89 related articles for article (PubMed ID: 4300473)
1. Hypertrophic neuropathy: a report of Dejerine-Sottas disease in two sibs.
O'Brien MD
Guys Hosp Rep; 1968; 117(2):79-88. PubMed ID: 4300473
[No Abstract] [Full Text] [Related]
2. Histologic and lipid studies of sural nerves in inherited hypertrophic neuropathy: preliminary report of a lipid abnormality in nerve and liver in Dejerine-Sottas disease.
Dyck PJ; Ellefson RD; Lais AC; Smith RC; Taylor WF; Van Dyke RA
Mayo Clin Proc; 1970 Apr; 45(4):286-327. PubMed ID: 4314714
[No Abstract] [Full Text] [Related]
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; 1975 Jul 10-20; 51(31-34):2103-7. PubMed ID: 52195
[TBL] [Abstract][Full Text] [Related]
4. Hypertrophic neuropathy.
Lancet; 1967 Jun; 1(7501):1202-3. PubMed ID: 4165139
[No Abstract] [Full Text] [Related]
5. Hereditary polyneuropathy of Roussy-Lévy type with associated cardiomyopathy.
Lascelles RG; Baker IA; Thomas PK
Guys Hosp Rep; 1970; 119(3):253-62. PubMed ID: 4321562
[No Abstract] [Full Text] [Related]
6. Dejerine-Sottas disease revisited.
Satran R
Arch Neurol; 1980 Feb; 37(2):67-8. PubMed ID: 7356409
[TBL] [Abstract][Full Text] [Related]
7. [Degenerative myelo-radiculo-neuropathy. Review of the literature concerning Dejerine-Sottas disease, Charcot-Marie-Tooth disease and the Roussy-Lévy syndrome. Presentation of 6 personal cases].
Spinnler H
Sist Nerv; 1968; 20(3):147-237. PubMed ID: 4314017
[No Abstract] [Full Text] [Related]
8. [Genetic considerations on a series of cases of peripheral neuropathy of the hereditary paramyloidosis type].
Fariello R; Curtoni ES; Delsedime M; Mutani R; Quattrocolo G; Fariello R; Furlan PM
Arch Sci Med (Torino); 1971; 128(4):181-5. PubMed ID: 4342668
[No Abstract] [Full Text] [Related]
9. [Clinical study of muscular atrophy].
Shinoda M
Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121
[No Abstract] [Full Text] [Related]
10. 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]
11. [Tumor-like transformation of the median nerve in neural muscular atrophy].
Goth D; Ketelsen UP
Handchir Mikrochir Plast Chir; 1983 Dec; 15(4):238-40. PubMed ID: 6317529
[TBL] [Abstract][Full Text] [Related]
12. Idiopathic shoulder girdle neuropathy.
Weaver K; Kraft GH
Phys Med Rehabil Clin N Am; 2001 May; 12(2):353-64, x. PubMed ID: 11345012
[TBL] [Abstract][Full Text] [Related]
13. [Delerium patterns in Déjerine-Sottas disease].
Barcia D; Muñóz R
Actas Luso Esp Neurol Psiquiatr Cienc Afines; 1980; 8(5):337-46. PubMed ID: 7457222
[No Abstract] [Full Text] [Related]
14. Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type.
Gutmann L; Fakadej A; Riggs JE
Muscle Nerve; 1983 Sep; 6(7):515-9. PubMed ID: 6314135
[TBL] [Abstract][Full Text] [Related]
15. [Case of Déjerine-Sottas disease with schizophrenic symptoms].
Nakao T; Okuma T; Matsushima Y; Takahashi K; Nagami M
Rinsho Shinkeigaku; 1972 Mar; 12(3):149-57. PubMed ID: 4674763
[No Abstract] [Full Text] [Related]
16. [A case of localized hypertrophic neuropathy in the sciatic nerve].
Izumi T; Kusaka H; Imai T
Rinsho Shinkeigaku; 1995 Jan; 35(1):38-43. PubMed ID: 7781213
[TBL] [Abstract][Full Text] [Related]
17. Hereditary hypertrophic neuropathy. Report of two cases of an autosomal recessive variant.
Kalyanaraman K; Cancilla PA; Munsat T; Pearson CM
Bull Los Angeles Neurol Soc; 1970 Apr; 35(2):58-68. PubMed ID: 4314732
[No Abstract] [Full Text] [Related]
18. Hypertrophic interstitial neuropathy of Déjérine-Sottas.
Beighton PH
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):103-4. PubMed ID: 5173113
[No Abstract] [Full Text] [Related]
19. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene.
Roa BB; Dyck PJ; Marks HG; Chance PF; Lupski JR
Nat Genet; 1993 Nov; 5(3):269-73. PubMed ID: 8275092
[TBL] [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; 138(12):967-78. PubMed ID: 6763298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
