347 related articles for article (PubMed ID: 10073277)
1. Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms.
Warner LE; Garcia CA; Lupski JR
Annu Rev Med; 1999; 50():263-75. PubMed ID: 10073277
[TBL] [Abstract][Full Text] [Related]
2. Inherited peripheral neuropathy.
Keller MP; Chance PF
Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. [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]
6. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular genetics of inherited peripheral neuropathies: who are the actors?
Meuleman J; Timmerman V; Nelis E; De Jonghe P
Acta Neurol Belg; 2000 Sep; 100(3):171-80. PubMed ID: 11098291
[TBL] [Abstract][Full Text] [Related]
9. Many facets of the peripheral myelin protein PMP22 in myelination and disease.
Naef R; Suter U
Microsc Res Tech; 1998 Jun; 41(5):359-71. PubMed ID: 9672419
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Actual nosology of polyneuropathies in childhood].
Férnandez-Alvarez E
Rev Neurol; 1996 Nov; 24(135):1382-4. PubMed ID: 8974741
[TBL] [Abstract][Full Text] [Related]
12. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
Verhamme C; Baas F
Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
[TBL] [Abstract][Full Text] [Related]
13. Clinical features and molecular genetics of hereditary peripheral neuropathies.
Kuhlenbäumer G; Young P; Hünermund G; Ringelstein B; Stögbauer F
J Neurol; 2002 Dec; 249(12):1629-50. PubMed ID: 12529785
[TBL] [Abstract][Full Text] [Related]
14. A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies.
Moszyńska I; Kabzińska D; Sinkiewicz-Darol E; Kochański A
Acta Biochim Pol; 2009; 56(4):627-30. PubMed ID: 19830275
[TBL] [Abstract][Full Text] [Related]
15. [Advances in the molecular genetics of the hereditary neuropathies].
Palau F; Cuesta A; Pedrola L
Rev Neurol; 2002 Aug 1-15; 35(3):246-53. PubMed ID: 12235587
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary neuropathy with liability to pressure palsies in childhood].
de las Cuevas I; Arteaga R; García A; Herranz JL
Rev Neurol; 2000 Jul 1-15; 31(1):38-41. PubMed ID: 10948581
[TBL] [Abstract][Full Text] [Related]
17. Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination.
Warner LE; Hilz MJ; Appel SH; Killian JM; Kolodry EH; Karpati G; Carpenter S; Watters GV; Wheeler C; Witt D; Bodell A; Nelis E; Van Broeckhoven C; Lupski JR
Neuron; 1996 Sep; 17(3):451-60. PubMed ID: 8816708
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.
Adlkofer K; Martini R; Aguzzi A; Zielasek J; Toyka KV; Suter U
Nat Genet; 1995 Nov; 11(3):274-80. PubMed ID: 7581450
[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]