These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

88 related articles for article (PubMed ID: 8618572)

  • 1. Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies.
    Kaneko S; Ito H; Kusaka H; Imai T; Nishimura T; Yoshikawa H
    Muscle Nerve; 1996 May; 19(5):675-6. PubMed ID: 8618572
    [No Abstract]   [Full Text] [Related]  

  • 2. [A family with hereditary neuropathy with liability to pressure palsies--clinical, electrophysiological, pathological study and DNA analysis].
    Kaneko S; Ito H; Kusaka H; Imai T; Yoshikawa H
    Rinsho Shinkeigaku; 1994 Jul; 34(7):673-8. PubMed ID: 7955724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.
    Nicholson GA; Valentijn LJ; Cherryson AK; Kennerson ML; Bragg TL; DeKroon RM; Ross DA; Pollard JD; McLeod JG; Bolhuis PA
    Nat Genet; 1994 Mar; 6(3):263-6. PubMed ID: 8012388
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 62(12):1911-4. PubMed ID: 16344349
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 14(12):804-9. PubMed ID: 15564036
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies.
    Mariman EC; Gabreëls-Festen AA; van Beersum SE; Valentijn LJ; Baas F; Bolhuis PA; Jongen PJ; Ropers HH; Gabreëls FJ
    Ann Neurol; 1994 Oct; 36(4):650-5. PubMed ID: 7944298
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 15(7):493-7. PubMed ID: 15955700
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A transgenic mouse model for human hereditary neuropathy with liability to pressure palsies.
    Maycox PR; Ortuño D; Burrola P; Kuhn R; Bieri PL; Arrezo JC; Lemke G
    Mol Cell Neurosci; 1997; 8(6):405-16. PubMed ID: 9143558
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 21(9):1199-201. PubMed ID: 9703447
    [TBL] [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; 44(4):290-4. PubMed ID: 17183456
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 263(1-2):194-7. PubMed ID: 17707409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ALS in a patient with hereditary neuropathy with liability to pressure palsy.
    O'Sullivan SS; McCarthy A; Mullins GM; McNamara B; Sweeney BJ
    Neurology; 2006 Dec; 67(12):2260. PubMed ID: 17190961
    [No Abstract]   [Full Text] [Related]  

  • 13. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
    Li J; Ghandour K; Radovanovic D; Shy RR; Krajewski KM; Shy ME; Nicholson GA
    Arch Neurol; 2007 Jul; 64(7):974-8. PubMed ID: 17620487
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary neuropathy with liability to pressure palsies: distinguishing clinical and electrophysiological features among patients with multiple entrapment neuropathy.
    Hirota N; Kaji R; Yoshikawa H; Nishimura T; Ikeda T; Yanagihara T; Kimura J
    J Neurol Sci; 1996 Aug; 139(2):187-9. PubMed ID: 8856651
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.
    Pareyson D; Solari A; Taroni F; Botti S; Fallica E; Scaioli V; Ciano C; Sghirlanzoni A
    Muscle Nerve; 1998 Dec; 21(12):1686-91. PubMed ID: 9843070
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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; 2000 Sep 16-30; 31(6):506-10. PubMed ID: 11055050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I; Arteaga R; García A; Herranz JL
    Rev Neurol; 2000 Jul 1-15; 31(1):38-41. PubMed ID: 10948581
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.
    Silander K; Meretoja P; Juvonen V; Ignatius J; Pihko H; Saarinen A; Wallden T; Herrgård E; Aula P; Savontaus ML
    Hum Mutat; 1998; 12(1):59-68. PubMed ID: 9633821
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.