195 related articles for article (PubMed ID: 1733853)
1. Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.
Hentati A; Lamy C; Melki J; Zuber M; Munnich A; de Recondo J
Genomics; 1992 Jan; 12(1):155-7. PubMed ID: 1733853
[TBL] [Abstract][Full Text] [Related]
2. Genetic evaluation of inherited motor/sensory neuropathy.
Chance PF
Suppl Clin Neurophysiol; 2004; 57():228-42. PubMed ID: 16106622
[TBL] [Abstract][Full Text] [Related]
3. Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17.
McAlpine PJ; Feasby TE; Hahn AF; Komarnicki L; James S; Guy C; Dixon M; Qayyum S; Wright J; Coopland G
Genomics; 1990 Jul; 7(3):408-15. PubMed ID: 2365358
[TBL] [Abstract][Full Text] [Related]
4. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.
Kwon JM; Elliott JL; Yee WC; Ivanovich J; Scavarda NJ; Moolsintong PJ; Goodfellow PJ
Am J Hum Genet; 1995 Oct; 57(4):853-8. PubMed ID: 7573046
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Charcot-Marie-Tooth disease and related inherited neuropathies.
Murakami T; Garcia CA; Reiter LT; Lupski JR
Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346
[TBL] [Abstract][Full Text] [Related]
7. Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus.
Chance PF; Matsunami N; Lensch W; Smith B; Bird TD
Neurology; 1992 Oct; 42(10):2037-41. PubMed ID: 1407588
[TBL] [Abstract][Full Text] [Related]
8. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.
De Jonghe P; Timmerman V; Nelis E; De Vriendt E; Löfgren A; Ceuterick C; Martin JJ; Van Broeckhoven C
Arch Neurol; 1999 Oct; 56(10):1283-8. PubMed ID: 10520946
[TBL] [Abstract][Full Text] [Related]
9. Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2.
Yoshioka R; Dyck PJ; Chance PF
Neurology; 1996 Feb; 46(2):569-71. PubMed ID: 8614538
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.
Chance PF; Fischbeck KH
Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745
[TBL] [Abstract][Full Text] [Related]
11. A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.
Mersiyanova IV; Perepelov AV; Polyakov AV; Sitnikov VF; Dadali EL; Oparin RB; Petrin AN; Evgrafov OV
Am J Hum Genet; 2000 Jul; 67(1):37-46. PubMed ID: 10841809
[TBL] [Abstract][Full Text] [Related]
12. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
Tang BS; Luo W; Xia K; Xiao JF; Jiang H; Shen L; Tang JG; Zhao GH; Cai F; Pan Q; Dai HP; Yang QD; Xia JH; Evgrafov OV
Hum Genet; 2004 May; 114(6):527-33. PubMed ID: 15021985
[TBL] [Abstract][Full Text] [Related]
13. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.
Ben Othmane K; Middleton LT; Loprest LJ; Wilkinson KM; Lennon F; Rozear MP; Stajich JM; Gaskell PC; Roses AD; Pericak-Vance MA
Genomics; 1993 Aug; 17(2):370-5. PubMed ID: 8406488
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A.
Lupski JR; Garcia CA
Brain Pathol; 1992 Oct; 2(4):337-49. PubMed ID: 1341967
[TBL] [Abstract][Full Text] [Related]
15. [Genetics of peripheral neuropathies and hereditary ataxias].
Palau F; Sevilla T
Neurologia; 1995 Dec; 10 Suppl 1():32-43. PubMed ID: 8838557
[TBL] [Abstract][Full Text] [Related]
16. Inherited peripheral neuropathy.
Keller MP; Chance PF
Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
[TBL] [Abstract][Full Text] [Related]
17. Molecular basis of hereditary neuropathies.
Chance PF
Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007
[TBL] [Abstract][Full Text] [Related]
18. Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17.
Middleton-Price HR; Harding AE; Monteiro C; Berciano J; Malcolm S
Am J Hum Genet; 1990 Jan; 46(1):92-4. PubMed ID: 2294757
[TBL] [Abstract][Full Text] [Related]
19. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M
Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969
[TBL] [Abstract][Full Text] [Related]
20. A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.
Nicolaou P; Cianchetti C; Minaidou A; Marrosu G; Zamba-Papanicolaou E; Middleton L; Christodoulou K
Eur J Hum Genet; 2013 Feb; 21(2):190-4. PubMed ID: 22781092
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]