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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 10639603)

  • 1. The challenge of CMTX and connexin 32 mutations.
    Lewis RA
    Muscle Nerve; 2000 Feb; 23(2):147-9. PubMed ID: 10639603
    [No Abstract]   [Full Text] [Related]  

  • 2. Efficient neurophysiologic selection of X-linked Charcot-Marie-Tooth families: ten novel mutations.
    Nicholson GA; Yeung L; Corbett A
    Neurology; 1998 Nov; 51(5):1412-6. PubMed ID: 9818870
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease.
    Dubourg O; Tardieu S; Birouk N; Gouider R; Léger JM; Maisonobe T; Brice A; Bouche P; LeGuern E
    Brain; 2001 Oct; 124(Pt 10):1958-67. PubMed ID: 11571214
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
    Birouk N; LeGuern E; Maisonobe T; Rouger H; Gouider R; Tardieu S; Gugenheim M; Routon MC; Léger JM; Agid Y; Brice A; Bouche P
    Neurology; 1998 Apr; 50(4):1074-82. PubMed ID: 9566397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Review of X-linked Charcot-Marie-Tooth Disease.
    Wang Y; Yin F
    J Child Neurol; 2016 May; 31(6):761-72. PubMed ID: 26385972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease.
    Hahn AF; Bolton CF; White CM; Brown WF; Tuuha SE; Tan CC; Ainsworth PJ
    Ann N Y Acad Sci; 1999 Sep; 883():366-82. PubMed ID: 10586261
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MRI findings in X-linked Charcot-Marie-Tooth disease associated with a novel connexin 32 mutation.
    U-King-Im JM; Yiu E; Donner EJ; Shroff M
    Clin Radiol; 2011 May; 66(5):471-4. PubMed ID: 21300330
    [No Abstract]   [Full Text] [Related]  

  • 8. Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.
    Lee MJ; Nelson I; Houlden H; Sweeney MG; Hilton-Jones D; Blake J; Wood NW; Reilly MM
    J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):304-6. PubMed ID: 12185164
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Connexin mutations in X-linked Charcot-Marie-Tooth disease.
    Bergoffen J; Scherer SS; Wang S; Scott MO; Bone LJ; Paul DL; Chen K; Lensch MW; Chance PF; Fischbeck KH
    Science; 1993 Dec; 262(5142):2039-42. PubMed ID: 8266101
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Corticospinal tract MRI hyperintensity in X-linked Charcot-Marie-Tooth Disease.
    Kassubek J; Bretschneider V; Sperfeld AD
    J Clin Neurosci; 2005 Jun; 12(5):588-9. PubMed ID: 16051098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female.
    Lin GS; Glass JD; Shumas S; Scherer SS; Fischbeck KH
    Ann N Y Acad Sci; 1999 Sep; 883():481-4. PubMed ID: 10586279
    [No Abstract]   [Full Text] [Related]  

  • 12. New mutations in the X-linked form of Charcot-Marie-Tooth disease.
    Latour P; Fabreguette A; Ressot C; Blanquet-Grossard F; Antoine JC; Calvas P; Chapon F; Corbillon E; Ollagnon E; Sturtz F; Boucherat M; Chazot G; Dautigny A; Pham-Dinh D; Vandenberghe A
    Eur Neurol; 1997; 37(1):38-42. PubMed ID: 9018031
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and electrophysiological studies of a family with probable X-linked dominant Charcot-Marie-Tooth neuropathy and ptosis.
    Wu T; Wang HL; Chu CC; Yu JM; Chen JY; Huang CC
    Chang Gung Med J; 2004 Jul; 27(7):489-500. PubMed ID: 15508871
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.
    Wang HL; Chang WT; Yeh TH; Wu T; Chen MS; Wu CY
    Neurobiol Dis; 2004 Mar; 15(2):361-70. PubMed ID: 15006706
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.
    Rouger H; LeGuern E; Birouk N; Gouider R; Tardieu S; Plassart E; Gugenheim M; Vallat JM; Louboutin JP; Bouche P; Agid Y; Brice A
    Hum Mutat; 1997; 10(6):443-52. PubMed ID: 9401007
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene.
    Ainsworth PJ; Bolton CF; Murphy BC; Stuart JA; Hahn AF
    Hum Genet; 1998 Aug; 103(2):242-4. PubMed ID: 9760211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease. Phenotypic variability and central nervous system involvement.
    Karadima G; Koutsis G; Raftopoulou M; Floroskufi P; Karletidi KM; Panas M
    J Neurol Sci; 2014 Jun; 341(1-2):158-61. PubMed ID: 24768312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A new mutation in the connexin 32 gene was found in Charcot- Marie-Tooth disease in Chinese patients].
    Da Y; Shen D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):316-8. PubMed ID: 11024208
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A point mutation in codon 3 of connexin-32 is associated with X-linked Charcot-Marie-Tooth neuropathy.
    Gupta S; Benstead T; Neumann P; Guernsey D
    Hum Mutat; 1996; 8(4):375-6. PubMed ID: 8956046
    [No Abstract]   [Full Text] [Related]  

  • 20. [Charcot-Marie Tooth type X (CMTX) disease: clinical and genetic characteristics of eleven patients].
    Kochański A; Ryniewicz B; Jedrzejowska H; Kabzińska D
    Neurol Neurochir Pol; 2002; 36(6):1087-94. PubMed ID: 12715686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.