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 *

242 related articles for article (PubMed ID: 23995276)

  • 1. Congenital myasthenic syndromes: an update.
    Hantaï D; Nicole S; Eymard B
    Curr Opin Neurol; 2013 Oct; 26(5):561-8. PubMed ID: 23995276
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital myasthenic syndromes.
    Eymard B; Hantaï D; Estournet B
    Handb Clin Neurol; 2013; 113():1469-80. PubMed ID: 23622369
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital myasthenic syndromes: spotlight on genetic defects of neuromuscular transmission.
    Müller JS; Mihaylova V; Abicht A; Lochmüller H
    Expert Rev Mol Med; 2007 Aug; 9(22):1-20. PubMed ID: 17686188
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited disorders of the neuromuscular junction: an update.
    Rodríguez Cruz PM; Palace J; Beeson D
    J Neurol; 2014 Nov; 261(11):2234-43. PubMed ID: 25305004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital myasthenic syndrome: a brief review.
    Lorenzoni PJ; Scola RH; Kay CS; Werneck LC
    Pediatr Neurol; 2012 Mar; 46(3):141-8. PubMed ID: 22353287
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital Myasthenic Syndromes.
    Iyadurai SJP
    Neurol Clin; 2020 Aug; 38(3):541-552. PubMed ID: 32703467
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital myasthenic syndromes and the neuromuscular junction.
    Rodríguez Cruz PM; Palace J; Beeson D
    Curr Opin Neurol; 2014 Oct; 27(5):566-75. PubMed ID: 25159927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Congenital myasthenic syndromes; French experience].
    Eymard B; Hantaï D; Fournier E; Nicole S; Sternberg D; Richard P; Fardeau M
    Bull Acad Natl Med; 2014 Feb; 198(2):257-70; discussion 270-1. PubMed ID: 26263703
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital myasthenic syndromes.
    Engel AG
    Handb Clin Neurol; 2008; 91():285-331. PubMed ID: 18631848
    [No Abstract]   [Full Text] [Related]  

  • 10. Congenital myasthenic syndromes.
    Hantaï D; Richard P; Koenig J; Eymard B
    Curr Opin Neurol; 2004 Oct; 17(5):539-51. PubMed ID: 15367858
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience].
    Eymard B; Stojkovic T; Sternberg D; Richard P; Nicole S; Fournier E; Béhin A; Laforêt P; Servais L; Romero N; Fardeau M; Hantaï D;
    Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S45-55. PubMed ID: 23452772
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital myasthenic syndromes.
    Harper CM
    Semin Neurol; 2004 Mar; 24(1):111-23. PubMed ID: 15229798
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital Myasthenic Syndromes in 2018.
    Engel AG
    Curr Neurol Neurosci Rep; 2018 Jun; 18(8):46. PubMed ID: 29892917
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The congenital myasthenic syndromes: expanding genetic and phenotypic spectrums and refining treatment strategies.
    Vanhaesebrouck AE; Beeson D
    Curr Opin Neurol; 2019 Oct; 32(5):696-703. PubMed ID: 31361628
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable].
    Wunderlich G; Abicht A; Brunn A; Daimagüler HS; Schroeter M; Fink GR; Lehmann HC; Cirak S
    Nervenarzt; 2019 Feb; 90(2):148-159. PubMed ID: 29974128
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and research strategies for limb-girdle congenital myasthenic syndromes.
    O'Connor E; Töpf A; Zahedi RP; Spendiff S; Cox D; Roos A; Lochmüller H
    Ann N Y Acad Sci; 2018 Jan; 1412(1):102-112. PubMed ID: 29315608
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital myasthenic syndromes: current diagnostic and therapeutic approaches.
    Schara U; Della Marina A; Abicht A
    Neuropediatrics; 2012 Aug; 43(4):184-93. PubMed ID: 22911480
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmission.
    Nicolau S; Liewluck T; Shen XM; Selcen D; Engel AG; Milone M
    Neuromuscul Disord; 2019 Aug; 29(8):614-617. PubMed ID: 31378432
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes.
    Rodríguez Cruz PM; Palace J; Beeson D
    Int J Mol Sci; 2018 Jun; 19(6):. PubMed ID: 29874875
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital myasthenic syndromes: recent advances.
    Beeson D
    Curr Opin Neurol; 2016 Oct; 29(5):565-71. PubMed ID: 27472506
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.