155 related articles for article (PubMed ID: 4727733)
21. The importance of quantitative electron microscopy in studying hypertrophic neuropathies. A comparison between a case of Déjérine Sottas disease (HMSN III) and a case of the hypertrophic form of Charcot-Marie-Tooth disease (HMSN I).
Tredici G; Petruccioli-Pizzini MG; Gergely A; Coletti A
Int J Tissue React; 1984; 6(3):267-74. PubMed ID: 6090332
[TBL] [Abstract][Full Text] [Related]
22. [Ischialgia--peroneal muscular atrophy. Points about the disease picture of Tooth's type of progressive muscular atrophy and Déjerine-Sottas syndrome (author's transl)].
Ross A; Schrader A
Arch Orthop Unfallchir; 1974 Apr; 78(2):160-7. PubMed ID: 4275870
[No Abstract] [Full Text] [Related]
23. Hypertrophic neuropathy with spinal cord compression.
Carlin L; Biller J; Challa V; Riela A
Surg Neurol; 1982 Oct; 18(4):237-40. PubMed ID: 7179080
[TBL] [Abstract][Full Text] [Related]
24. 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; 41(11):742-74. PubMed ID: 4289252
[No Abstract] [Full Text] [Related]
25. [Muscular weakness, muscular atrophy, sensory disturbances, motor ataxia, articulation oculomotor and deglutition disorders and lingual atrophy: Dejerine-Sottas disease].
Goto F; Amano T
Nihon Rinsho; 1975 Apr; Spec No():932-3, 1418-21. PubMed ID: 1240429
[No Abstract] [Full Text] [Related]
26. A brief review of inherited hypertrophic neuropathy.
Dyck PJ
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):66-71. PubMed ID: 4950914
[No Abstract] [Full Text] [Related]
27. Hereditary hypertrophic neuropathy in the trembler mouse. Part 2. Histopathological studies: electron microscopy.
Low PA
J Neurol Sci; 1976 Dec; 30(2-3):343-68. PubMed ID: 187740
[TBL] [Abstract][Full Text] [Related]
28. 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; 31(1):15-7. PubMed ID: 4834537
[No Abstract] [Full Text] [Related]
29. [Familial fibula amyotrophies of neurogenic origin].
Vallat JM; Vital C
Cah Med; 1971 Jun; 12(10):803-15. PubMed ID: 4107838
[No Abstract] [Full Text] [Related]
30. [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; 138(12):967-78. PubMed ID: 6763298
[TBL] [Abstract][Full Text] [Related]
31. [X-ray computed tomography of lumbosacral roots and primary hypertrophic neuritis (Dejerine-Sottas disease)].
Mas JL; Buthiau D; Fallet-Bianco C; Cheron F; Raulo P; de Recondo J; Rondot P
Rev Neurol (Paris); 1989; 145(3):215-20. PubMed ID: 2749098
[TBL] [Abstract][Full Text] [Related]
32. Chronic neuropathy presenting as a floppy infant with respiratory distress.
Moss RB; Sriram S; Kelts KA; Forno LS; Lewiston NJ
Pediatrics; 1979 Oct; 64(4):459-64. PubMed ID: 492811
[TBL] [Abstract][Full Text] [Related]
33. [Pathogenic study of the Argyll-Robertson sign in Dejerine-Sottas hypertrophic neuritis. Anatomo-clinical record].
GARCIN R; GRUNER J; MAN HX
Presse Med (1893); 1960 Feb; 68():357-60. PubMed ID: 13826474
[No Abstract] [Full Text] [Related]
34. Experimental hypertrophic neuropathy. Pathogenesis of onion-bulb formations produced by repeated tourniquet applications.
Dyck PJ
Arch Neurol; 1969 Jul; 21(1):73-95. PubMed ID: 4890815
[No Abstract] [Full Text] [Related]
35. 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
[No Abstract] [Full Text] [Related]
36. Hereditary hypertrophic neuropathy in the trembler mouse. Part 1. Histopathological studies: light microscopy.
Low PA
J Neurol Sci; 1976 Dec; 30(2-3):327-41. PubMed ID: 187739
[TBL] [Abstract][Full Text] [Related]
37. Biopsy in a patient with PMP22 exon 2 mutation recapitulates pathology of Trembler-J mouse.
Madrid RE; Lofgren A; Baets J; Timmerman V
Neuromuscul Disord; 2013 Apr; 23(4):345-8. PubMed ID: 23313019
[TBL] [Abstract][Full Text] [Related]
38. 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
[TBL] [Abstract][Full Text] [Related]
39. Chronic relapsing polyradiculoneuritis in a cat.
Flecknell PA; Lucke VM
Acta Neuropathol; 1978 Jan; 41(1):81-4. PubMed ID: 636840
[TBL] [Abstract][Full Text] [Related]
40. The spinal cord-ventral root junction in the trembler mouse.
Harrison BM
Acta Neuropathol; 1977 Apr; 38(1):33-8. PubMed ID: 855650
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
