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 *

173 related articles for article (PubMed ID: 15719054)

  • 1. [Molecular genetics of Charcot-Marie-Tooth disease].
    Zhang YZ; Zhong N
    Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):100-5. PubMed ID: 15719054
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.
    Niemann A; Berger P; Suter U
    Neuromolecular Med; 2006; 8(1-2):217-42. PubMed ID: 16775378
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease.
    Young P; Suter U
    Brain Res Brain Res Rev; 2001 Oct; 36(2-3):213-21. PubMed ID: 11690618
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.
    Houlden H; Reilly MM
    Neuromolecular Med; 2006; 8(1-2):43-62. PubMed ID: 16775366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Charcot-Marie-Tooth disease in Cyprus: epidemiological, clinical and genetic characteristics.
    Nicolaou P; Zamba-Papanicolaou E; Koutsou P; Kleopa KA; Georghiou A; Hadjigeorgiou G; Papadimitriou A; Kyriakides T; Christodoulou K
    Neuroepidemiology; 2010; 35(3):171-7. PubMed ID: 20571287
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.
    Verny C; Ravisé N; Leutenegger AL; Pouplard F; Dubourg O; Tardieu S; Dubas F; Brice A; Genin E; LeGuern E
    Neurology; 2004 Oct; 63(8):1527-9. PubMed ID: 15505184
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. How to assess the pathogenicity of mutations in Charcot-Marie-Tooth disease and other diseases?
    Kochański A
    J Appl Genet; 2006; 47(3):255-60. PubMed ID: 16877806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Charcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic heterogeneity.
    Lupski JR
    Pediatr Res; 1999 Feb; 45(2):159-65. PubMed ID: 10022584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.
    Azzedine H; Bolino A; Taïeb T; Birouk N; Di Duca M; Bouhouche A; Benamou S; Mrabet A; Hammadouche T; Chkili T; Gouider R; Ravazzolo R; Brice A; Laporte J; LeGuern E
    Am J Hum Genet; 2003 May; 72(5):1141-53. PubMed ID: 12687498
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Charcot-Marie-Tooth disease: an update.
    Shy ME
    Curr Opin Neurol; 2004 Oct; 17(5):579-85. PubMed ID: 15367862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T
    Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Autosomal recessive forms of Charcot-Marie-Tooth disease].
    Vallat JM; Grid D; Magdelaine C; Sturtz F; Levy N; Tazir M
    Bull Acad Natl Med; 2005 Jan; 189(1):55-68; discussion 68-9. PubMed ID: 16119880
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Charcot-Marie-Tooth disorders: past, today and tomorrow].
    Kochański A
    Neurol Neurochir Pol; 2006; 40(4):327-35. PubMed ID: 16967355
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic basis of inherited peripheral neuropathies.
    Suter U; Patel PI
    Hum Mutat; 1994; 3(2):95-102. PubMed ID: 7515304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1.
    Numakura C; Lin C; Oka N; Akiguchi I; Hayasaka K
    Ann Neurol; 2000 Jan; 47(1):101-3. PubMed ID: 10632107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dominantly inherited peripheral neuropathies.
    Vallat JM
    J Neuropathol Exp Neurol; 2003 Jul; 62(7):699-714. PubMed ID: 12901697
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo mutation of Charcot-Marie-Tooth disease type 1A.
    Tachi N; Kozuka N; Ohya K; Chiba S
    Pediatr Neurol; 1997 Jul; 17(1):67-9. PubMed ID: 9308980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The causes of Charcot-Marie-Tooth disease.
    Young P; Suter U
    Cell Mol Life Sci; 2003 Dec; 60(12):2547-60. PubMed ID: 14685682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.