Similar articles for PMID: 37257665

Year	Number of Results
1996	1
1999	1
2000	2
2002	1
2003	1
2004	2
2005	2
2006	2
2009	1
2010	1
2011	8
2012	3
2013	4
2014	4
2015	12
2016	8
2017	8
2018	8
2019	10
2020	12
2021	11
2022	9
2023	3
2024	0

1

VRK1 variants at the cross road of Cajal body neuropathogenic mechanisms in distal neuropathies and motor neuron diseases.

Lazo PA, Morejón-García P. Lazo PA, et al. Neurobiol Dis. 2023 Jul;183:106172. doi: 10.1016/j.nbd.2023.106172. Epub 2023 May 29. Neurobiol Dis. 2023. PMID: 37257665 Free article. Review.

2

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.

El-Bazzal L, Rihan K, Bernard-Marissal N, Castro C, Chouery-Khoury E, Desvignes JP, Atkinson A, Bertaux K, Koussa S, Lévy N, Bartoli M, Mégarbané A, Jabbour R, Delague V. El-Bazzal L, et al. Hum Mol Genet. 2019 Jul 15;28(14):2378-2394. doi: 10.1093/hmg/ddz060. Hum Mol Genet. 2019. PMID: 31090908

3

VRK1 functional insufficiency due to alterations in protein stability or kinase activity of human VRK1 pathogenic variants implicated in neuromotor syndromes.

Martín-Doncel E, Rojas AM, Cantarero L, Lazo PA. Martín-Doncel E, et al. Sci Rep. 2019 Sep 16;9(1):13381. doi: 10.1038/s41598-019-49821-7. Sci Rep. 2019. PMID: 31527692 Free PMC article.

4

VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathy.

Marcos AT, Martín-Doncel E, Morejón-García P, Marcos-Alcalde I, Gómez-Puertas P, Segura-Puimedon M, Armengol L, Navarro-Pando JM, Lazo PA. Marcos AT, et al. Ann Clin Transl Neurol. 2020 May;7(5):808-818. doi: 10.1002/acn3.51050. Epub 2020 May 4. Ann Clin Transl Neurol. 2020. PMID: 32365420 Free PMC article.

5

Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study.

Sedghi M, Moslemi AR, Olive M, Etemadifar M, Ansari B, Nasiri J, Emrahi L, Mianesaz HR, Laing NG, Tajsharghi H. Sedghi M, et al. Ann Clin Transl Neurol. 2019 Nov;6(11):2197-2204. doi: 10.1002/acn3.50912. Epub 2019 Sep 27. Ann Clin Transl Neurol. 2019. PMID: 31560180 Free PMC article.

6

Molecular analysis and clinical diversity of distal hereditary motor neuropathy.

Liu X, Duan X, Zhang Y, Sun A, Fan D. Liu X, et al. Eur J Neurol. 2020 Jul;27(7):1319-1326. doi: 10.1111/ene.14260. Epub 2020 May 12. Eur J Neurol. 2020. PMID: 32298515

7

[Genetic distribution in Chinese patients with hereditary peripheral neuropathy].

Liu XX, Duan XH, Zhang S, Sun AP, Zhang YS, Fan DS. Liu XX, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2022 Oct 18;54(5):874-883. doi: 10.19723/j.issn.1671-167X.2022.05.015. Beijing Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 36241230 Free PMC article. Chinese.

8

VRK1 variants in two Portuguese unrelated patients with childhood-onset motor neuron disease.

Silva DP, Soeiro E Sá M, Silveira F, Pinto S, Gromicho M, Sousa AB, Leão M, De Carvalho M. Silva DP, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):291-295. doi: 10.1080/21678421.2020.1746343. Epub 2020 Apr 3. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32242460

9

ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.

Montecchiani C, Pedace L, Lo Giudice T, Casella A, Mearini M, Gaudiello F, Pedroso JL, Terracciano C, Caltagirone C, Massa R, St George-Hyslop PH, Barsottini OG, Kawarai T, Orlacchio A. Montecchiani C, et al. Brain. 2016 Jan;139(Pt 1):73-85. doi: 10.1093/brain/awv320. Epub 2015 Nov 10. Brain. 2016. PMID: 26556829 Free PMC article.

10

A novel VRK1 mutation associated with recessive distal hereditary motor neuropathy.

Feng SY, Li LY, Feng SM, Zou ZY. Feng SY, et al. Ann Clin Transl Neurol. 2018 Dec 3;6(2):401-405. doi: 10.1002/acn3.701. eCollection 2019 Feb. Ann Clin Transl Neurol. 2018. PMID: 30847374 Free PMC article.

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