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.
42. The repeat length of Tang L; Chen L; Liu X; He J; Ma Y; Zhang N; Fan D Front Neurol; 2022; 13():939775. PubMed ID: 35989899 [TBL] [Abstract][Full Text] [Related]
43. The genetics of motor neuron diseases. Figlewicz DA; Orrell RW Amyotroph Lateral Scler Other Motor Neuron Disord; 2003 Dec; 4(4):225-31. PubMed ID: 14753656 [TBL] [Abstract][Full Text] [Related]
44. Clinical profile of motor neuron disease patients with lower urinary tract symptoms and neurogenic bladder. Vázquez-Costa JF; Arlandis S; Hervas D; Martínez-Cuenca E; Cardona F; Pérez-Tur J; Broseta E; Sevilla T J Neurol Sci; 2017 Jul; 378():130-136. PubMed ID: 28566149 [TBL] [Abstract][Full Text] [Related]
45. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. Nishimura AL; Mitne-Neto M; Silva HC; Richieri-Costa A; Middleton S; Cascio D; Kok F; Oliveira JR; Gillingwater T; Webb J; Skehel P; Zatz M Am J Hum Genet; 2004 Nov; 75(5):822-31. PubMed ID: 15372378 [TBL] [Abstract][Full Text] [Related]
46. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Nuytemans K; Bademci G; Kohli MM; Beecham GW; Wang L; Young JI; Nahab F; Martin ER; Gilbert JR; Benatar M; Haines JL; Scott WK; Züchner S; Pericak-Vance MA; Vance JM Ann Hum Genet; 2013 Sep; 77(5):351-63. PubMed ID: 23845100 [TBL] [Abstract][Full Text] [Related]
47. Linking amyotrophic lateral sclerosis and spinal muscular atrophy through RNA-transcriptome homeostasis: a genomics perspective. Gama-Carvalho M; L Garcia-Vaquero M; R Pinto F; Besse F; Weis J; Voigt A; Schulz JB; De Las Rivas J J Neurochem; 2017 Apr; 141(1):12-30. PubMed ID: 28054357 [TBL] [Abstract][Full Text] [Related]
48. Genetic determination of motor neuron disease and neuropathy. Vrebalov Cindro P; Vrebalov Cindro V Coll Antropol; 2015 Mar; 39(1):261-5. PubMed ID: 26040103 [TBL] [Abstract][Full Text] [Related]
49. The history behind ALS type 8: from the first phenotype description to the discovery of VAPB mutation. Novis LE; Spitz M; Teive HAG Arq Neuropsiquiatr; 2021 Aug; 79(8):743-747. PubMed ID: 34133501 [TBL] [Abstract][Full Text] [Related]
50. [Gene Therapies in Motor Neuron Diseases ALS and SMA]. Günther R Fortschr Neurol Psychiatr; 2023 Apr; 91(4):153-163. PubMed ID: 36822211 [TBL] [Abstract][Full Text] [Related]
51. A polymorphism in the poliovirus receptor gene differs in motor neuron disease. Saunderson R; Yu B; Trent RJ; Pamphlett R Neuroreport; 2004 Feb; 15(2):383-6. PubMed ID: 15076773 [TBL] [Abstract][Full Text] [Related]
52. Atypical motor neuron disease with bent spine clinical onset and long survival carrying C9orf72 expansion. Santarelli M; De Giglio L; Altavista MC; Chiò A; Pennisi EM Neurol Sci; 2021 Jan; 42(1):353-355. PubMed ID: 32683569 [No Abstract] [Full Text] [Related]
53. Emerging antisense oligonucleotide and viral therapies for amyotrophic lateral sclerosis. Ly CV; Miller TM Curr Opin Neurol; 2018 Oct; 31(5):648-654. PubMed ID: 30028737 [TBL] [Abstract][Full Text] [Related]
54. Functional Roles of Long Non-coding RNAs in Motor Neuron Development and Disease. Chen KW; Chen JA J Biomed Sci; 2020 Feb; 27(1):38. PubMed ID: 32093746 [TBL] [Abstract][Full Text] [Related]
55. Parkinson's disease, amyotrophic lateral sclerosis and spinal muscular atrophy are caused by an unstable (CAG)n trinucleotide repeat microsatellite. Fischer KM Med Hypotheses; 1997 Oct; 49(4):337-45. PubMed ID: 9352504 [No Abstract] [Full Text] [Related]
56. Differential diagnosis between amyotrophic lateral sclerosis and spinal muscular atrophy by skin involvement. Ono S; Mannen T; Toyokura Y J Neurol Sci; 1989 Jul; 91(3):301-10. PubMed ID: 2769298 [TBL] [Abstract][Full Text] [Related]
57. More than one locus for familial amyotrophic lateral sclerosis: absence of linkage to the SMA locus. King AW; Orrell RW; Lane R; de Belleroche JS Biochem Soc Trans; 1994 May; 22(2):149S. PubMed ID: 7958219 [No Abstract] [Full Text] [Related]
59. Noncoding repeat expansions for ALS in Japan are associated with the Hirano M; Samukawa M; Isono C; Saigoh K; Nakamura Y; Kusunoki S Neurol Genet; 2018 Aug; 4(4):e252. PubMed ID: 30109267 [TBL] [Abstract][Full Text] [Related]
60. Modern approaches in gene therapy of motor neuron diseases. Zakharova M Med Res Rev; 2021 Sep; 41(5):2634-2655. PubMed ID: 32638429 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]