205 related articles for article (PubMed ID: 14652447)
1. X-linked Charcot-Marie-Tooth disease with myokymia: report of a family.
Chakravarty A; Ghosh B; Sengupta S; Mukhopadhyay S
Neurol India; 2003 Sep; 51(3):385-7. PubMed ID: 14652447
[TBL] [Abstract][Full Text] [Related]
2. X-linked Charcot-Marie-Tooth disease: molecular analysis of interfamilial variability.
Niewiadomski LA; Kelly TE
Am J Med Genet; 1996 Dec; 66(2):175-8. PubMed ID: 8958325
[TBL] [Abstract][Full Text] [Related]
3. Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci.
Kochanski A; Kennerson M; Kawulak M; Ryniewicz B; Rowinska-Marcinska K; Walizada G; Nowakowski A; Hausmanowa-Petrusewicz I; Nicholson GA
Neurology; 2005 Feb; 64(3):533-5. PubMed ID: 15699389
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutation.
Verhelst HE; Lofgren A; Van Coster RN
Eur J Paediatr Neurol; 2000; 4(5):235-8. PubMed ID: 11030070
[TBL] [Abstract][Full Text] [Related]
6. Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation.
Srinivasan J; Leventer RJ; Kornberg AJ; Dahl HH; Ryan MM
Pediatr Neurol; 2008 Apr; 38(4):293-5. PubMed ID: 18358413
[TBL] [Abstract][Full Text] [Related]
7. A retrospective review of X-linked Charcot-Marie-Tooth disease in childhood.
Yiu EM; Geevasinga N; Nicholson GA; Fagan ER; Ryan MM; Ouvrier RA
Neurology; 2011 Feb; 76(5):461-6. PubMed ID: 21282593
[TBL] [Abstract][Full Text] [Related]
8. Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease.
Lance JW; Durke D; Pollard J
Clin Exp Neurol; 1979; 16():49-56. PubMed ID: 550956
[TBL] [Abstract][Full Text] [Related]
9. [Charcot-Marie-Tooth disease. Peroneal muscular atrophy].
Hagen T; Jensen D; Dietrichson P; Heiberg A
Tidsskr Nor Laegeforen; 1990 Oct; 110(24):3110-5. PubMed ID: 2237866
[TBL] [Abstract][Full Text] [Related]
10. X-linked Charcot-Marie-Tooth disease caused by a novel point mutation in the connexin-32 gene.
Ma W; Farrukh Nizam M; Grewal RP
Neurol Sci; 2002 Oct; 23(4):195-7. PubMed ID: 12536289
[TBL] [Abstract][Full Text] [Related]
11. [X-linked recessively inherited peroneal muscular atrophy].
Wang DS
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):139-40, 190. PubMed ID: 2591266
[TBL] [Abstract][Full Text] [Related]
12. [A family of early childhood-onset Charcot-Marie-Tooth disease type 2].
Hinuma Y; Aoki M; Takahashi T; Tateyama M; Nagai M; Yoshioka M; Itoyama Y
Rinsho Shinkeigaku; 2001 Jan; 41(1):64-7. PubMed ID: 11433771
[TBL] [Abstract][Full Text] [Related]
13. A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features.
Karadima G; Panas M; Floroskufi P; Kalfakis N; Vassilopoulos D
J Neurol; 2004 Feb; 251(2):222-3. PubMed ID: 14991359
[No Abstract] [Full Text] [Related]
14. X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study.
Ionasescu VV; Burns TL; Searby C; Ionasescu R
Muscle Nerve; 1988 Nov; 11(11):1154-6. PubMed ID: 3226432
[TBL] [Abstract][Full Text] [Related]
15. [Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome].
Chokri B; Salem M; Faycel H
Tunis Med; 2005 Sep; 83(9):547-55. PubMed ID: 16383201
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
Beauvais K; Furby A; Latour P
Neuromuscul Disord; 2006 Jan; 16(1):14-8. PubMed ID: 16373087
[TBL] [Abstract][Full Text] [Related]
18. Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study.
Micaglio G; Fardin P; Battilana M; Lombardi A; Mostacciuolo ML; Danieli GA; Angelini C
Adv Neurol; 1988; 48():209-19. PubMed ID: 3334783
[No Abstract] [Full Text] [Related]
19. Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease.
Braathen GJ; Sand JC; Bukholm G; Russell MB
BMC Neurol; 2007 Jul; 7():19. PubMed ID: 17620124
[TBL] [Abstract][Full Text] [Related]
20. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]