163 related articles for article (PubMed ID: 37904013)
1. Hyperhidrosis as the initial symptom in FUS mutation-associated amyotrophic lateral sclerosis: a case report and comprehensive literature review.
Chen X; Luo J; Zheng W; Huang Q; Du C; Yuan H; Xiao F
Neurol Sci; 2024 Apr; 45(4):1523-1527. PubMed ID: 37904013
[TBL] [Abstract][Full Text] [Related]
2. 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]
3.
Lu T; Yang J; Luo L; Wei D
Amyotroph Lateral Scler Frontotemporal Degener; 2022 Nov; 23(7-8):580-584. PubMed ID: 35232295
[TBL] [Abstract][Full Text] [Related]
4.
Bazán-Rodríguez L; Ruíz-Avalos JA; Bernal-López O; Benitez-Alonso EO; Villaseñor-Sánchez J; Fernandez-Valverde F; Vargas-Cañas S
Neurocase; 2022 Jun; 28(3):323-330. PubMed ID: 35833217
[TBL] [Abstract][Full Text] [Related]
5. Sporadic Amyotrophic Lateral Sclerosis Due to a FUS P525L Mutation with Asymmetric Muscle Weakness and Anti-ganglioside Antibodies.
Tanemoto M; Hisahara S; Ikeda K; Yokokawa K; Manabe T; Tsuda R; Yamamoto D; Matsushita T; Matsumura A; Suzuki S; Shimohama S
Intern Med; 2021 Jun; 60(12):1949-1953. PubMed ID: 33518565
[TBL] [Abstract][Full Text] [Related]
6.
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]
7. 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]
8. 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]
9. Deficient RNA-editing enzyme ADAR2 in an amyotrophic lateral sclerosis patient with a FUS(P525L) mutation.
Aizawa H; Hideyama T; Yamashita T; Kimura T; Suzuki N; Aoki M; Kwak S
J Clin Neurosci; 2016 Oct; 32():128-9. PubMed ID: 27343041
[TBL] [Abstract][Full Text] [Related]
10. Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis.
Zou ZY; Che CH; Feng SY; Fang XY; Huang HP; Liu CY
Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):73-79. PubMed ID: 32720527
[TBL] [Abstract][Full Text] [Related]
11. Young-onset rapidly progressive ALS associated with heterozygous FUS mutation.
Gromicho M; Oliveira Santos M; Pinto A; Pronto-Laborinho A; De Carvalho M
Amyotroph Lateral Scler Frontotemporal Degener; 2017 Aug; 18(5-6):451-453. PubMed ID: 28288521
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation P525L (c.1574C > T) in FUS gene.
Akter M; Cui H; Abir Hosain M; Ding B
Stem Cell Res; 2023 Jun; 69():103103. PubMed ID: 37116345
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation.
Liu X; Chen J; Liu W; Li X; Chen Q; Liu T; Gao S; Deng M
Neurogenetics; 2015 Jul; 16(3):223-31. PubMed ID: 25912081
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature.
Picher-Martel V; Brunet F; Dupré N; Chrestian N
J Child Neurol; 2020 Jul; 35(8):556-562. PubMed ID: 32281455
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
