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Journal Abstract Search

154 related items for PubMed ID: 3472423

  • 1. Prevalence of hereditary motor and sensory neuropathy in Cantabria.
    Combarros O, Calleja J, Polo JM, Berciano J.
    Acta Neurol Scand; 1987 Jan; 75(1):9-12. PubMed ID: 3472423
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  • 2. Hereditary motor and sensory neuropathies in Swedish children. I. Prevalence and distribution by disability groups.
    Hagberg B, Westerberg B.
    Acta Paediatr Scand; 1983 May; 72(3):379-83. PubMed ID: 6576612
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  • 3. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)].
    Takashima H.
    Rinsho Shinkeigaku; 2014 May; 54(12):957-9. PubMed ID: 25672680
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  • 5. Hereditary sensory neuropathies.
    Houlden H, Blake J, Reilly MM.
    Curr Opin Neurol; 2004 Oct; 17(5):569-77. PubMed ID: 15367861
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  • 6. 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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  • 7. [Prevalence of peroneal muscular atrophy in Cantabria].
    Combarros O, Rebollo M, Calleja J, Berciano J.
    Rev Clin Esp; 1982 Sep 30; 166(6):281-4. PubMed ID: 7178569
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  • 8. 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
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  • 9. Hereditary motor and sensory neuropathies: a genetic and epidemiological study in the province of Turin, Italy.
    Chiò A, Tribolo A, Brignolio F, Leone M, Meineri P, Rosso MG, Mostert M, Schiffer D.
    Ital J Neurol Sci; 1987 Aug 01; 8(4):369-74. PubMed ID: 3500148
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  • 10. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
    Bird TD.
    Neurol Clin; 1989 Feb 01; 7(1):9-23. PubMed ID: 2646524
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  • 17. Hereditary motor and sensory neuropathies in Swedish children. III. De- and remyelinating type in 10 sporadic cases.
    Hagberg B, Westerberg B, Hagne I, Selldén U.
    Acta Paediatr Scand; 1983 Jul 01; 72(4):537-44. PubMed ID: 6578668
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  • 18. Genetic epidemiology of hereditary motor sensory neuropathies (type I).
    Mostacciuolo ML, Micaglio G, Fardin P, Danieli GA.
    Am J Med Genet; 1991 Jun 15; 39(4):479-81. PubMed ID: 1877629
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  • 19. 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 15; 56(10):1283-8. PubMed ID: 10520946
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  • 20. Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies.
    Bertorini T, Narayanaswami P, Rashed H.
    Neurologist; 2004 Nov 15; 10(6):327-37. PubMed ID: 15518599
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