Clinical Trials on Bethlem Myopathy

Total 5 results

  • NCT04020159
    Recruiting
    Conditions: Bethlem Myopathy, Ullrich Congenital Muscular Dystrophy 1, Digenic, Col6A1/Col6A2, Ullrich Congenital Muscular Dystrophy 1, Autosomal Recessive, Ullrich Congenital Muscular Dystrophy 1, Autosomal Dominant, Bethlem Myopathy 1, Autosomal Recessive, UCMD, BTHLM1
  • NCT03693898
    Unknown status
    Conditions: Bethlem Myopathy, Ullrich Disease
  • NCT01403402
    Unknown status
    Conditions: Congenital Muscular Dystrophy (Including Unspecified/Undiagnosed), Dystroglycanopathy, Congenital Fiber Type Disproportion, Rigid Spine Muscular Dystrophy, Congenital Myopathy (Including Unspecified/Undiagnosed), Collagen VI CMD (Ullrich CMD, Intermediate, Bethlem Myopathy), Laminin Alpha 2 Related Congenital Muscular Dystrophy, LAMA2-CMD/Merosin Deficient/MDC1A, Walker-Warburg Syndrome, Muscle-Eye-Brain Disease, Fukuyama/Fukutin Related Muscular Dystrophy, Integrin Alpha 7 Deficiency, Integrin Alpha 9 Deficiency, LMNA-CMD/Lamin A/C/Laminopathy, SEPN1-Related Myopathy, Bethlem Myopathy, Actin Aggregation Myopathy, Cap Disease, Central Core Disease, Centronuclear Myopathy, Core Rod Myopathy, Hyaline Body Myopathy, Multiminicore Myopathy, Myotubular Myopathy, Nemaline Myopathy, Tubular Aggregate Myopathy, Zebra Body Myopathy, Reducing Body Myopathy, Spheroid Body Myopathy, LGMD1B (LMNA), LGMD1E (DES), LGMD2G (TCAP), LGMD2H (TRIM32), LGMD2I (FKRP), LGMD2J (TTN), LGMD2K (POMT1), LGMD2M (FKTN), LGMD2N (POMT2), LGMD2O (POMGnT1), LGMD2P (DAG1), LGMD2Q (PLEC1), LGMD2R (DES), LGMD2S (TRAPPC11), LGMD2T (GMPPB), LGMD2U (ISPD), LGMD2V (GAA), Ullrich Congenital Muscular Dystrophy, Titinopathy, Choline Kinase B Receptor, Emery-Dreifuss Muscular Dystrophy, RYR1 Related Myopathy, SYNE1/Nesprin Related Muscular Dystrophy, Telethonin Related Muscular Dystrophy (TCAP/Titin-Cap), Congenital Myasthenic Syndrome, Escobar Syndrome, Myofibrillar Myopathy, Malignant Hyperthermia, Alpha-Dystroglycan Related Muscular Dystrophy (DAG1, DPM1, DPM2, DPM3, FKRP, FKTN), Alpha-Dystroglycan Related Muscular Dystrophy (GAA, ISPD, LARGE, POMT1, POMT2, POMGnT1), Alpha-Dystroglycan Related Muscular Dystrophy (Unspecified/Undiagnosed/Other)
  • NCT01438788
    Completed
    Conditions: Bethlem Myopathy, Ullrich Congenital Muscular Dystrophy
  • NCT01895283
    Completed
    Conditions: Bethlem Myopathy