188 related articles for article (PubMed ID: 29710024)
1. [Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with heterozygote mutation of GJB1 gene: case report of a female patient].
Takemaru M; Shimoe Y; Sato K; Hashiguchi A; Takashima H; Kuriyama M
Rinsho Shinkeigaku; 2018 May; 58(5):302-307. PubMed ID: 29710024
[TBL] [Abstract][Full Text] [Related]
2. Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation.
Hanemann CO; Bergmann C; Senderek J; Zerres K; Sperfeld AD
Arch Neurol; 2003 Apr; 60(4):605-9. PubMed ID: 12707076
[TBL] [Abstract][Full Text] [Related]
3. X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.
Sagnelli A; Piscosquito G; Chiapparini L; Ciano C; Salsano E; Saveri P; Milani M; Taroni F; Pareyson D
J Peripher Nerv Syst; 2014 Jun; 19(2):183-6. PubMed ID: 24863494
[TBL] [Abstract][Full Text] [Related]
4. [Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review].
Zhang HH; Gao LG; Wang JM; Gao ZJ; Jiang YW; Wang S; Xiong H; Chang XZ; Wu Y
Zhonghua Er Ke Za Zhi; 2013 Nov; 51(11):813-8. PubMed ID: 24484554
[TBL] [Abstract][Full Text] [Related]
5. Spatial Fluctuation of Central Nervous System Lesions in X-linked Charcot-Marie-Tooth Disease with a Novel GJB1 Mutation.
Yoshimoto Y; Yoshimoto S; Kakiuchi K; Miyagawa R; Ota S; Hosokawa T; Ishida S; Higuchi Y; Hashiguchi A; Takashima H; Arawaka S
Intern Med; 2024 Feb; 63(4):571-576. PubMed ID: 37407465
[TBL] [Abstract][Full Text] [Related]
6. Recurrent episodes of reversible posterior leukoencephalopathy in three Chinese families with GJB1 mutations in X-linked Charcot-Marie-tooth type 1 disease: cases report.
Liang Y; Liu J; Cheng D; Wu Y; Mo L; Huang W
BMC Neurol; 2019 Dec; 19(1):325. PubMed ID: 31842800
[TBL] [Abstract][Full Text] [Related]
7. Recurrent central nervous system white matter changes in charcot-Marie-tooth type X disease.
McKinney JL; De Los Reyes EC; Lo WD; Flanigan KM
Muscle Nerve; 2014 Mar; 49(3):451-4. PubMed ID: 24170412
[TBL] [Abstract][Full Text] [Related]
8. [Charcot-Marie-Tooth disease showing transient central nervous system lesions after a large amount of alcohol intake: A case report].
Shimizu C; Kasahara H; Furuta N; Shibata M; Nagashima K; Hashiguchi A; Takashima H; Ikeda Y
Rinsho Shinkeigaku; 2018 Aug; 58(8):479-484. PubMed ID: 30068806
[TBL] [Abstract][Full Text] [Related]
9. X-linked Charcot-Marie-Tooth Disease Presenting with Stuttering Stroke-like Symptoms.
Hardy DI; Licht DJ; Vossough A; Kirschen MP
Neuropediatrics; 2019 Oct; 50(5):304-307. PubMed ID: 31220874
[TBL] [Abstract][Full Text] [Related]
10. Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report.
Zhao Y; Xie Y; Zhu X; Wang H; Li Y; Li J
BMC Neurol; 2014 Aug; 14():156. PubMed ID: 25086786
[TBL] [Abstract][Full Text] [Related]
11. Transient leukoencephalopathy associated with X-linked Charcot-Marie-Tooth disease.
Rosser T; Muir J; Panigrahy A; Baldwin EE; Boles RG
J Child Neurol; 2010 Aug; 25(8):1013-6. PubMed ID: 20472869
[TBL] [Abstract][Full Text] [Related]
12. X-linked Charcot-Marie-Tooth disease with GJB1 mutation presenting as acute disseminated encephalomyelitis-like illness: A case report.
Kim JK; Han SA; Kim SJ
Medicine (Baltimore); 2017 Dec; 96(49):e9176. PubMed ID: 29245364
[TBL] [Abstract][Full Text] [Related]
13. Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patient.
Martikainen MH; Majamaa K
Neuromuscul Disord; 2013 Nov; 23(11):899-901. PubMed ID: 23838279
[TBL] [Abstract][Full Text] [Related]
14. X-linked Charcot-Marie-Tooth disease: phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene.
Vondracek P; Seeman P; Hermanova M; Fajkusova L
Muscle Nerve; 2005 Feb; 31(2):252-5. PubMed ID: 15468313
[TBL] [Abstract][Full Text] [Related]
15. The central nervous system phenotype of X-linked Charcot-Marie-Tooth disease: a transient disorder of children and young adults.
Al-Mateen M; Craig AK; Chance PF
J Child Neurol; 2014 Mar; 29(3):342-8. PubMed ID: 23400245
[TBL] [Abstract][Full Text] [Related]
16. Genetic and phenotypic profile of 112 patients with X-linked Charcot-Marie-Tooth disease type 1.
Yuan JH; Sakiyama Y; Hashiguchi A; Ando M; Okamoto Y; Yoshimura A; Higuchi Y; Takashima H
Eur J Neurol; 2018 Dec; 25(12):1454-1461. PubMed ID: 29998508
[TBL] [Abstract][Full Text] [Related]
17. A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot-Marie-Tooth disease.
Sakaguchi H; Yamashita S; Miura A; Hirahara T; Kimura E; Maeda Y; Terasaki T; Hirano T; Uchino M
J Neurol; 2011 Feb; 258(2):284-90. PubMed ID: 20857133
[TBL] [Abstract][Full Text] [Related]
18. Novel gap junction protein beta-1 gene mutation associated with a stroke-like syndrome and central nervous system involvement in patients with X-linked Charcot-Marie-Tooth Type 1: A case report and literature review.
Hu G; Zhang L; Zhang M; Yang C; Nie X; Xiang F; Chen L; Dong Z; Yu S
Clin Neurol Neurosurg; 2019 May; 180():68-73. PubMed ID: 30952033
[TBL] [Abstract][Full Text] [Related]
19. Diffusion tensor imaging and magnetic resonance spectroscopy of transient cerebral white matter lesions in X-linked Charcot-Marie-Tooth disease.
Sato K; Kubo S; Fujii H; Okamoto M; Takahashi K; Takamatsu K; Tanaka A; Kuriyama M
J Neurol Sci; 2012 May; 316(1-2):178-80. PubMed ID: 22341131
[TBL] [Abstract][Full Text] [Related]
20. GJB1 mutations c.212T>G and c.311A>C induce apoptosis and inwardly rectifying potassium current changes in X-linked Charcot-Marie-Tooth type 1.
Guo H; Liu Y; Gu J; Luo J; Ma Y; Xiao F
Biochem Biophys Res Commun; 2021 Dec; 582():8-15. PubMed ID: 34678594
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
