184 related articles for article (PubMed ID: 34074186)
1. A case of juvenile-onset amyotrophic lateral sclerosis with a
Wu Y; Li C; Yang T; Lin J; Shang H
Amyotroph Lateral Scler Frontotemporal Degener; 2022 May; 23(3-4):313-314. PubMed ID: 34074186
[TBL] [Abstract][Full Text] [Related]
2. A de novo c.1509dupA:p.R503fs mutation of
Chen L; Li J; Lu H; Liu Y
Amyotroph Lateral Scler Frontotemporal Degener; 2020 Nov; 21(7-8):635-637. PubMed ID: 32501131
[TBL] [Abstract][Full Text] [Related]
3. The investigation of genetic and clinical features in Chinese patients with juvenile amyotrophic lateral sclerosis.
Liu ZJ; Lin HX; Liu GL; Tao QQ; Ni W; Xiao BG; Wu ZY
Clin Genet; 2017 Sep; 92(3):267-273. PubMed ID: 28429524
[TBL] [Abstract][Full Text] [Related]
4. Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations.
Wang P; Wei Q; Li H; Wu ZY
Chin Med J (Engl); 2023 Jan; 136(2):176-183. PubMed ID: 36801857
[TBL] [Abstract][Full Text] [Related]
5. FUS mutation is probably the most common pathogenic gene for JALS, especially sporadic JALS.
Chen L
Rev Neurol (Paris); 2021 Apr; 177(4):333-340. PubMed ID: 33036763
[TBL] [Abstract][Full Text] [Related]
6. A rare case of juvenile amyotrophic lateral sclerosis.
Bodur M; Toker RT; Başak AN; Okan MS
Turk J Pediatr; 2021; 63(3):495-499. PubMed ID: 34254495
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical and Genetic Features of Patients with Juvenile Amyotrophic Lateral Sclerosis with Fused in Sarcoma (FUS) Mutation.
Yu X; Zhao Z; Shen H; Bing Q; Li N; Hu J
Med Sci Monit; 2018 Dec; 24():8750-8757. PubMed ID: 30507891
[TBL] [Abstract][Full Text] [Related]
9. Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS/TLS: possible association of mental retardation with this mutation.
Yamashita S; Mori A; Sakaguchi H; Suga T; Ishihara D; Ueda A; Yamashita T; Maeda Y; Uchino M; Hirano T
J Neurol; 2012 Jun; 259(6):1039-44. PubMed ID: 22057404
[TBL] [Abstract][Full Text] [Related]
10. Juvenile-onset Sporadic Amyotrophic Lateral Sclerosis with a Frameshift FUS Gene Mutation Presenting Unique Neuroradiological Findings and Cognitive Impairment.
Hirayanagi K; Sato M; Furuta N; Makioka K; Ikeda Y
Intern Med; 2016; 55(6):689-93. PubMed ID: 26984092
[TBL] [Abstract][Full Text] [Related]
11. Amyotrophic Lateral Sclerosis after Receiving the Human Papilloma Virus Vaccine: A Case Report of a 15-year-old Girl.
Hikiami R; Yamakado H; Tatsumi S; Ayaki T; Hashi Y; Yamashita H; Sawamoto N; Tsuji T; Urushitani M; Takahashi R
Intern Med; 2018 Jul; 57(13):1917-1919. PubMed ID: 29434138
[TBL] [Abstract][Full Text] [Related]
12. P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.
Conte A; Lattante S; Zollino M; Marangi G; Luigetti M; Del Grande A; Servidei S; Trombetta F; Sabatelli M
Neuromuscul Disord; 2012 Jan; 22(1):73-5. PubMed ID: 21907581
[TBL] [Abstract][Full Text] [Related]
13. A juvenile sporadic amyotrophic lateral sclerosis case with P525L mutation in the FUS gene: A rare co-occurrence of autism spectrum disorder and tremor.
Eura N; Sugie K; Suzuki N; Kiriyama T; Izumi T; Shimakura N; Kato M; Aoki M
J Neurol Sci; 2019 Mar; 398():67-68. PubMed ID: 30684766
[No Abstract] [Full Text] [Related]
14. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
Hübers A; Just W; Rosenbohm A; Müller K; Marroquin N; Goebel I; Högel J; Thiele H; Altmüller J; Nürnberg P; Weishaupt JH; Kubisch C; Ludolph AC; Volk AE
Neurobiol Aging; 2015 Nov; 36(11):3117.e1-3117.e6. PubMed ID: 26362943
[TBL] [Abstract][Full Text] [Related]
15. Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.
Belzil VV; Langlais JS; Daoud H; Dion PA; Brais B; Rouleau GA
Arch Neurol; 2012 May; 69(5):653-6. PubMed ID: 22248478
[TBL] [Abstract][Full Text] [Related]
16. 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]
17.
Xiao X; Li M; Ye Z; He X; Wei J; Zha Y
Amyotroph Lateral Scler Frontotemporal Degener; 2024 Feb; 25(1-2):1-15. PubMed ID: 37926865
[TBL] [Abstract][Full Text] [Related]
18. Chorea is a pleiotropic clinical feature of mutated fused-in-sarcoma in amyotrophic lateral sclerosis.
Flies CM; Veldink JH
Amyotroph Lateral Scler Frontotemporal Degener; 2020 May; 21(3-4):309-311. PubMed ID: 32116048
[TBL] [Abstract][Full Text] [Related]
19. FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders.
Zhou B; Wang H; Cai Y; Wen H; Wang L; Zhu M; Chen Y; Yu Y; Lu X; Zhou M; Fang P; Li X; Hong D
Brain Behav; 2020 Jun; 10(6):e01625. PubMed ID: 32307925
[TBL] [Abstract][Full Text] [Related]
20. FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.
Neumann M; Bentmann E; Dormann D; Jawaid A; DeJesus-Hernandez M; Ansorge O; Roeber S; Kretzschmar HA; Munoz DG; Kusaka H; Yokota O; Ang LC; Bilbao J; Rademakers R; Haass C; Mackenzie IR
Brain; 2011 Sep; 134(Pt 9):2595-609. PubMed ID: 21856723
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
