Centronuclear Myopathies Clinical Trials This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.
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