453 related articles for article (PubMed ID: 9633821)
1. Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.
Silander K; Meretoja P; Juvonen V; Ignatius J; Pihko H; Saarinen A; Wallden T; Herrgård E; Aula P; Savontaus ML
Hum Mutat; 1998; 12(1):59-68. PubMed ID: 9633821
[TBL] [Abstract][Full Text] [Related]
2. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.
Mersiyanova IV; Ismailov SM; Polyakov AV; Dadali EL; Fedotov VP; Nelis E; Löfgren A; Timmerman V; van Broeckhoven C; Evgrafov OV
Hum Mutat; 2000; 15(4):340-7. PubMed ID: 10737979
[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. Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations.
Numakura C; Lin C; Ikegami T; Guldberg P; Hayasaka K
Hum Mutat; 2002 Nov; 20(5):392-8. PubMed ID: 12402337
[TBL] [Abstract][Full Text] [Related]
5. Mutation testing in Charcot-Marie-Tooth neuropathy.
Nicholson GA
Ann N Y Acad Sci; 1999 Sep; 883():383-8. PubMed ID: 10586262
[TBL] [Abstract][Full Text] [Related]
6. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.
Nelis E; Haites N; Van Broeckhoven C
Hum Mutat; 1999; 13(1):11-28. PubMed ID: 9888385
[TBL] [Abstract][Full Text] [Related]
7. Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.
Huehne K; Benes V; Thiel C; Kraus C; Kress W; Hoeltzenbein M; Ploner CJ; Kotzian J; Reis A; Rott HD; Rautenstrauss BW
Hum Mutat; 2003 Jan; 21(1):100. PubMed ID: 12497641
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
Bort S; Nelis E; Timmerman V; Sevilla T; Cruz-Martínez A; Martínez F; Millán JM; Arpa J; Vílchez JJ; Prieto F; Van Broeckhoven C; Palau F
Hum Genet; 1997 Jun; 99(6):746-54. PubMed ID: 9187667
[TBL] [Abstract][Full Text] [Related]
10. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.
Chance PF; Lupski JR
Baillieres Clin Neurol; 1994 Aug; 3(2):373-85. PubMed ID: 7952853
[TBL] [Abstract][Full Text] [Related]
11. Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.
Mostacciuolo ML; Righetti E; Zortea M; Bosello V; Schiavon F; Vallo L; Merlini L; Siciliano G; Fabrizi GM; Rizzuto N; Milani M; Baratta S; Taroni F
Hum Mutat; 2001; 18(1):32-41. PubMed ID: 11438991
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [PCR in the gene diagnosis of Charcot-Marie-Tooth disease].
Xiao J; Tang B; Xia J
Zhonghua Yi Xue Za Zhi; 2001 Feb; 81(3):138-41. PubMed ID: 11798863
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Inherited peripheral neuropathy.
Keller MP; Chance PF
Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
[TBL] [Abstract][Full Text] [Related]
16. [Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].
Hayasaka K
Rinsho Shinkeigaku; 1995 Dec; 35(12):1444-6. PubMed ID: 8752425
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.
Latour P; Blanquet F; Nelis E; Bonnebouche C; Chapon F; Diraison P; Ollagnon E; Dautigny A; Pham-Dinh D; Chazot G
Hum Mutat; 1995; 6(1):50-4. PubMed ID: 7550231
[TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
Resko P; Radvansky J; Odnogova Z; Baldovic M; Minarik G; Polakova H; Palffy R; Kadasi L
Gen Physiol Biophys; 2011 Dec; 30(4):379-88. PubMed ID: 22131320
[TBL] [Abstract][Full Text] [Related]
19. Mutations in the peripheral myelin protein zero and connexin32 genes detected by non-isotopic RNase cleavage assay and their phenotypes in Japanese patients with Charcot-Marie-Tooth disease.
Yoshihara T; Yamamoto M; Doyu M; Mis KI; Hattori N; Hasegawa Y; Mokuno K; Mitsuma T; Sobue G
Hum Mutat; 2000 Aug; 16(2):177-8. PubMed ID: 10923043
[TBL] [Abstract][Full Text] [Related]
20. Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1.
Numakura C; Lin C; Oka N; Akiguchi I; Hayasaka K
Ann Neurol; 2000 Jan; 47(1):101-3. PubMed ID: 10632107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]