264 related articles for article (PubMed ID: 11231025)
1. Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2.
Gemignani F; Marbini A
J Neurol Sci; 2001 Feb; 184(1):1-9. PubMed ID: 11231025
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.
Georgiou DM; Zidar J; Korosec M; Middleton LT; Kyriakides T; Christodoulou K
Neurogenetics; 2002 Oct; 4(2):93-6. PubMed ID: 12481988
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genetic evaluation of inherited motor/sensory neuropathy.
Chance PF
Suppl Clin Neurophysiol; 2004; 57():228-42. PubMed ID: 16106622
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
8. Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.
De Jonghe P; Timmerman V; FitzPatrick D; Spoelders P; Martin JJ; Van Broeckhoven C
J Neurol Neurosurg Psychiatry; 1997 Jun; 62(6):570-3. PubMed ID: 9219740
[TBL] [Abstract][Full Text] [Related]
9. Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene.
Marrosu MG; Vaccargiu S; Marrosu G; Vannelli A; Cianchetti C; Muntoni F
Neurology; 1998 May; 50(5):1397-401. PubMed ID: 9595994
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
Berciano J; García A; Gallardo E; Peeters K; Pelayo-Negro AL; Álvarez-Paradelo S; Gazulla J; Martínez-Tames M; Infante J; Jordanova A
J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.
Tazir M; Hamadouche T; Nouioua S; Mathis S; Vallat JM
J Neurol Sci; 2014 Dec; 347(1-2):14-22. PubMed ID: 25454638
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.
Houlden H; Reilly MM
Neuromolecular Med; 2006; 8(1-2):43-62. PubMed ID: 16775366
[TBL] [Abstract][Full Text] [Related]
16. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
De Sandre-Giovannoli A; Chaouch M; Kozlov S; Vallat JM; Tazir M; Kassouri N; Szepetowski P; Hammadouche T; Vandenberghe A; Stewart CL; Grid D; Lévy N
Am J Hum Genet; 2002 Mar; 70(3):726-36. PubMed ID: 11799477
[TBL] [Abstract][Full Text] [Related]
17. Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A.
Saito M; Hayashi Y; Suzuki T; Tanaka H; Hozumi I; Tsuji S
Neurology; 1997 Dec; 49(6):1630-5. PubMed ID: 9409358
[TBL] [Abstract][Full Text] [Related]
18. MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.
Braathen GJ; Sand JC; Lobato A; Høyer H; Russell MB
BMC Med Genet; 2010 Mar; 11():48. PubMed ID: 20350294
[TBL] [Abstract][Full Text] [Related]
19. [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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
