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.
2. A family with the progressive hypertrophic polyneuritis of Dejerine and Sottas. BEDFORD PD; JAMES FE J Neurol Neurosurg Psychiatry; 1956 Feb; 19(1):46-51. PubMed ID: 13320157 [No Abstract] [Full Text] [Related]
3. [Dejerine-Sottas hypertrophic interstitial neuritis and von Recklinghausen's neurofibromatosis]. ORTIZ de ZARATE JC; RUGGIERI F Prensa Med Argent; 1950 Sep; 37(37):2181-91. PubMed ID: 14781018 [No Abstract] [Full Text] [Related]
4. [Case of Dejerine-Sottas type of interstitial-hypertrophic neuritis limited to the median nerve]. MEDEA E Sist Nerv; 1950; 2(2):131-3. PubMed ID: 12984160 [No Abstract] [Full Text] [Related]
9. A case of progressive hypertrophic neuropathy in childhood with facial diplegia (Dejerine-Sottas disease). Sunwoo IN; Kim JS; Chi JG; Suh YL Yonsei Med J; 1988; 29(3):278-85. PubMed ID: 3195160 [No Abstract] [Full Text] [Related]
10. [Two cases of sporadic hypertrophic progressive neuritis of Dejerine-Sottas type with biopsy control]. GARCIN R; BERTRAND I; FREITAS-JULIAO O; BUGE Rev Neurol (Paris); 1950 Mar; 82(3):204-10. PubMed ID: 15441713 [No Abstract] [Full Text] [Related]
11. Observations on hypertrophic neuropathy of Dejerine and Sottas. ANDERMANN F; LLOYD-SMITH DL; MAVOR H; MATHIESON G Neurology; 1962 Oct; 12():712-24. PubMed ID: 13861139 [No Abstract] [Full Text] [Related]
12. 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]
13. Hypertrophic peripheral neuropathy (Dejerine-Sottas disease) associated with heart block. Case report presentation and review of the literature. Kouvaras G; Chronopoulos G; Pistis G; Cokkinos D Jpn Heart J; 1990 May; 31(3):405-10. PubMed ID: 2214139 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. Lipid abnormalities in hereditary neuropathy. Part 3. Plasma and erythrocyte lipids of HMSN-III (Dejerine-Sottas disease). Yao JK; Dyck PJ J Neurol Sci; 1978 Aug; 38(1):59-65. PubMed ID: 702184 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. Juvenile-onset of Dejerine-Sottas disease in a Taiwanese woman. Liao YS; Chen ST; Tang LM; Ro LS J Formos Med Assoc; 1996 Apr; 95(4):329-32. PubMed ID: 8935304 [TBL] [Abstract][Full Text] [Related]
18. [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]
19. [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]
20. De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Hayasaka K; Himoro M; Sawaishi Y; Nanao K; Takahashi T; Takada G; Nicholson GA; Ouvrier RA; Tachi N Nat Genet; 1993 Nov; 5(3):266-8. PubMed ID: 7506095 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]