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Journal Abstract Search

72 related items for PubMed ID: 8360575

  • 1. [A case of Dejerine-Sottas disease with central nervous system involvement].
    Katsuragi T, Hasegawa O, Takahashi T, Kubota H, Kawauchi Y.
    Nihon Naika Gakkai Zasshi; 1993 Jun 10; 82(6):914-5. PubMed ID: 8360575
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  • 2. The role of auditory brainstem response in diagnosing auditory impairments of Dejerine-Sottas.
    Talebi H, Rezazadeh N.
    Int J Pediatr Otorhinolaryngol; 2012 Jun 10; 76(6):915-7. PubMed ID: 22445798
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  • 3. MR imaging of Dejerine-Sottas disease.
    Maki DD, Yousem DM, Corcoran C, Galetta SL.
    AJNR Am J Neuroradiol; 1999 Mar 10; 20(3):378-80. PubMed ID: 10219400
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  • 4. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
    Sanahuja J, Franco E, Rojas-García R, Gallardo E, Combarros O, Begué R, Granés P, Illa I.
    Arch Neurol; 2005 Dec 10; 62(12):1911-4. PubMed ID: 16344349
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  • 5. CNS involvement in hereditary neuropathy with pressure palsies (HNPP).
    Tackenberg B, Möller JC, Rindock H, Bien S, Sommer N, Oertel WH, Rosenow F, Schepelmann K, Hamer HM, Bandmann O.
    Neurology; 2006 Dec 26; 67(12):2250-2. PubMed ID: 17190957
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  • 8. Hereditary motor sensory neuropathy (type 1) presenting with transient and persistent central nervous system manifestations: a novel genetic mutation.
    Absoud M, Brueton L, Gupta R, Quinlivan R, Wassmer E.
    Dev Med Child Neurol; 2011 Apr 26; 53(4):381-2. PubMed ID: 21309765
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  • 10. Juvenile-onset of Dejerine-Sottas disease in a Taiwanese woman.
    Liao YS, Chen ST, Tang LM, Ro LS.
    J Formos Med Assoc; 1996 Apr 26; 95(4):329-32. PubMed ID: 8935304
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  • 11. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul 26; 13(7):586-92. PubMed ID: 2388657
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  • 17. Study of brain stem auditory-evoked potentials (BAEPs) and visual-evoked potentials (VEPs) in leprosy.
    Kochar DK, Gupta DV, Sandeep C, Halwai M, Kumawat BL.
    Int J Lepr Other Mycobact Dis; 1997 Jun 26; 65(2):157-65. PubMed ID: 9251586
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  • 18. 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 26; 5(3):266-8. PubMed ID: 7506095
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  • 20. Jules Sottas (1866-1945) forgotten despite the eponym: "Dejerine-Sottas syndrome".
    Walusinski O.
    Rev Neurol (Paris); 2019 May 26; 175(5):283-290. PubMed ID: 30922590
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