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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]
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]
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]
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]