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Journal Abstract Search

156 related items for PubMed ID: 12849887

  • 1. Hereditary neuropathy with liability to pressure palsies in infancy.
    Goikhman I, Meer J, Zelnik N.
    Pediatr Neurol; 2003 Apr; 28(4):307-9. PubMed ID: 12849887
    [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; 2003 Apr; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 3. Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene.
    van de Wetering RA, Gabreëls-Festen AA, Timmerman V, Padberg GM, Gabreëls FJ, Mariman EC.
    Neuromuscul Disord; 2002 Oct; 12(7-8):651-5. PubMed ID: 12207933
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary neuropathy with liability to pressure palsies in childhood: Report of three cases].
    Bar C, Villéga F, Espil C, Husson M, Pedespan JM, Rouanet MF.
    Arch Pediatr; 2017 Mar; 24(3):260-262. PubMed ID: 28131554
    [Abstract] [Full Text] [Related]

  • 5. Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion.
    Kim SM, Chung KW, Choi BO, Yoon ES, Choi JY, Park KD, Sunwoo IN.
    Exp Mol Med; 2004 Feb 29; 36(1):28-35. PubMed ID: 15031668
    [Abstract] [Full Text] [Related]

  • 6. [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 29; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [Abstract] [Full Text] [Related]

  • 7. A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.
    Muglia M, Patitucci A, Rizzi R, Ungaro C, Conforti FL, Gabriele AL, Magariello A, Mazzei R, Motti L, Sabadini R, Sprovieri T, Marcello N, Quattrone A.
    J Neurol Sci; 2007 Dec 15; 263(1-2):194-7. PubMed ID: 17707409
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 26(4):670-4. PubMed ID: 11466642
    [Abstract] [Full Text] [Related]

  • 9. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
    Chance PF.
    Neuromolecular Med; 2006 Jul 15; 8(1-2):159-74. PubMed ID: 16775374
    [Abstract] [Full Text] [Related]

  • 10. Hereditary neuropathy with liability to pressure palsy.
    Paprocka J, Kajor M, Jamroz E, Jezela-Stanek A, Seeman P, Marszał E.
    Folia Neuropathol; 2006 Jul 15; 44(4):290-4. PubMed ID: 17183456
    [Abstract] [Full Text] [Related]

  • 11. [Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought].
    Meretoja P, Silander K, Savontaus ML, Kalimo H.
    Duodecim; 1998 Jul 15; 114(24):2569-74. PubMed ID: 11757129
    [No Abstract] [Full Text] [Related]

  • 12. A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.
    Meuleman J, Pou-Serradell A, Löfgren A, Ceuterick C, Martin JJ, Timmerman V, Van Broeckhoven C, De Jonghe P.
    Neuromuscul Disord; 2001 May 15; 11(4):400-3. PubMed ID: 11369192
    [Abstract] [Full Text] [Related]

  • 13. Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies.
    Sutton IJ, Mocroft AP, Lindley VH, Barber RM, Bryon RJ, Winer JB, MacDonald F.
    Neuromuscul Disord; 2004 Dec 15; 14(12):804-9. PubMed ID: 15564036
    [Abstract] [Full Text] [Related]

  • 14. Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene.
    Stögbauer F, Young P, Kerschensteiner M, Ringelstein EB, Assmann G, Funke H.
    Muscle Nerve; 1998 Sep 15; 21(9):1199-201. PubMed ID: 9703447
    [Abstract] [Full Text] [Related]

  • 15. Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion.
    Gouider R, LeGuern E, Gugenheim M, Tardieu S, Maisonobe T, Léger JM, Vallat JM, Agid Y, Bouche P, Brice A.
    Neurology; 1995 Nov 15; 45(11):2018-23. PubMed ID: 7501152
    [Abstract] [Full Text] [Related]

  • 16. [Hereditary neuropathy with liability to pressure palsies caused by 17p11.2 chromosome deletion].
    Dorobek M, Szmidt-Sałkowska E, Drac H, Hardin A, Kwieciński H.
    Neurol Neurochir Pol; 1999 Nov 15; 33(1):177-85. PubMed ID: 10399735
    [Abstract] [Full Text] [Related]

  • 17. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I, Arteaga R, García A, Herranz JL.
    Rev Neurol; 1999 Nov 15; 31(1):38-41. PubMed ID: 10948581
    [Abstract] [Full Text] [Related]

  • 18. [Recurrent facial nerve paralysis in hereditary neuropathy with liability to pressure palsy].
    Drouet A, Guilloton L, Latour P, Ribot C.
    Presse Med; 2000 Apr 01; 29(12):655. PubMed ID: 10780201
    [No Abstract] [Full Text] [Related]

  • 19. Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy.
    Topakian R, Wimmer S, Pischinger B, Pichler R.
    BMJ Case Rep; 2014 Oct 17; 2014():. PubMed ID: 25326571
    [Abstract] [Full Text] [Related]

  • 20. Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.
    Yurrebaso I, Casado OL, Barcena J, Perez de Nanclares G, Aguirre U.
    Neuromuscul Disord; 2014 Jan 17; 24(1):56-62. PubMed ID: 24239057
    [Abstract] [Full Text] [Related]

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