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145 related items for PubMed ID: 35595399

  • 1. Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion.
    Pabón Meneses RM, Azcona Ganuza G, Urriza Mena J, Ibiricu Yanguas A, Gila Useros L, García de Gurtubay I.
    Neurologia (Engl Ed); 2022 May; 37(4):243-249. PubMed ID: 35595399
    [Abstract] [Full Text] [Related]

  • 2. Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion.
    Pabón Meneses RM, Azcona Ganuza G, Urriza Mena J, Ibiricu Yanguas A, Gila Useros L, García de Gurtubay I.
    Neurologia (Engl Ed); 2022 May; 37(4):243-249. PubMed ID: 31047731
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 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 28; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [Abstract] [Full Text] [Related]

  • 5. [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; 2002 May 28; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion.
    Hong YH, Kim M, Kim HJ, Sung JJ, Kim SH, Lee KW.
    Acta Neurol Scand; 2003 Nov 29; 108(5):352-8. PubMed ID: 14616306
    [Abstract] [Full Text] [Related]

  • 8. Pain and small-fiber affection in hereditary neuropathy with liability to pressure palsies (HNPP).
    Dukefoss TT, Kleggetveit IP, Helås T, Jørum E.
    Scand J Pain; 2019 Dec 18; 20(1):61-68. PubMed ID: 31536037
    [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 Dec 18; 8(1-2):159-74. PubMed ID: 16775374
    [Abstract] [Full Text] [Related]

  • 10. Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria.
    Robert-Varvat F, Jousserand G, Bouhour F, Vial C, Cintas P, Echaniz-Laguna A, Delmont E, Clavelou P, Chauplannaz G, Jomir L, Pereon Y, Leonard-Louis S, Manel V, Antoine JC, Lacour A, Camdessanche JP.
    Muscle Nerve; 2018 Feb 18; 57(2):217-221. PubMed ID: 28407266
    [Abstract] [Full Text] [Related]

  • 11. Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion.
    Mouton P, Tardieu S, Gouider R, Birouk N, Maisonobe T, Dubourg O, Brice A, LeGuern E, Bouche P.
    Neurology; 1999 Apr 22; 52(7):1440-6. PubMed ID: 10227632
    [Abstract] [Full Text] [Related]

  • 12. [Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure].
    Pou Serradell A, Espadaler JM, Aragonés JM, Bufill E, Alameda F, Vílchez JJ, Sevilla T, Piqueras A, Palau F, Bort S.
    Neurologia; 1995 Nov 22; 10(9):367-74. PubMed ID: 8554792
    [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 22; 24(1):56-62. PubMed ID: 24239057
    [Abstract] [Full Text] [Related]

  • 14. 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 22; 35(6):704-8. PubMed ID: 8210227
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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]

  • 17. 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]

  • 18. 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 15; 20(2):79-85. PubMed ID: 26110377
    [Abstract] [Full Text] [Related]

  • 19. Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population.
    Park JE, Noh SJ, Oh M, Cho DY, Kim SY, Ki CS.
    Orphanet J Rare Dis; 2018 Mar 15; 13(1):40. PubMed ID: 29544507
    [Abstract] [Full Text] [Related]

  • 20. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.
    Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R, Finelli P, Archidiacono N.
    Muscle Nerve; 1995 Jun 15; 18(6):628-35. PubMed ID: 7753126
    [Abstract] [Full Text] [Related]

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