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 *

119 related articles for article (PubMed ID: 20382840)

  • 1. Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.
    Fusco C; Frattini D; Pisani F; Spaggiari F; Ferlini A; Della Giustina E
    J Child Neurol; 2010 Jun; 25(6):759-63. PubMed ID: 20382840
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transient leukoencephalopathy associated with X-linked Charcot-Marie-Tooth disease.
    Rosser T; Muir J; Panigrahy A; Baldwin EE; Boles RG
    J Child Neurol; 2010 Aug; 25(8):1013-6. PubMed ID: 20472869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. X-linked Charcot-Marie-Tooth disease caused by a novel point mutation in the connexin-32 gene.
    Ma W; Farrukh Nizam M; Grewal RP
    Neurol Sci; 2002 Oct; 23(4):195-7. PubMed ID: 12536289
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease.
    Isoardo G; Di Vito N; Nobile M; Benetton G; Fassio F
    Neurology; 2005 Nov; 65(10):1672-3. PubMed ID: 16301507
    [No Abstract]   [Full Text] [Related]  

  • 7. Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease.
    Braathen GJ; Sand JC; Bukholm G; Russell MB
    BMC Neurol; 2007 Jul; 7():19. PubMed ID: 17620124
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Persistent CNS dysfunction in a boy with CMT1X.
    Siskind C; Feely SM; Bernes S; Shy ME; Garbern JY
    J Neurol Sci; 2009 Apr; 279(1-2):109-13. PubMed ID: 19193385
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities.
    Murru MR; Vannelli A; Marrosu G; Cocco E; Corongiu D; Tranquilli S; Cherchi MV; Mura M; Barberini L; Mallarini G; Marrosu MG
    Neurol Sci; 2006 Apr; 27(1):18-23. PubMed ID: 16688595
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features.
    Karadima G; Panas M; Floroskufi P; Kalfakis N; Vassilopoulos D
    J Neurol; 2004 Feb; 251(2):222-3. PubMed ID: 14991359
    [No Abstract]   [Full Text] [Related]  

  • 11. Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation.
    Hanemann CO; Bergmann C; Senderek J; Zerres K; Sperfeld AD
    Arch Neurol; 2003 Apr; 60(4):605-9. PubMed ID: 12707076
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked Charcot-Marie-Tooth disease and connexin32.
    Fischbeck KH; Abel A; Lin GS; Scherer SS
    Ann N Y Acad Sci; 1999 Sep; 883():36-41. PubMed ID: 10586227
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.
    Paulson HL; Garbern JY; Hoban TF; Krajewski KM; Lewis RA; Fischbeck KH; Grossman RI; Lenkinski R; Kamholz JA; Shy ME
    Ann Neurol; 2002 Oct; 52(4):429-34. PubMed ID: 12325071
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.
    Sagnelli A; Piscosquito G; Chiapparini L; Ciano C; Salsano E; Saveri P; Milani M; Taroni F; Pareyson D
    J Peripher Nerv Syst; 2014 Jun; 19(2):183-6. PubMed ID: 24863494
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. New mutation of gap junction protein beta1 (GJB1) gene in X-linked hereditary motor and sensory neuropathy.
    Umehara F; Arimura Y; Osame M; Minato S; Nakahara K
    J Peripher Nerv Syst; 2006 Mar; 11(1):96-7. PubMed ID: 16519791
    [No Abstract]   [Full Text] [Related]  

  • 17. [Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease].
    Qiao XH; Li YX; Chang XZ; Luan XH; Chen B; Bu DF; Yuan Y
    Zhonghua Yi Xue Za Zhi; 2009 Dec; 89(47):3328-31. PubMed ID: 20193560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Connexin32 in the peripheral nervous system. Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease.
    Nicholson SM; Ressot C; Gomès D; D'Andrea P; Perea J; Duval N; Bruzzone R
    Ann N Y Acad Sci; 1999 Sep; 883():168-85. PubMed ID: 10586243
    [No Abstract]   [Full Text] [Related]  

  • 19. Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population.
    Casasnovas C; Banchs I; Corral J; Martínez-Matos JA; Volpini V
    Clin Genet; 2006 Dec; 70(6):516-23. PubMed ID: 17100997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X-linked Charcot-Marie-Tooth disease and connexin32.
    Ionasescu VV
    Cell Biol Int; 1998 Nov; 22(11-12):807-13. PubMed ID: 10873293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.