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 *

91 related articles for article (PubMed ID: 15602373)

  • 1. [Charcot-Marie-Tooth disease: from phenotype to genotype].
    Dubourg O
    Rev Neurol (Paris); 2004 Dec; 160(12):1221-9. PubMed ID: 15602373
    [No Abstract]   [Full Text] [Related]  

  • 2. Charcot-Marie-Tooth disease.
    Szigeti K; Lupski JR
    Eur J Hum Genet; 2009 Jun; 17(6):703-10. PubMed ID: 19277060
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Axonal Charcot-Marie-Tooth disease: the fog is only slowly lifting.
    Pareyson D
    Neurology; 2007 May; 68(20):1649-50. PubMed ID: 17502544
    [No Abstract]   [Full Text] [Related]  

  • 4. Axonal Charcot-Marie-Tooth disease: the fog is slowly lifting!
    Reilly MM
    Neurology; 2005 Jul; 65(2):186-7. PubMed ID: 16043782
    [No Abstract]   [Full Text] [Related]  

  • 5. Pediatric Charcot-Marie-Tooth disease.
    Jani-Acsadi A; Ounpuu S; Pierz K; Acsadi G
    Pediatr Clin North Am; 2015 Jun; 62(3):767-86. PubMed ID: 26022174
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Some considerations on atypical cases of Charcot-Marie-Tooth disease and use of genetic testing in idiopathic polyneuropathies.
    Mondelli M; Fabrizi GM
    Clin Neurol Neurosurg; 2010 Nov; 112(9):745-6. PubMed ID: 20800965
    [No Abstract]   [Full Text] [Related]  

  • 7. Phenotype of Charcot-Marie-Tooth disease Type 2.
    Bienfait HM; Baas F; Koelman JH; de Haan RJ; van Engelen BG; Gabreëls-Festen AA; Ongerboer de Visser BW; Meggouh F; Weterman MA; De Jonghe P; Timmerman V; de Visser M
    Neurology; 2007 May; 68(20):1658-67. PubMed ID: 17502546
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Charcot-Marie-Tooth disease type 1.
    Malcolm S
    J Med Genet; 1992 Jan; 29(1):3-4. PubMed ID: 1552540
    [No Abstract]   [Full Text] [Related]  

  • 9. 3rd workshop of the European CMT consortium: 54th ENMC International Workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies 28-30 November 1997, Naarden, The Netherlands.
    Neuromuscul Disord; 1998 Dec; 8(8):591-603. PubMed ID: 10093067
    [No Abstract]   [Full Text] [Related]  

  • 10. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T; Lupo V; Martínez-Rubio D; Sancho P; Sivera R; Chumillas MJ; García-Romero M; Pascual-Pascual SI; Muelas N; Dopazo J; Vílchez JJ; Palau F; Espinós C
    Brain; 2016 Jan; 139(Pt 1):62-72. PubMed ID: 26497905
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variant.
    Querin G; Corcia P; Lenglet T; Stojkovic T; Leguern E; Cazeneuve C; Pradat PF
    Rev Neurol (Paris); 2017 Dec; 173(10):671-673. PubMed ID: 28579206
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients.
    Choi BO; Nakhro K; Park HJ; Hyun YS; Lee JH; Kanwal S; Jung SC; Chung KW
    Clin Genet; 2015 Jun; 87(6):594-8. PubMed ID: 24863639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes.
    Street VA; Meekins G; Lipe HP; Seltzer WK; Carter GT; Kraft GH; Bird TD
    Neuromuscul Disord; 2002 Oct; 12(7-8):643-50. PubMed ID: 12207932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The death panel for Charcot-Marie-Tooth panels.
    Amato AA; Reilly MM
    Ann Neurol; 2011 Jan; 69(1):1-4. PubMed ID: 21280068
    [No Abstract]   [Full Text] [Related]  

  • 16. Charcot-Marie-Tooth disease variants-classification, clinical, and genetic features and rational diagnostic evaluation.
    Bassam BA
    J Clin Neuromuscul Dis; 2014 Mar; 15(3):117-28. PubMed ID: 24534835
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the Myelin Protein Zero result in a spectrum of Charcot-Marie-Tooth phenotypes.
    Kochański A
    Acta Myol; 2004 May; 23(1):6-9. PubMed ID: 15298082
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary motor-sensory neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies. Current classification and genotype-phenotype correlation].
    Auer-Grumbach M; Wagner K; Fazekas F; Löscher WN; Strasser-Fuchs S; Hartung HP
    Nervenarzt; 1999 Dec; 70(12):1052-61. PubMed ID: 10637810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Charcot-Marie-Tooth neuropathies and related disorders.
    Mendell JR
    Semin Neurol; 1998; 18(1):41-7. PubMed ID: 9562666
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Electrodiagnostic studies in a murine model of demyelinating Charcot-Marie-Tooth disease.
    Meekins GD; Weiss MD
    Phys Med Rehabil Clin N Am; 2005 Nov; 16(4):967-79, ix. PubMed ID: 16214054
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.