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Journal Abstract Search

152 related items for PubMed ID: 18795595

  • 1. Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family.
    Zambelis T, Panas M, Kokotis P, Karadima G, Kararizou E, Karandreas N.
    Acta Neurol Belg; 2008 Jun; 108(2):44-7. PubMed ID: 18795595
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  • 2. 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
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  • 3. 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
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  • 5. 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
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  • 6. X-linked Charcot-Marie-Tooth disease: molecular analysis of interfamilial variability.
    Niewiadomski LA, Kelly TE.
    Am J Med Genet; 1996 Dec 11; 66(2):175-8. PubMed ID: 8958325
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  • 7. Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene.
    Bähr M, Andres F, Timmerman V, Nelis ME, Van Broeckhoven C, Dichgans J.
    J Neurol Neurosurg Psychiatry; 1999 Feb 11; 66(2):202-6. PubMed ID: 10071100
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  • 9. 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 11; 15(2):361-70. PubMed ID: 15006706
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  • 10. 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 15; 341(1-2):158-61. PubMed ID: 24768312
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  • 11. Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
    Beauvais K, Furby A, Latour P.
    Neuromuscul Disord; 2006 Jan 15; 16(1):14-8. PubMed ID: 16373087
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  • 12. Persistent CNS dysfunction in a boy with CMT1X.
    Siskind C, Feely SM, Bernes S, Shy ME, Garbern JY.
    J Neurol Sci; 2009 Apr 15; 279(1-2):109-13. PubMed ID: 19193385
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  • 13. 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 15; 251(2):222-3. PubMed ID: 14991359
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  • 15. 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 09; 7():19. PubMed ID: 17620124
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  • 16. 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 09; 25(8):1013-6. PubMed ID: 20472869
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  • 18. A distinct subgroup of chronic inflammatory demyelinating polyneuropathy with CNS demyelination and a favorable response to immunotherapy.
    Pineda AA, Ogata K, Osoegawa M, Murai H, Shigeto H, Yoshiura T, Tobimatsu S, Kira J.
    J Neurol Sci; 2007 Apr 15; 255(1-2):1-6. PubMed ID: 17306302
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  • 19. 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 15; 25(6):759-63. PubMed ID: 20382840
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