Ensayos clínicos sobre Síndrome miasténico de Lambert-Eaton

Total 22 resultados





    • NCT02970162
      Completado
      Condiciones: Lambert-Eaton Myasthenic Syndrome
    • NCT01373333
      No longer available
      Condiciones: Lambert-Eaton Myasthenic Syndrome
    • NCT01377922
      Completado
      Condiciones: Lambert Eaton Myasthenic Syndrome
    • NCT00994916
      No longer available
      Condiciones: Lambert-Eaton Myasthenic Syndrome
    • NCT01378546
      No longer available
      Condiciones: Lambert Eaton Myasthenic Syndrome (LEMS)
    • NCT01511978
      Completado
      Condiciones: Lambert-Eaton Myasthenic Syndrome; Eaton-Lambert Myasthenic Syndrome
    • NCT00704925
      No longer available
      Condiciones: Lambert Eaton Myasthenic Syndrome
    • NCT01825395
      Available
      Condiciones: Lambert Eaton Myasthenic Syndrome
    • NCT00872950
      Activo, no reclutando
      Condiciones: Lambert-Eaton Myasthenic Syndrome; Congenital Myasthenic Syndrome
    • NCT03062631
      Available
      Condiciones: Congenital Myasthenic Syndrome; Lambert-Eaton Myasthenic Syndrome
    • NCT00004832
      Completado
      Condiciones: Lambert-Eaton Myasthenic Syndrome
    • NCT02012933
      No longer available
      Condiciones: Lambert-Eaton Myasthenic Syndrome (LEMS); Congenital Myasthenia (CM)
    • NCT01203592
      Completado
      Condiciones: Congenital Myasthenic Syndrome
    • NCT02189720
      No longer available
      Condiciones: Congenital Myasthenic Syndrome
    • NCT02562066
      Completado
      Condiciones: Myasthenic Syndromes, Congenital
    • NCT01765140
      No longer available
      Condiciones: Myasthenic Syndromes, Congenital
    • NCT01474980
      Completado
      Condiciones: Congenital Myasthenic Syndrome
    • NCT00541216
      Estado desconocido
      Condiciones: Myasthenic Syndromes, Congenital
    • NCT02090725
      Terminado
      Condiciones: Muscle Weakness
    • NCT02124616
      Reclutamiento
      Condiciones: Spinal Muscular Atrophy; Muscular Dystrophy; Muscle Diseases; Myasthenic Syndromes; Polyneuropathies
    • NCT00716066
      Reclutamiento
      Condiciones: Autoimmune Disease; Neurologic Autoimmune Disease; Autologous Transplant Autoimmune; Multiple Sclerosis Transplant; MS Stem Cell Transplant; Multiple Sclerosis Stem Cell Transplant; Stiff Person Syndrome; HCT for Neurologic Autoimmune Disorders; CIDP Transplant; Myasthenia Gravis Transplant; Autoimmune Nervous System Disorder; Central Nervous System Vasculitis; Cerebellar Degeneration; Chronic Inflammatory Demyelinating Polyneuropathy; Lambert Eaton Myasthenic Syndrome; Myasthenia Gravis; Neuromyelitis Optica; Opsoclonus Myoclonus Syndrome; Rasmussen Subacute Encephalitis
    • NCT01403402
      Estado desconocido
      Condiciones: 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)