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Journal Abstract Search

240 related items for PubMed ID: 15804150

  • 1. 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; 28(1):56-63. PubMed ID: 15804150
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [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; 2004 Feb 29; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. Hereditary neuropathy with liability to pressure palsy.
    Paprocka J, Kajor M, Jamroz E, Jezela-Stanek A, Seeman P, Marszał E.
    Folia Neuropathol; 2006 May 29; 44(4):290-4. PubMed ID: 17183456
    [Abstract] [Full Text] [Related]

  • 6. 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 29; 35(6):704-8. PubMed ID: 8210227
    [Abstract] [Full Text] [Related]

  • 7. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
    Chance PF.
    Neuromolecular Med; 2006 Jun 29; 8(1-2):159-74. PubMed ID: 16775374
    [Abstract] [Full Text] [Related]

  • 8. 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 29; 11(4):400-3. PubMed ID: 11369192
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. [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]

  • 11. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I, Arteaga R, García A, Herranz JL.
    Rev Neurol; 1989 Apr 02; 31(1):38-41. PubMed ID: 10948581
    [Abstract] [Full Text] [Related]

  • 12. [Analysis of the clinical, electrophysiological and genetic features of a family affected with hereditary neuropathy with liability to pressure palsies].
    Qi F, Che F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb 02; 32(1):31-5. PubMed ID: 25636095
    [Abstract] [Full Text] [Related]

  • 13. 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 02; 24(1):56-62. PubMed ID: 24239057
    [Abstract] [Full Text] [Related]

  • 14. Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience.
    Luigetti M, Del Grande A, Conte A, Lo Monaco M, Bisogni G, Romano A, Zollino M, Rossini PM, Sabatelli M.
    J Neurol Sci; 2014 Jun 15; 341(1-2):46-50. PubMed ID: 24726093
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Clinical and electrodiagnostic findings, nerve biopsy and blood group markers in a family with hereditary neuropathy with liability to pressure palsies.
    Leblhuber F, Reisecker F, Willeit J, Windhager E, Witzmann A, Mayr WR.
    Acta Neurol Scand; 1991 Mar 15; 83(3):166-71. PubMed ID: 1827702
    [Abstract] [Full Text] [Related]

  • 17. Hereditary neuropathy with liability to pressure palsies: assocation with central nervous system demyelination.
    Amato AA, Barohn RJ.
    Muscle Nerve; 1996 Jun 15; 19(6):770-3. PubMed ID: 8609929
    [Abstract] [Full Text] [Related]

  • 18. Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.
    Cao W, Huang S, Zhao H, Li Z, Zhu X, Liu L, Zhang R.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Oct 28; 48(10):1572-1582. PubMed ID: 38432886
    [Abstract] [Full Text] [Related]

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