BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

332 related articles for article (PubMed ID: 11098291)

  • 1. Molecular genetics of inherited peripheral neuropathies: who are the actors?
    Meuleman J; Timmerman V; Nelis E; De Jonghe P
    Acta Neurol Belg; 2000 Sep; 100(3):171-80. PubMed ID: 11098291
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.
    Nelis E; Haites N; Van Broeckhoven C
    Hum Mutat; 1999; 13(1):11-28. PubMed ID: 9888385
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Common themes in peripheral neuropathy disease genes.
    Snipes GJ; Orfali W
    Cell Biol Int; 1998 Nov; 22(11-12):815-35. PubMed ID: 10873294
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.
    Huehne K; Benes V; Thiel C; Kraus C; Kress W; Hoeltzenbein M; Ploner CJ; Kotzian J; Reis A; Rott HD; Rautenstrauss BW
    Hum Mutat; 2003 Jan; 21(1):100. PubMed ID: 12497641
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Charcot-Marie-Tooth disease and related peripheral neuropathies.
    De Jonghe P; Timmerman V; Nelis E; Martin JJ; Van Broeckhoven C
    J Peripher Nerv Syst; 1997; 2(4):370-87. PubMed ID: 10975746
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.
    Mostacciuolo ML; Righetti E; Zortea M; Bosello V; Schiavon F; Vallo L; Merlini L; Siciliano G; Fabrizi GM; Rizzuto N; Milani M; Baratta S; Taroni F
    Hum Mutat; 2001; 18(1):32-41. PubMed ID: 11438991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mutation testing in Charcot-Marie-Tooth neuropathy.
    Nicholson GA
    Ann N Y Acad Sci; 1999 Sep; 883():383-8. PubMed ID: 10586262
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peripheral myelin protein 22 kDa and protein zero: domain specific trans-interactions.
    Hasse B; Bosse F; Hanenberg H; Müller HW
    Mol Cell Neurosci; 2004 Dec; 27(4):370-8. PubMed ID: 15555916
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].
    Hayasaka K
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1444-6. PubMed ID: 8752425
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.
    Mersiyanova IV; Ismailov SM; Polyakov AV; Dadali EL; Fedotov VP; Nelis E; Löfgren A; Timmerman V; van Broeckhoven C; Evgrafov OV
    Hum Mutat; 2000; 15(4):340-7. PubMed ID: 10737979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32), peripheral myelin protein 22 (PMP22), and peripheral myelin protein zero (MPZ).
    Ekici AB; Schweitzer D; Park O; Lorek D; Rautenstrauss B; Krüger G; Friedl W; Uhlhaas S; Bathke K; Heuss D; Kayser C; Grehl H
    Neurogenetics; 2000 Sep; 3(1):49-50. PubMed ID: 11085599
    [No Abstract]   [Full Text] [Related]  

  • 14. [Advances in the molecular genetics of the hereditary neuropathies].
    Palau F; Cuesta A; Pedrola L
    Rev Neurol; 2002 Aug 1-15; 35(3):246-53. PubMed ID: 12235587
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Electrophysiologic features of inherited demyelinating neuropathies: a reappraisal.
    Lewis RA; Sumner AJ
    Ann N Y Acad Sci; 1999 Sep; 883():321-35. PubMed ID: 10586257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C; Baas F
    Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Charcot-Marie-Tooth disease: frequency of genetic subtypes in a German neuromuscular center population.
    Gess B; Schirmacher A; Boentert M; Young P
    Neuromuscul Disord; 2013 Aug; 23(8):647-51. PubMed ID: 23743332
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of Charcot-Marie-Tooth disease.
    Pleasure DE
    Arch Neurol; 2003 Apr; 60(4):481-2. PubMed ID: 12707058
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutations in demyelinating peripheral neuropathies support molecular model of myelin P0-glycoprotein extracellular domain.
    Kirschner DA; Saavedra RA
    J Neurosci Res; 1994 Sep; 39(1):63-9. PubMed ID: 7528817
    [TBL] [Abstract][Full Text] [Related]  

  • 20. P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.
    Martini R
    Ann N Y Acad Sci; 1999 Sep; 883():273-80. PubMed ID: 10586252
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.