Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Condition:   Myotubular MyopathyIntervention:   Sponsors:   Valerion Therapeutics, LLC;   Institut de Myologie, France;   GenethonRecruiting - verified February 2014 (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - February 4, 2014 Category: Research Source Type: clinical trials

Prospective, Longitudinal Study of the Natural History and Functional Status of Patients With Myotubular Myopathy (MTM)
Condition:   Myotubular MyopathyIntervention:   Sponsors:   Valerion Therapeutics, LLC;   Institut de Myologie, France;   GenethonRecruiting - verified April 2014 (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - February 4, 2014 Category: Research Source Type: clinical trials

Myotubular Myopathy Genetic Testing Study
Condition:   Myotubular MyopathyIntervention:   Other: Genetic TestingSponsors:   Cure CMD;   Valerion Therapeutics, LLC;   Congenital Muscle Disease International Registry (CMDIR);   University of Chicago;   Children's Hospital BostonRecruiting - verified February 2015 (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - March 19, 2013 Category: Research Source Type: clinical trials

Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Conditions:   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 ...
Source: ClinicalTrials.gov - July 26, 2011 Category: Research Source Type: clinical trials

Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Conditions:   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 ...
Source: ClinicalTrials.gov - July 26, 2011 Category: Research Source Type: clinical trials