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PUBMED FOR HANDHELDS

Journal Abstract Search


154 related items for PubMed ID: 7224445

  • 21.
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  • 23. Quantitation of Meissner's corpuscles in hereditary neurologic disorders. Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia.
    Dyck PJ, Winkelmann RK, Bolton CF.
    Neurology; 1966 Jan; 16(1):10-7. PubMed ID: 5948001
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  • 29. [Charcot-Marie neural amyotrophy (review)].
    Savchenko IuN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Jan; 84(11):1718-22. PubMed ID: 6098115
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  • 30. Endoneurial space and its constituents in the sural nerve of patients with neuropathy.
    Behse F, Buchthal F, Carlsen F, Knappeis GG.
    Brain; 1974 Dec; 97(4):773-84. PubMed ID: 4373123
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  • 31. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients].
    Freitas MR, Nascimento OJ, Chimelli L, de Freitas GR.
    Arq Neuropsiquiatr; 1995 Sep; 53(3-B):560-9. PubMed ID: 8585811
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  • 35. Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves.
    Behse F, Buchthal F.
    Brain; 1977 Mar; 100 Pt 1():67-85. PubMed ID: 861716
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  • 36. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
    Thiam A, Sene FD, Ndao AK, Ndiaye M, Ndiaye IP.
    Dakar Med; 2002 Mar; 47(2):182-7. PubMed ID: 15776672
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  • 37. Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.
    Salisachs P.
    J Neurol Neurosurg Psychiatry; 1982 Dec; 45(12):1085-91. PubMed ID: 6186770
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  • 38. Data on three of the original patients of Roussy and Levy (1926).
    Salisachs P, Findley LJ, Codina M, La Torre P, Martinez-Lage JM.
    Muscle Nerve; 1982 Oct; 5(8):663-4. PubMed ID: 7155179
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  • 39. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 40. [Neurophysiological, histological and chromosome study of Charcot-Marie-Tooth disease].
    Messina C, Fiorillo A, Caliri F.
    Acta Neurol (Napoli); 1968 Jan; 23(1):21-33. PubMed ID: 5739560
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