Page 1 of Clinical Trials for "Muscular Dystrophies, Limb-Girdle", 12 Total Matches
- 1Active, not recruitingLast Updated: March 11, 2012Condition(s): Becker Muscular Dystrophy; Limb-Girdle Muscular Dystrophy, Type 2A; Calpain-3 Deficiency; Limb-Girdle Muscular Dystrophy, Type 2B; Miyoshi Myopathy; Dysferlin Deficiency; Limb-Girdle Muscular Dystrophy, Type 2I; FKRP-deficiency
- 2CompletedLast Updated: April 28, 2011Condition(s): Limb Girdle Muscular Dystrophy Type 2C; Gamma-sarcoglycanopathy
- 3Active, not recruitingLast Updated: April 10, 2012Condition(s): Limb-Girdle Muscular Dystrophy
- 4CompletedLast Updated: March 22, 2012Condition(s): Muscular Dystrophies
- 5Active, not recruitingLast Updated: July 29, 2011Condition(s): Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Limb Girdle Muscular Dystrophy
- 6CompletedLast Updated: October 26, 2011Condition(s): Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Limb Girdle Muscular Dystrophy
- 7RecruitingLast Updated: November 15, 2011Condition(s): Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Limb Girdle Muscular Dystrophy
- 8RecruitingLast Updated: July 21, 2011Condition(s): Limb-girdle Muscular Dystrophy; Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Facioscapulohumeral Muscular Dystrophy
- 9CompletedLast Updated: December 19, 2007Condition(s): Becker Muscular Dystrophy; Facioscapulohumeral Muscular Dystrophy; Limb-Girdle Muscular Dystrophy
- 10RecruitingLast Updated: July 31, 2009Condition(s): Muscular Dystrophies; Becker Muscular Dystrophy; Limb-Girdle Muscular Dystrophy
- 11RecruitingLast Updated: July 28, 2011Condition(s): Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; 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 Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy
- 12CompletedLast Updated: January 27, 2009Condition(s): LGMD2B; Miyoshi Myopathy; Dysferlinopathy
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The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Muscular+Dystrophies%2C+Limb-Girdle%22
