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 *

119 related articles for article (PubMed ID: 7855009)

  • 1. 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]  

  • 2. 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]  

  • 3. Nerve root and sciatic trunk enlargement in Déjérine-Sottas disease: MRI appearances.
    Masuda N; Hayashi H; Tanabe H
    Neuroradiology; 1992; 35(1):36-7. PubMed ID: 1289736
    [No Abstract]   [Full Text] [Related]  

  • 4. Dejerine-Sottas disease: a case report.
    Marinho JL; Alonso Nieto JL; Calore EE
    Sao Paulo Med J; 2003 Sep; 121(5):207-9. PubMed ID: 14666293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.
    Tachi N; Kozuka N; Ohya K; Chiba S; Naganuma M
    Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Dejerine-sottas disease with a novel de novo dominant mutation, Ser 149 Arg, of the peripheral myelin protein 22.
    Ohnishi A; Yamamoto T; Izawa K; Yamamori S; Takahashi K; Mega H; Jinnai K
    Acta Neuropathol; 2000 Mar; 99(3):327-30. PubMed ID: 10663978
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dejerine-Sottas' neuropathy caused by the missense mutation PMP22 Ser72Leu.
    Marques W; Neto JM; Barreira AA
    Acta Neurol Scand; 2004 Sep; 110(3):196-9. PubMed ID: 15285778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sensory-motor hereditary neuropathy with early onset. A case report.
    Malandrini A; De Stefano N; Dotti MT; Vecchione V; Federico A
    Acta Neurol (Napoli); 1993 Apr; 15(2):81-6. PubMed ID: 8328327
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
    Plante-Bordeneuve V; Said G
    Muscle Nerve; 2002 Nov; 26(5):608-21. PubMed ID: 12402282
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking.
    Patzig J; Kusch K; Fledrich R; Eichel MA; Lüders KA; Möbius W; Sereda MW; Nave KA; Martini R; Werner HB
    Glia; 2016 Jan; 64(1):155-74. PubMed ID: 26393339
    [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. Giant axonal neuropathy in two siblings: clinical histopathological findings.
    Hergüner MO; Zorludemir S; Altunbasak S
    Clin Neuropathol; 2005; 24(1):48-50. PubMed ID: 15696785
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases.
    Planté-Bordeneuve V; Parman Y; Guiochon-Mantel A; Alj Y; Deymeer F; Serdaroglu P; Eraksoy M; Said G
    J Neurol; 2001 Sep; 248(9):795-803. PubMed ID: 11596785
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0.
    Simonati A; Fabrizi GM; Taioli F; Polo A; Cerini R; Rizzuto N
    J Neurol; 2002 Sep; 249(9):1298-302. PubMed ID: 12242557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Giant axonal neuropathy in a child with insulin-dependent diabetes mellitus.
    Hoffman WH; Carroll JE; Perry GY; Hartlage PL; Kaminer SJ; Flowers NC; Oh SJ; Kelly DR
    J Child Neurol; 1995 May; 10(3):250-3. PubMed ID: 7642902
    [No Abstract]   [Full Text] [Related]  

  • 19. [Hereditary motor and sensory neuropathy type III. Case report and review of the literature].
    Haverkamp F; Behring B
    Klin Padiatr; 1995; 207(1):24-7. PubMed ID: 7885014
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom.
    King RH; Tournev I; Colomer J; Merlini L; Kalaydjieva L; Thomas PK
    Neuropathol Appl Neurobiol; 1999 Aug; 25(4):306-12. PubMed ID: 10476047
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.