161 related articles for article (PubMed ID: 12910991)
1. [Charcot-Marie-Tooth disease: an overview].
Kanda T
No To Shinkei; 2003 Jul; 55(7):576-86. PubMed ID: 12910991
[No Abstract] [Full Text] [Related]
2. Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.
Meggouh F; de Visser M; Arts WF; De Coo RI; van Schaik IN; Baas F
Ann Neurol; 2005 Apr; 57(4):589-91. PubMed ID: 15786462
[TBL] [Abstract][Full Text] [Related]
3. Congenital pes cavus in a Charcot-Marie-tooth disease type 1A newborn.
Fusco C; Frattini D; Scarano A; Giustina ED
Pediatr Neurol; 2009 Jun; 40(6):461-4. PubMed ID: 19433282
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.
Park HK; Kim BJ; Sung DH; Ki CS; Kim JW
Clin Genet; 2006 Sep; 70(3):253-6. PubMed ID: 16922730
[No Abstract] [Full Text] [Related]
5. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
6. Introduction to the Third International Symposium on Charcot-Marie-Tooth disorders.
Shy ME; Kamholz J; Lovelace RE
Ann N Y Acad Sci; 1999 Sep; 883():xiii-xviii. PubMed ID: 10586222
[No Abstract] [Full Text] [Related]
7. De novo Ser72Leu mutation in the peripheral myelin protein 22 in two Polish patients with a severe form of Charcot-Marie-Tooth disease.
Kochański A; Kabzińska D
Acta Biochim Pol; 2004; 51(4):1047-50. PubMed ID: 15625576
[TBL] [Abstract][Full Text] [Related]
8. Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies).
Postelmans JT; Stokroos RJ
J Laryngol Otol; 2006 Jun; 120(6):508-10. PubMed ID: 16772060
[TBL] [Abstract][Full Text] [Related]
9. The dominantly inherited motor and sensory neuropathies: clinical and molecular advances.
Nicholson GA
Muscle Nerve; 2006 May; 33(5):589-97. PubMed ID: 16392117
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins.
Harding AE
Brain; 1995 Jun; 118 ( Pt 3)():809-18. PubMed ID: 7541290
[TBL] [Abstract][Full Text] [Related]
12. Alterations in nodes of Ranvier and Schmidt-Lanterman incisures in Charcot-Marie-Tooth neuropathies.
Sahenk Z; Mendell JR
Ann N Y Acad Sci; 1999 Sep; 883():508-12. PubMed ID: 10586286
[No Abstract] [Full Text] [Related]
13. [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]
14. Novel human pathological mutations. Gene symbol: PMP22. Disease: Charcot-Marie-Tooth disease 1.
Rautenstrauss B; Huehne K
Hum Genet; 2007 Dec; 122(5):556. PubMed ID: 18383612
[No Abstract] [Full Text] [Related]
15. A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.
Joo IS; Ki CS; Joo SY; Huh K; Kim JW
Neuromuscul Disord; 2004 May; 14(5):325-8. PubMed ID: 15099592
[TBL] [Abstract][Full Text] [Related]
16. Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene.
Kochański A; Kabzińska D; Drac H; Ryniewicz B; Rowińska-Marcińska K; Hausmanowa-Petrusewicz I
Eur J Paediatr Neurol; 2004; 8(4):221-4. PubMed ID: 15261887
[TBL] [Abstract][Full Text] [Related]
17. Novel human pathological mutations. Gene symbol: PMP22. Disease: Charcot-Marie-Tooth syndrome type 1A.
Rautenstrauss B; Huehne K; Thiel C; Kraus C
Hum Genet; 2007 Dec; 122(5):545. PubMed ID: 18380017
[No Abstract] [Full Text] [Related]
18. [Molecular pathogenesis of hereditary motor and sensory neuropathy].
Kotruchow K; Kabzińska D; Karpińska K; Kochański A
Postepy Biochem; 2011; 57(3):283-93. PubMed ID: 22235654
[TBL] [Abstract][Full Text] [Related]
19. [Pathophysiology and new treatment for hereditary neuropathy].
Nodera H; Kaji R
No To Shinkei; 2004 Sep; 56(9):761-70. PubMed ID: 15552865
[No Abstract] [Full Text] [Related]
20. Charcot-Marie-Tooth disease: inherited neuropathies revisited.
Matiasek K; Drögemüller C
Vet J; 2011 Jun; 188(3):254-5. PubMed ID: 21459024
[No Abstract] [Full Text] [Related]
[Next] [New Search]
