BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (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
    [TBL] [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; 2000 Sep 16-30; 31(6):506-10. PubMed ID: 11055050
    [TBL] [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
    [TBL] [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
    [TBL] [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; 36(1):28-35. PubMed ID: 15031668
    [TBL] [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; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [TBL] [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; 263(1-2):194-7. PubMed ID: 17707409
    [TBL] [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; 26(4):670-4. PubMed ID: 11466642
    [TBL] [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; 8(1-2):159-74. PubMed ID: 16775374
    [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. [Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought].
    Meretoja P; Silander K; Savontaus ML; Kalimo H
    Duodecim; 1998; 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; 11(4):400-3. PubMed ID: 11369192
    [TBL] [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; 14(12):804-9. PubMed ID: 15564036
    [TBL] [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; 21(9):1199-201. PubMed ID: 9703447
    [TBL] [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; 45(11):2018-23. PubMed ID: 7501152
    [TBL] [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; 33(1):177-85. PubMed ID: 10399735
    [TBL] [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; 2000 Jul 1-15; 31(1):38-41. PubMed ID: 10948581
    [TBL] [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; 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; 2014():. PubMed ID: 25326571
    [TBL] [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; 24(1):56-62. PubMed ID: 24239057
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.