These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies]. Sevilla T Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. 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]
11. 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]
13. Charcot-Marie-Tooth disease and related peripheral neuropathies. De Jonghe P; Timmerman V; Nelis E; Martin JJ; Van Broeckhoven C J Peripher Nerv Syst; 1997; 2(4):370-87. PubMed ID: 10975746 [TBL] [Abstract][Full Text] [Related]
14. Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A. Roa BB; Garcia CA; Pentao L; Killian JM; Trask BJ; Suter U; Snipes GJ; Ortiz-Lopez R; Shooter EM; Patel PI; Lupski JR Nat Genet; 1993 Oct; 5(2):189-94. PubMed ID: 8252046 [TBL] [Abstract][Full Text] [Related]
15. 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]
17. 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]
18. 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]
19. 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]
20. 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] [Next] [New Search]