274 related articles for article (PubMed ID: 25326399)
1. Intermediate Charcot-Marie-Tooth disease.
Liu L; Zhang R
Neurosci Bull; 2014 Dec; 30(6):999-1009. PubMed ID: 25326399
[TBL] [Abstract][Full Text] [Related]
2. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
Berciano J; García A; Gallardo E; Peeters K; Pelayo-Negro AL; Álvarez-Paradelo S; Gazulla J; Martínez-Tames M; Infante J; Jordanova A
J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294
[TBL] [Abstract][Full Text] [Related]
3. Genetic epidemiology of Charcot-Marie-Tooth disease.
Braathen GJ
Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
[TBL] [Abstract][Full Text] [Related]
4. Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
Miltenberger-Miltenyi G; Janecke AR; Wanschitz JV; Timmerman V; Windpassinger C; Auer-Grumbach M; Löscher WN
Arch Neurol; 2007 Jul; 64(7):966-70. PubMed ID: 17620486
[TBL] [Abstract][Full Text] [Related]
5. [Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].
Berciano J; Sevilla T; Casasnovas C; Sivera R; Vílchez JJ; Infante J; Ramón C; Pelayo-Negro AL; Illa I;
Neurologia; 2012 Apr; 27(3):169-78. PubMed ID: 21703725
[TBL] [Abstract][Full Text] [Related]
6. Intermediate forms of Charcot-Marie-Tooth neuropathy: a review.
Nicholson G; Myers S
Neuromolecular Med; 2006; 8(1-2):123-30. PubMed ID: 16775371
[TBL] [Abstract][Full Text] [Related]
7. Charcot-Marie-Tooth disease: frequency of genetic subtypes in a German neuromuscular center population.
Gess B; Schirmacher A; Boentert M; Young P
Neuromuscul Disord; 2013 Aug; 23(8):647-51. PubMed ID: 23743332
[TBL] [Abstract][Full Text] [Related]
8. Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies.
Østern R; Fagerheim T; Hjellnes H; Nygård B; Mellgren SI; Nilssen Ø
BMC Med Genet; 2013 Sep; 14():94. PubMed ID: 24053775
[TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic spectra of Charcot-Marie-Tooth disease in Chinese Han patients.
Sun B; Chen Z; Ling L; Yang F; Huang X
J Peripher Nerv Syst; 2017 Mar; 22(1):13-18. PubMed ID: 27862672
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic yield of targeted sequential and massive panel approaches for inherited neuropathies.
Padilha JPD; Brasil CS; Hoefel AML; Winckler PB; Donis KC; Brusius-Facchin AC; Saute JAM
Clin Genet; 2020 Aug; 98(2):185-190. PubMed ID: 32506583
[TBL] [Abstract][Full Text] [Related]
11. Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan.
Yoshimura A; Yuan JH; Hashiguchi A; Ando M; Higuchi Y; Nakamura T; Okamoto Y; Nakagawa M; Takashima H
J Neurol Neurosurg Psychiatry; 2019 Feb; 90(2):195-202. PubMed ID: 30257968
[TBL] [Abstract][Full Text] [Related]
12. Strategy for genetic testing in Charcot-Marie-disease.
Miller LJ; Saporta AS; Sottile SL; Siskind CE; Feely SM; Shy ME
Acta Myol; 2011 Oct; 30(2):109-16. PubMed ID: 22106713
[TBL] [Abstract][Full Text] [Related]
13. Charcot-Marie-Tooth disease with intermediate conduction velocities caused by a novel mutation in the MPZ gene.
Banchs I; Casasnovas C; Montero J; Volpini V; Martínez-Matos JA
Muscle Nerve; 2010 Aug; 42(2):184-8. PubMed ID: 20544920
[TBL] [Abstract][Full Text] [Related]
14. Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients.
Rudnik-Schöneborn S; Tölle D; Senderek J; Eggermann K; Elbracht M; Kornak U; von der Hagen M; Kirschner J; Leube B; Müller-Felber W; Schara U; von Au K; Wieczorek D; Bußmann C; Zerres K
Clin Genet; 2016 Jan; 89(1):34-43. PubMed ID: 25850958
[TBL] [Abstract][Full Text] [Related]
15. Mutational analysis of the 5' non-coding region of GJB1 in a Taiwanese cohort with Charcot-Marie-Tooth neuropathy.
Tsai PC; Chen CH; Liu AB; Chen YC; Soong BW; Lin KP; Yet SF; Lee YC
J Neurol Sci; 2013 Sep; 332(1-2):51-5. PubMed ID: 23827825
[TBL] [Abstract][Full Text] [Related]
16. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease.
Bergamin G; Boaretto F; Briani C; Pegoraro E; Cacciavillani M; Martinuzzi A; Muglia M; Vettori A; Vazza G; Mostacciuolo ML
Neuromolecular Med; 2014 Sep; 16(3):540-50. PubMed ID: 24819634
[TBL] [Abstract][Full Text] [Related]
18. Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.
Rouger H; LeGuern E; Birouk N; Gouider R; Tardieu S; Plassart E; Gugenheim M; Vallat JM; Louboutin JP; Bouche P; Agid Y; Brice A
Hum Mutat; 1997; 10(6):443-52. PubMed ID: 9401007
[TBL] [Abstract][Full Text] [Related]
19. Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis.
Benedetti S; Previtali SC; Coviello S; Scarlato M; Cerri F; Di Pierri E; Piantoni L; Spiga I; Fazio R; Riva N; Natali Sora MG; Dacci P; Malaguti MC; Munerati E; Grimaldi LM; Marrosu MG; De Pellegrin M; Ferrari M; Comi G; Quattrini A; Bolino A
Arch Neurol; 2010 Dec; 67(12):1498-505. PubMed ID: 21149811
[TBL] [Abstract][Full Text] [Related]
20. Genotype-phenotype characteristics of Vietnamese patients diagnosed with Charcot-Marie-Tooth disease.
Nguyen-Le TH; Do MD; Le LHG; Nhat QNN; Hoang NTT; Van Le T; Mai TP
Brain Behav; 2022 Sep; 12(9):e2744. PubMed ID: 35938991
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]