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Journal Abstract Search

103 related items for PubMed ID: 7356409

  • 1. Dejerine-Sottas disease revisited.
    Satran R.
    Arch Neurol; 1980 Feb; 37(2):67-8. PubMed ID: 7356409
    [Abstract] [Full Text] [Related]

  • 2. 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; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 3. [Renaut's bodies and familial neuropathy of the Dejerine-Sottas type. Apropos of 2 anatomo-clinical cases].
    Pasquier B, Couderc P, Pasquier D.
    Sem Hop; 1987 Feb; 51(31-34):2103-7. PubMed ID: 52195
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  • 8. Subarachnoid block and enlargement of the spinal canal in hypertrophic neuritis.
    De León GA, Hodges FJ.
    J Neurol Sci; 1976 Jun; 28(2):139-46. PubMed ID: 1271079
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  • 9. Hypertrophic interstitial polyneuropathy in infancy. Clinical and pathologic features in two cases.
    Anderson RM, Dennett X, Hopkins IJ, Shield LK.
    J Pediatr; 1973 Apr; 82(4):619-24. PubMed ID: 4121461
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  • 10. Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy.
    Nara T, Akashi M, Nonaka I, Nakanishi Y, Hamano S, Ochiai Y, Tsuzura S.
    J Neurol Sci; 1995 Apr; 129(2):170-4. PubMed ID: 7608732
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  • 11. MR imaging of Dejerine-Sottas disease.
    Maki DD, Yousem DM, Corcoran C, Galetta SL.
    AJNR Am J Neuroradiol; 1999 Mar; 20(3):378-80. PubMed ID: 10219400
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  • 12. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].
    Jedrzejowska H, Drac H, Sawicka E.
    Neuropatol Pol; 1975 Mar; 13(1):93-106. PubMed ID: 1118064
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  • 13. Segmental demyelinization in Dejerine-Sottas disease: light, phase-contrast, and electron microscopic studies.
    Dyck PJ, Gomez MR.
    Mayo Clin Proc; 1968 Apr; 43(4):280-96. PubMed ID: 4304238
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  • 14. Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).
    Joosten E, Gabreëls F, Gabrèèls-Festen A, Vrensen G, Korten J, Notermans S.
    Acta Neuropathol; 1974 Feb 28; 27(2):105-18. PubMed ID: 4152255
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  • 15. [Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)--clinical features and the findings of nerve pathology].
    Tachi N, Hosoya S, Sasaki K, Watanabe M, Nagaoka M, Wakai S, Kameda K, Minami R.
    No To Hattatsu; 1988 May 28; 20(3):211-6. PubMed ID: 3164619
    [No Abstract] [Full Text] [Related]

  • 16. [Progressive asymmetrical peripheral neuropathy of both legs in a 64-year-old man].
    Kuntzer T, Talamon C, Said G.
    Rev Neurol (Paris); 1998 Nov 28; 154(11):789-94. PubMed ID: 9894299
    [No Abstract] [Full Text] [Related]

  • 17. An electron microscopic study of hypertrophic neuropathy of Dejerine and Sottas.
    Weller RO.
    J Neurol Neurosurg Psychiatry; 1967 Apr 28; 30(2):111-25. PubMed ID: 4291874
    [No Abstract] [Full Text] [Related]

  • 18. Chronic neuropathy presenting as a floppy infant with respiratory distress.
    Moss RB, Sriram S, Kelts KA, Forno LS, Lewiston NJ.
    Pediatrics; 1979 Oct 28; 64(4):459-64. PubMed ID: 492811
    [Abstract] [Full Text] [Related]

  • 19. [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy].
    Drac H.
    Neuropatol Pol; 1977 Oct 28; 15(1):1-16. PubMed ID: 840382
    [No Abstract] [Full Text] [Related]

  • 20. Hypertrophic neuropathy with spinal cord compression.
    Carlin L, Biller J, Challa V, Riela A.
    Surg Neurol; 1982 Oct 28; 18(4):237-40. PubMed ID: 7179080
    [Abstract] [Full Text] [Related]

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