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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 12984160)

  • 1. [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]  

  • 2. [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]  

  • 3. Progressive familial hypertrophic polyneuritis (Dejerine-Sottas Syndrome, 1893).
    COX MJ
    Proc R Soc Med; 1956 Apr; 49(4):183-4. PubMed ID: 13322918
    [No Abstract]   [Full Text] [Related]  

  • 4. [Clinical, histologic and genealogic aspects of Déjerine-Sottas disease].
    CREUTZFELDT HG; CURTIUS F; KRUGER KH
    Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr; 1951; 186(4):341-60. PubMed ID: 14857718
    [No Abstract]   [Full Text] [Related]  

  • 5. Jules Sottas (1866-1945) forgotten despite the eponym: "Dejerine-Sottas syndrome".
    Walusinski O
    Rev Neurol (Paris); 2019 May; 175(5):283-290. PubMed ID: 30922590
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Phrenic nerve involvement in Déjérine-Sottas disease: a clinicopathological case study.
    Felice KJ; Fratkin JD; Feldman EL; Sima AA
    Pediatr Pathol; 1994; 14(6):905-11. PubMed ID: 7855009
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ; Kuntz NL; Miller RG; Daube JR
    Muscle Nerve; 1990 Jul; 13(7):586-92. PubMed ID: 2388657
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. MR imaging of Dejerine-Sottas disease.
    Maki DD; Yousem DM; Corcoran C; Galetta SL
    AJNR Am J Neuroradiol; 1999 Mar; 20(3):378-80. PubMed ID: 10219400
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
    Ikegami T; Nicholson G; Ikeda H; Ishida A; Johnston H; Wise G; Ouvrier R; Hayasaka K
    Biochem Biophys Res Commun; 1996 May; 222(1):107-10. PubMed ID: 8630052
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Dejerine-Sottas disease (progressive hypertrophic polyneuropathy).
    Pearce JM
    Eur Neurol; 2006; 55(2):115-7. PubMed ID: 16645280
    [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; 25(1):54-70. PubMed ID: 4727733
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. 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]  

  • 20. [Records useful for the pathogenic study of the Argyll-Robertson sign in Dejerine-Sottas hypertrophic interstitial neuritis].
    GARCIN R; GRUNER J; MAN HX
    Bull Acad Natl Med; 1959 Jun 7-Jul 23; 143():499-508. PubMed ID: 13826475
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.