123 related articles for article (PubMed ID: 35481267)
1. Analysis of
Wang F; Liu X; He J; Zhang N; Chen L; Tang L; Fan D
Front Neurol; 2022; 13():865264. PubMed ID: 35481267
[No Abstract] [Full Text] [Related]
2. Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.
Liu ZJ; Lin HX; Wei Q; Zhang QJ; Chen CX; Tao QQ; Liu GL; Ni W; Gitler AD; Li HF; Wu ZY
Aging Dis; 2019 Dec; 10(6):1199-1206. PubMed ID: 31788332
[TBL] [Abstract][Full Text] [Related]
3. Novel Variants in the
Liu CY; Lin JL; Feng SY; Che CH; Huang HP; Zou ZY
J Clin Neurol; 2022 Jan; 18(1):41-47. PubMed ID: 35021275
[TBL] [Abstract][Full Text] [Related]
4. Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients.
Narain P; Padhi AK; Dave U; Mishra D; Bhatia R; Vivekanandan P; Gomes J
Neurogenetics; 2019 Oct; 20(4):197-208. PubMed ID: 31432357
[TBL] [Abstract][Full Text] [Related]
5. Rare
Gu X; Chen Y; Wei Q; Hou Y; Cao B; Zhang L; Ou R; Lin J; Liu K; Zhao B; Shang H
Front Genet; 2021; 12():740052. PubMed ID: 34868212
[No Abstract] [Full Text] [Related]
6. Validation of the pathogenic role of rare DNAJC7 variants in Chinese patients with amyotrophic lateral sclerosis.
He J; Ma X; Yu W; Tang L; Fu J; Liu X; Ye S; Wan M; Fan D
Neurobiol Aging; 2021 Oct; 106():314.e1-314.e6. PubMed ID: 34233860
[TBL] [Abstract][Full Text] [Related]
7. Identification and characterization of novel ERBB4 variant associated with sporadic amyotrophic lateral sclerosis (ALS).
Kwon Y; Kang M; Jeon YM; Lee S; Lee HW; Park JS; Kim HJ
J Neurol Sci; 2024 Feb; 457():122885. PubMed ID: 38278691
[TBL] [Abstract][Full Text] [Related]
8. ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
Takahashi Y; Fukuda Y; Yoshimura J; Toyoda A; Kurppa K; Moritoyo H; Belzil VV; Dion PA; Higasa K; Doi K; Ishiura H; Mitsui J; Date H; Ahsan B; Matsukawa T; Ichikawa Y; Moritoyo T; Ikoma M; Hashimoto T; Kimura F; Murayama S; Onodera O; Nishizawa M; Yoshida M; Atsuta N; Sobue G; ; Fifita JA; Williams KL; Blair IP; Nicholson GA; Gonzalez-Perez P; Brown RH; Nomoto M; Elenius K; Rouleau GA; Fujiyama A; Morishita S; Goto J; Tsuji S
Am J Hum Genet; 2013 Nov; 93(5):900-5. PubMed ID: 24119685
[TBL] [Abstract][Full Text] [Related]
9. Presence of Rare Variants is Associated with Poorer Survival in Chinese Patients with Amyotrophic Lateral Sclerosis.
Dong S; Yin X; Wang K; Yang W; Li J; Wang Y; Zhou Y; Liu X; Wang J; Chen X
Phenomics; 2023 Apr; 3(2):167-181. PubMed ID: 37197644
[TBL] [Abstract][Full Text] [Related]
10. Mutation Screening of the
Li Y; Sun B; Wang Z; He Z; Yang F; Wang H; Cui F; Chen Z; Ling L; Wang C; Huang X
Front Neurosci; 2021; 15():595775. PubMed ID: 34025336
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review.
Wei Q; Zhou Q; Chen Y; Ou R; Cao B; Xu Y; Yang J; Shang HF
Sci Rep; 2017 Mar; 7():44606. PubMed ID: 28291249
[TBL] [Abstract][Full Text] [Related]
13. Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China.
Ni J; Liu Z; Li W; Yuan Y; Huang L; Hu Y; Liu P; Hou X; Jiao B; Li J; Shen L; Jiang H; Tang B; Wang J
Neurobiol Aging; 2021 Jan; 97():145.e17-145.e22. PubMed ID: 32690342
[TBL] [Abstract][Full Text] [Related]
14. Rare DNAJC7 Variants May Play a Minor Role in Chinese Patients with ALS.
Wang S; Zheng X; Wei Q; Lin J; Yang T; Xiao Y; Jiang Q; Li C; Shang H
Mol Neurobiol; 2024 Apr; 61(4):2265-2269. PubMed ID: 37870677
[TBL] [Abstract][Full Text] [Related]
15. Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan.
Tsai PC; Liao YC; Jih KY; Soong BW; Lin KP; Lee YC
Neurobiol Aging; 2018 Dec; 72():188.e1-188.e2. PubMed ID: 30054183
[TBL] [Abstract][Full Text] [Related]
16. Incidence of pathogenic, likely pathogenic, and uncertain ALS variants in a clinic cohort.
Roggenbuck J; Palettas M; Vicini L; Patel R; Quick A; Kolb SJ
Neurol Genet; 2020 Feb; 6(1):e390. PubMed ID: 32042918
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Screening for
Tian D; Li J; Tang L; Zhang N; Fan D
Front Aging Neurosci; 2018; 10():185. PubMed ID: 30008669
[TBL] [Abstract][Full Text] [Related]
19.
Zhang K; Liu Q; Liu K; Shen D; Tai H; Shu S; Ding Q; Fu H; Liu S; Wang Z; Li X; Liu M; Zhang X; Cui L
Neurol Genet; 2018 Jun; 4(3):e237. PubMed ID: 29845112
[TBL] [Abstract][Full Text] [Related]
20. Altered immunoreactivity of ErbB4, a causative gene product for ALS19, in the spinal cord of patients with sporadic ALS.
Takahashi Y; Uchino A; Shioya A; Sano T; Matsumoto C; Numata-Uematsu Y; Nagano S; Araki T; Murayama S; Saito Y
Neuropathology; 2019 Aug; 39(4):268-278. PubMed ID: 31124187
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
