These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


156 related items for PubMed ID: 6830105

  • 1. [Primary hypertrophic neuropathy in children. Apropos of a familial case].
    Talon P, Mair W, Beyer P.
    Ann Pediatr (Paris); 1983 Jan; 30(1):45-50. PubMed ID: 6830105
    [No Abstract] [Full Text] [Related]

  • 2. [Familial fibula amyotrophies of neurogenic origin].
    Vallat JM, Vital C.
    Cah Med; 1971 Jun 30; 12(10):803-15. PubMed ID: 4107838
    [No Abstract] [Full Text] [Related]

  • 3. A brief review of inherited hypertrophic neuropathy.
    Dyck PJ.
    Birth Defects Orig Artic Ser; 1971 Feb 30; 7(2):66-71. PubMed ID: 4950914
    [No Abstract] [Full Text] [Related]

  • 4. [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; 1971 Feb 30; 51(31-34):2103-7. PubMed ID: 52195
    [Abstract] [Full Text] [Related]

  • 5. [Delerium patterns in Déjerine-Sottas disease].
    Barcia D, Muñóz R.
    Actas Luso Esp Neurol Psiquiatr Cienc Afines; 1980 Feb 30; 8(5):337-46. PubMed ID: 7457222
    [No Abstract] [Full Text] [Related]

  • 6. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].
    Jedrzejowska H, Drac H, Sawicka E.
    Neuropatol Pol; 1975 Feb 30; 13(1):93-106. PubMed ID: 1118064
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)].
    Sadaba Garay F, Franco Vicario R, Miguel de la Villa F, Ibarmia Lahuerta J, Bustamante Murga V.
    Med Clin (Barc); 1980 Oct 10; 75(6):240-6. PubMed ID: 7421358
    [Abstract] [Full Text] [Related]

  • 9. [Familial brachial amyotrophic neuritis. Study of 2 families].
    Warot P, Petit H, Nuyts JP, Meignie S.
    Rev Neurol (Paris); 1973 Apr 10; 128(4):281-8. PubMed ID: 4774914
    [No Abstract] [Full Text] [Related]

  • 10. Hereditary hypertrophic neuropathy with facial and trigeminal involvement. Report of a case and comments on its possible identity with Hellsing syndrome.
    Kalyanaraman K, Smith BH, Schlagenhauff RE.
    Arch Neurol; 1974 Jul 10; 31(1):15-7. PubMed ID: 4834537
    [No Abstract] [Full Text] [Related]

  • 11. [Cumulative familial incidence of Kugelberg-Welander disease].
    Nemes A, Károly E, Csenkér E, Pintér S.
    Orv Hetil; 1986 Nov 09; 127(45):2735-9. PubMed ID: 3796971
    [No Abstract] [Full Text] [Related]

  • 12. Endoneurial space and its constituents in the sural nerve of patients with neuropathy.
    Behse F, Buchthal F, Carlsen F, Knappeis GG.
    Brain; 1974 Dec 09; 97(4):773-84. PubMed ID: 4373123
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. [Case of Déjerine-Sottas disease with schizophrenic symptoms].
    Nakao T, Okuma T, Matsushima Y, Takahashi K, Nagami M.
    Rinsho Shinkeigaku; 1972 Mar 09; 12(3):149-57. PubMed ID: 4674763
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Onion bulb neuropathy in the trembler mouse: a model of hypertrophic interstitial neuropathy (Dejerine-Sottas) in man.
    Ayers MM, Anderson RM.
    Acta Neuropathol; 1973 Jun 26; 25(1):54-70. PubMed ID: 4727733
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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
    [No Abstract] [Full Text] [Related]

  • 19. Histologic measurements and fine structure of biopsied sural nerve: normal, and in peroneal muscular atrophy, hypertrophic neuropathy, and congenital sensory neuropathy.
    Dyck PJ.
    Mayo Clin Proc; 1966 Nov 28; 41(11):742-74. PubMed ID: 4289252
    [No Abstract] [Full Text] [Related]

  • 20. [Roussy-Levy hereditary areflexic dysstasia. Its historical relation to Friedreich's disease, Charcot-Marie-Tooth atrophy and Dejerine-Sottas hypertrophic neuritis; the present status of the original family; the nosologic role of this entity].
    Lapresle J.
    Rev Neurol (Paris); 1982 Nov 28; 138(12):967-78. PubMed ID: 6763298
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.