PubMed for id: 867363

Year	Number of Results
1973	1
1975	1
1976	3
1977	1
1979	3
1980	3
1981	3
1982	4
1983	2
1984	4
1985	2
1986	6
1988	2
1989	7
1990	4
1991	9
1992	1
1993	4
1994	3
1995	3
1996	5
1997	3
1998	2
1999	3
2000	4
2001	8
2002	1
2003	4
2004	3
2005	3
2006	2
2007	4
2008	4
2009	2
2010	6
2011	5
2012	4
2013	6
2014	4
2015	6
2016	4
2017	5
2018	3
2019	8
2020	5
2021	10
2022	12
2023	5
2024	2

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. Chen X, et al. Neurol Sci. 2024 Apr;45(4):1523-1527. doi: 10.1007/s10072-023-07141-9. Epub 2023 Oct 31. Neurol Sci. 2024. PMID: 37904013 Review.

2

Multisystem pathology in McLeod syndrome.

Schon KR, O'Donovan DG, Briggs M, Rowe JB, Wijesekera L, Chinnery PF, van den Ameele J. Schon KR, et al. Neuropathology. 2024 Apr;44(2):109-114. doi: 10.1111/neup.12935. Epub 2023 Jul 12. Neuropathology. 2024. PMID: 37438874

3

Genotype and clinical phenotype analysis of a Family with Kennedy disease.

Cai BC, Zhong LF, Liu YH, Sui ZY, Yang Q, Zeng DT, Li X, Xu WD, Chen T. Cai BC, et al. Medicine (Baltimore). 2023 Apr 14;102(15):e33502. doi: 10.1097/MD.0000000000033502. Medicine (Baltimore). 2023. PMID: 37058074 Free PMC article.

4

Molecular Characterization of Non-Neurogenic and Neurogenic Lower Urinary Tract Dysfunction (LUTD) in SCI-Induced and Partial Bladder Outlet Obstruction Mouse Models.

von Siebenthal M, Akshay A, Besic M, Schneider MP, Hashemi Gheinani A, Burkhard FC, Monastyrskaya K. von Siebenthal M, et al. Int J Mol Sci. 2023 Jan 26;24(3):2451. doi: 10.3390/ijms24032451. Int J Mol Sci. 2023. PMID: 36768773 Free PMC article.

5

Expanding the spectrum of KIF5A mutations-case report of a large kindred with familial ALS and overlapping syndrome.

Dulski J, Strongosky AJ, Al-Shaikh RH, Wszolek ZK. Dulski J, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2023 May;24(3-4):347-350. doi: 10.1080/21678421.2022.2164204. Epub 2023 Jan 5. Amyotroph Lateral Scler Frontotemporal Degener. 2023. PMID: 36604770

6

Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series.

Shen X, Zhang J, Zhan F, Tian W, Jiang Q, Luan X, Zhang X, Cao L. Shen X, et al. Biomolecules. 2022 Sep 27;12(10):1382. doi: 10.3390/biom12101382. Biomolecules. 2022. PMID: 36291591 Free PMC article.

7

Optic neuritis in CD59 deficiency: an extremely rare presentation.

Günay Ç, Yardım E, Yaşar E, Hız-Kurul AS, Uzan GS, Öztürk T, Yaman A, Yiş U. Günay Ç, et al. Turk J Pediatr. 2022;64(4):787-794. doi: 10.24953/turkjped.2021.1405. Turk J Pediatr. 2022. PMID: 36082655 Free article.

8

Muscle and skin fibroblast TDP-43 expression, dynamic mutation analysis of NOTCH2NLC and C9orf72 in patients with FOSMN.

Liu Z, Guo X, Guo H, Luo J, Xiao F. Liu Z, et al. Neurol Sci. 2022 Nov;43(11):6505-6510. doi: 10.1007/s10072-022-06339-7. Epub 2022 Aug 16. Neurol Sci. 2022. PMID: 35974122

9

Clinical phenotype of familial amyotrophic lateral sclerosis with SOD1 gene mutation mimicking proximal myopathy: A case report and literature review.

Sun JM, Zhang CJ, Wang L, Bi HY. Sun JM, et al. Clin Neuropathol. 2022 Sep-Oct;41(5):219-225. doi: 10.5414/NP301459. Clin Neuropathol. 2022. PMID: 35652543 Review.

10

GGC repeat expansions in NOTCH2NLC causing a phenotype of lower motor neuron syndrome.

Zhang W, Ma J, Shi J, Huang S, Zhao R, Pang X, Wang J, Guo J, Chang X. Zhang W, et al. J Neurol. 2022 Aug;269(8):4469-4477. doi: 10.1007/s00415-022-11092-0. Epub 2022 Apr 2. J Neurol. 2022. PMID: 35366689

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

184 results

Results by year