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Journal Abstract Search

214 related items for PubMed ID: 24668782

  • 1. Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy.
    Potulska-Chromik A, Sinkiewicz-Darol E, Ryniewicz B, Lipowska M, Kabzińska D, Kochański A, Kostera-Pruszczyk A.
    Muscle Nerve; 2014 Dec; 50(6):914-8. PubMed ID: 24668782
    [Abstract] [Full Text] [Related]

  • 2. Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update.
    Chrestian N, McMillan H, Poulin C, Campbell C, Vajsar J.
    Neuromuscul Disord; 2015 Sep; 25(9):693-8. PubMed ID: 26189194
    [Abstract] [Full Text] [Related]

  • 3. Mutational analysis of Greek patients with suspected hereditary neuropathy with liability to pressure palsies (HNPP): a 15-year experience.
    Karadima G, Koutsis G, Raftopoulou M, Karletidi KM, Zambelis T, Karandreas N, Panas M.
    J Peripher Nerv Syst; 2015 Jun; 20(2):79-85. PubMed ID: 26110377
    [Abstract] [Full Text] [Related]

  • 4. Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP).
    Chen B, Niu S, Wang X, Li W, Chen N, Zhang Z.
    J Clin Neurosci; 2018 Feb; 48():133-137. PubMed ID: 29108667
    [Abstract] [Full Text] [Related]

  • 5. Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.
    Fusco C, Spagnoli C, Salerno GG, Pavlidis E, Frattini D, Pisani F.
    Ital J Pediatr; 2017 Oct 27; 43(1):97. PubMed ID: 29078790
    [Abstract] [Full Text] [Related]

  • 6. Hereditary neuropathy with liability to pressure palsy: a brief review with a case report.
    Rana AQ, Masroor MS.
    Int J Neurosci; 2012 Mar 27; 122(3):119-23. PubMed ID: 22023293
    [Abstract] [Full Text] [Related]

  • 7. [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 27; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [Abstract] [Full Text] [Related]

  • 8. [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 27; 32(1):31-5. PubMed ID: 25636095
    [Abstract] [Full Text] [Related]

  • 9. Early-onset hereditary neuropathy with liability to pressure palsy.
    Antonini G, Luchetti A, Mastrangelo M, Ciambra GL, Di Netta S, Taioli F, Fabrizi GM, Iannetti P.
    Neuropediatrics; 2007 Feb 27; 38(1):50-4. PubMed ID: 17607607
    [Abstract] [Full Text] [Related]

  • 10. Proximal arm weakness is the most common presentation in young Korean soldiers diagnosed as having hereditary neuropathy with liability to pressure palsy (HNPP).
    Kim KE, Yeom J.
    J R Army Med Corps; 2016 Oct 27; 162(5):352-354. PubMed ID: 26462743
    [Abstract] [Full Text] [Related]

  • 11. Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.
    Beydoun SR, Cho J.
    J Clin Neuromuscul Dis; 2013 Sep 27; 15(1):28-33. PubMed ID: 23965407
    [Abstract] [Full Text] [Related]

  • 12. 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 27; 24(1):56-62. PubMed ID: 24239057
    [Abstract] [Full Text] [Related]

  • 13. The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseases.
    Sinkiewicz-Darol E, Lacerda AF, Kostera-Pruszczyk A, Potulska-Chromik A, Sokołowska B, Kabzińska D, Brunetti CR, Hausmanowa-Petrusewicz I, Kochański A.
    Neurogenetics; 2015 Jan 27; 16(1):27-32. PubMed ID: 25342198
    [Abstract] [Full Text] [Related]

  • 14. Characteristic features of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy in soldiers.
    Kim KE.
    J Neurol Sci; 2014 Nov 15; 346(1-2):174-7. PubMed ID: 25175852
    [Abstract] [Full Text] [Related]

  • 15. A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.
    D'Arrigo S, Tessarollo V, Taroni F, Baratta S, Pantaleoni C, Schiaffi E, Ciano C.
    Neuropediatrics; 2020 Jun 15; 51(3):173-177. PubMed ID: 31784971
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. The phenotype of the Gly94fsX222 PMP22 insertion.
    de Vries SD, Verhamme C, van Ruissen F, van Paassen BW, Arts WF, Kerkhoff H, van Engelen BG, Lammens M, de Visser M, Baas F, van der Kooi AJ.
    J Peripher Nerv Syst; 2011 Jun 15; 16(2):113-8. PubMed ID: 21692910
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  • 19. A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: the value of complete electrodiagnostic testing.
    Bulusu S, McMillan HJ.
    Am J Electroneurodiagnostic Technol; 2011 Sep 15; 51(3):183-90. PubMed ID: 21988036
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