pt B):633-649. PubMed ID: 27064076
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
    [Abstract] [Full Text] [Related]

  • 15. 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 08; 6():32478. PubMed ID: 27604643
    [Abstract] [Full Text] [Related]

  • 16. The genetics of amyotrophic lateral sclerosis.
    Nijs M, Van Damme P.
    Curr Opin Neurol; 2024 Oct 01; 37(5):560-569. PubMed ID: 38967083
    [Abstract] [Full Text] [Related]

  • 17. Amyotrophic lateral sclerosis patients with various gene mutations show diverse motor phenotypes and survival in China.
    Jiang Q, Lin J, Wei Q, Yang T, Hou Y, Zhang L, Ou R, Xiao Y, Wang S, Zheng X, Li C, Shang H.
    J Med Genet; 2024 Aug 29; 61(9):839-846. PubMed ID: 38886047
    [Abstract] [Full Text] [Related]

  • 18. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan.
    Akiyama T, Warita H, Kato M, Nishiyama A, Izumi R, Ikeda C, Kamada M, Suzuki N, Aoki M.
    Muscle Nerve; 2016 Sep 29; 54(3):398-404. PubMed ID: 26823199
    [Abstract] [Full Text] [Related]

  • 19. Genetic epidemiology of familial ALS in Brazil.
    Nunes Gonçalves JP, Leoni TB, Martins MP, Peluzzo TM, Dourado MET, Saute JAM, Paranhos Miranda Covaleski AP, Bulle de Oliveira AS, Claudino R, Marques W, Nucci A, França MC.
    Neurobiol Aging; 2021 Jun 29; 102():227.e1-227.e4. PubMed ID: 33618928
    [Abstract] [Full Text] [Related]

  • 20. Estimated Prevalence and Incidence of Amyotrophic Lateral Sclerosis and SOD1 and C9orf72 Genetic Variants.
    Brown CA, Lally C, Kupelian V, Flanders WD.
    Neuroepidemiology; 2021 Jun 29; 55(5):342-353. PubMed ID: 34247168
    [Abstract] [Full Text] [Related]

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