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 *

221 related articles for article (PubMed ID: 21498094)

  • 1. Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes.
    Barišić N; Chaouch A; Müller JS; Lochmüller H
    Eur J Paediatr Neurol; 2011 May; 15(3):189-96. PubMed ID: 21498094
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment.
    Engel AG; Shen XM; Selcen D; Sine SM
    Lancet Neurol; 2015 Apr; 14(4):420-34. PubMed ID: 25792100
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital myasthenic syndromes: phenotypic expression and pathophysiological characterisation].
    Andreux F; Hantaï D; Eymard B
    Rev Neurol (Paris); 2004 Feb; 160(2):163-76. PubMed ID: 15034473
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital myasthenic syndromes in 2012.
    Engel AG
    Curr Neurol Neurosci Rep; 2012 Feb; 12(1):92-101. PubMed ID: 21997714
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. 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]  

  • 8. Animal Models of the Neuromuscular Junction, Vitally Informative for Understanding Function and the Molecular Mechanisms of Congenital Myasthenic Syndromes.
    Webster RG
    Int J Mol Sci; 2018 Apr; 19(5):. PubMed ID: 29710836
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

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

  • 11. Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes.
    Beeson D; Webster R; Ealing J; Croxen R; Brownlow S; Brydson M; Newsom-Davis J; Slater C; Hatton C; Shelley C; Colquhoun D; Vincent A
    Ann N Y Acad Sci; 2003 Sep; 998():114-24. PubMed ID: 14592868
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Current status of the congenital myasthenic syndromes.
    Engel AG
    Neuromuscul Disord; 2012 Feb; 22(2):99-111. PubMed ID: 22104196
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 15. Congenital myasthenic syndromes and the formation of the neuromuscular junction.
    Beeson D; Webster R; Cossins J; Lashley D; Spearman H; Maxwell S; Slater CR; Newsom-Davis J; Palace J; Vincent A
    Ann N Y Acad Sci; 2008; 1132():99-103. PubMed ID: 18567858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up.
    Durmus H; Shen XM; Serdaroglu-Oflazer P; Kara B; Parman-Gulsen Y; Ozdemir C; Brengman J; Deymeer F; Engel AG
    Neuromuscul Disord; 2018 Apr; 28(4):315-322. PubMed ID: 29395675
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation.
    Yasaki E; Prioleau C; Barbier J; Richard P; Andreux F; Leroy JP; Dartevelle P; Koenig J; Molgó J; Fardeau M; Eymard B; Hantaï D
    Neuromuscul Disord; 2004 Jan; 14(1):24-32. PubMed ID: 14659409
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic basis and phenotypic features of congenital myasthenic syndromes.
    Engel AG
    Handb Clin Neurol; 2018; 148():565-589. PubMed ID: 29478601
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sleuthing molecular targets for neurological diseases at the neuromuscular junction.
    Engel AG; Ohno K; Sine SM
    Nat Rev Neurosci; 2003 May; 4(5):339-52. PubMed ID: 12728262
    [No Abstract]   [Full Text] [Related]  

  • 20. Therapeutic strategies for congenital myasthenic syndromes.
    Lee M; Beeson D; Palace J
    Ann N Y Acad Sci; 2018 Jan; 1412(1):129-136. PubMed ID: 29381222
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.