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PUBMED FOR HANDHELDS

Journal Abstract Search


115 related items for PubMed ID: 2290479

  • 1. Steroid responsive familial neuropathy with liability to pressure palsies.
    Barisić N, Skarpa D, Jusić A, Jadro-Santel D.
    Neuropediatrics; 1990 Nov; 21(4):191-2. PubMed ID: 2290479
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
    Eirís-Punal J, Vidal-Lijó M, Barros-Angueira F, Lopez-Fernández MJ, Pintos-Martínez E, Beiras-Iglesias A, Castro-Gago M.
    Rev Neurol; 1990 Nov; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary neuropathy with liability to pressure palsy].
    Eisenberg E, Baron S, Ludicer R.
    Harefuah; 1989 Apr 02; 116(7):345-7. PubMed ID: 2737556
    [Abstract] [Full Text] [Related]

  • 4. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.
    Verhalle D, Löfgren A, Nelis E, Dehaene I, Theys P, Lammens M, Dom R, Van Broeckhoven C, Robberecht W.
    Ann Neurol; 1994 Jun 02; 35(6):704-8. PubMed ID: 8210227
    [Abstract] [Full Text] [Related]

  • 5. Tomaculous neuropathy: hereditary predisposition to pressure palsies.
    Fewings JD, Blumbergs PC, Mukherjee TM, Hallpike JF.
    Aust N Z J Med; 1985 Oct 02; 15(5):598-603. PubMed ID: 3004403
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought].
    Meretoja P, Silander K, Savontaus ML, Kalimo H.
    Duodecim; 1998 Oct 02; 114(24):2569-74. PubMed ID: 11757129
    [No Abstract] [Full Text] [Related]

  • 7. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug 02; 35(8):843-9. PubMed ID: 8665724
    [Abstract] [Full Text] [Related]

  • 8. Hereditary neuropathy with liability to pressure palsies: a clinical and genetic study of a Taiwanese family.
    Tsai YT, Kuo HC, Chu CC, Lin KP, Huang CC.
    Chang Gung Med J; 2005 Jan 02; 28(1):56-63. PubMed ID: 15804150
    [Abstract] [Full Text] [Related]

  • 9. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I, Arteaga R, García A, Herranz JL.
    Rev Neurol; 2005 Jan 02; 31(1):38-41. PubMed ID: 10948581
    [Abstract] [Full Text] [Related]

  • 10. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
    Pou Serradell A, Monells J, Téllez MJ, Fossas P, Löfgren A, Meuleman J, Timmerman V, De Jonghe P, Ceuterick C, Martin JJ.
    Rev Neurol (Paris); 2002 May 02; 158(5 Pt 1):579-88. PubMed ID: 12072826
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  • 15. Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation.
    Del Colle R, Fabrizi GM, Turazzini M, Cavallaro T, Silvestri M, Rizzuto N.
    Neurol Sci; 2003 Jun 02; 24(2):57-60. PubMed ID: 12827539
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  • 16. Hereditary neuropathy with liability to pressure palsies mimicking multifocal compression neuropathy.
    Lane JE, Foulkes GD, Hope TD, Mayorov VI, Adkison L.
    J Hand Surg Am; 2001 Jul 02; 26(4):670-4. PubMed ID: 11466642
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  • 17. [Hereditary neuropathy with liability to pressure palsies].
    Smith TA, Rasmussen K, Hertz JM.
    Ugeskr Laeger; 1999 Jun 07; 161(23):3463-5. PubMed ID: 10388355
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  • 18. Nerve and muscle biopsy in a case of hereditary motor and sensory neuropathy type III with basal lamina onion bulbs.
    Bornemann A, Hansen FJ, Schmalbruch H.
    Neuropathol Appl Neurobiol; 1996 Feb 07; 22(1):77-81. PubMed ID: 8866786
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  • 19. 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 07; 62(12):1911-4. PubMed ID: 16344349
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  • 20. A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies.
    Zéphir H, Stojkovic T, Latour P, Hurtevent JF, Blankaert F, Vermersch P.
    Neuromuscul Disord; 2005 Jul 07; 15(7):493-7. PubMed ID: 15955700
    [Abstract] [Full Text] [Related]


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