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Journal Abstract Search

137 related items for PubMed ID: 3470161

  • 1. A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot-Marie-Tooth disease.
    Ruiz C, Rivas F, Ramírez-Casillas G, Vázquez-Santana R, Mendoza-Chalita B, Feria-Velasco A, Tapia-Arizmendi G, Cantú JM.
    Clin Genet; 1987 Feb; 31(2):109-13. PubMed ID: 3470161
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  • 2. Evidence for linkage of type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ, Thomas PK, Contreras M, Armitage S, Schwarz G, Sedgwick EM.
    Ann Hum Genet; 1982 Jan 01; 46(1):25-7. PubMed ID: 6954871
    [No Abstract] [Full Text] [Related]

  • 3. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb 01; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 4. Prevalence of hereditary motor and sensory neuropathy in Cantabria.
    Combarros O, Calleja J, Polo JM, Berciano J.
    Acta Neurol Scand; 1987 Jan 01; 75(1):9-12. PubMed ID: 3472423
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  • 7. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.
    Bellone E, Rodolico C, Toscano A, Di Maria E, Cassandrini D, Pizzuti A, Pigullo S, Mazzeo A, Macaione V, Girlanda P, Vita G, Ajmar F, Mandich P.
    Neuromuscul Disord; 2002 Mar 01; 12(3):286-91. PubMed ID: 11801401
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  • 8. Genetic heterogeneity of hereditary motor and sensory neuropathy type VI.
    Ippel EF, Wittebol-Post D, Jennekens FG, Bijlsma JB.
    J Child Neurol; 1995 Nov 01; 10(6):459-63. PubMed ID: 8576556
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  • 10. Hereditary sensory neuropathies.
    Houlden H, Blake J, Reilly MM.
    Curr Opin Neurol; 2004 Oct 01; 17(5):569-77. PubMed ID: 15367861
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  • 11. Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl.
    Danon MJ, Sarpel G, Manaligod JR.
    Arch Neurol; 1980 Feb 01; 37(2):123-7. PubMed ID: 7356407
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  • 12. [Hereditary sensory and motor neuropathy and hereditary sensory and autonomic neuropathies: recent advances].
    Stojkovic T.
    Rev Neurol (Paris); 2011 Dec 01; 167(12):948-50. PubMed ID: 22100327
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  • 14. Emerging pathways for hereditary axonopathies.
    Züchner S, Vance JM.
    J Mol Med (Berl); 2005 Dec 01; 83(12):935-43. PubMed ID: 16133422
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  • 15. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR.
    Afr J Med Med Sci; 1976 Dec 01; 5(4):269-72. PubMed ID: 829740
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  • 16. Recent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2.
    Ajroud-Driss S, Deng HX, Siddique T.
    Curr Neurol Neurosci Rep; 2011 Jun 01; 11(3):262-73. PubMed ID: 21327736
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  • 17. Myotonic dystrophy associated with hereditary motor and sensory neuropathy.
    Spaans F, Jennekens FG, Mirandolle JF, Bijlsma JB, de Gast GC.
    Brain; 1986 Dec 01; 109 ( Pt 6)():1149-68. PubMed ID: 3466660
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  • 18. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).
    Chan CK, Mohsenin V, Loke J, Virgulto J, Sipski ML, Ferranti R.
    Chest; 1987 Apr 01; 91(4):567-70. PubMed ID: 3829750
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  • 20. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C, Baas F.
    Ned Tijdschr Geneeskd; 2005 Jul 02; 149(27):1505-9. PubMed ID: 16032995
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