Search clinical trials for: congenital fiber type disproportion
Total 74039 results
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Boston Children's HospitalMuscular Dystrophy AssociationRecruitingCentronuclear Myopathy | Myotubular Myopathy | Nemaline Myopathy | Central Core Disease | Congenital Fiber Type Disproportion | Multiminicore Disease | Rigid Spine Muscular Dystrophy | Undefined Congenital MyopathyUnited States
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RWTH Aachen UniversityDLR German Aerospace CenterRecruitingPostural Tachycardia Syndrome | Autonomic Neuropathy | Small Fiber Neuropathy | Ehlers-Danlos Syndrome Hypermobility TypeGermany
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Aalborg University HospitalAalborg UniversityEnrolling by invitationDiabetes | Diabetes Mellitus, Type 1 | Diabetic Neuropathy Peripheral | Small Fiber NeuropathyDenmark
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NMD Pharma A/SAarhus University Hospital; Ohio State UniversityCompletedCharcot-Marie-Tooth DiseaseUnited States, Denmark
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Agricultural University of AthensCompletedAppetitive Behavior | Potential Abnormality of Glucose ToleranceGreece
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Radboud University Medical CenterNot yet recruitingADHD - Combined Type | Kbg Syndrome
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Inozyme PharmaNot yet recruitingPseudoxanthoma Elasticum | Arterial Calcification | Gene Mutations | Ectonucleotide Pyrophosphatase/phosphodiesterase1 Deficiency | Autosomal Recessive Hypophosphatemic Rickets Type 2
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West China HospitalRecruitingLymphatic MalformationChina
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QED Therapeutics, Inc.RecruitingHypochondroplasiaUnited States, Australia, Norway, Portugal, Singapore, Spain, Canada, France, Germany, Sweden, United Kingdom
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Peking University First HospitalRecruitingRenal Cell Carcinoma | VHL SyndromeChina
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GRIN Therapeutics, Inc.RecruitingTuberous Sclerosis Complex | Focal Cortical DysplasiaSpain, United Kingdom, Australia, Belgium, Canada, Italy, Poland
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IRCCS Eugenio MedeaRecruiting
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Cairo UniversityNot yet recruitingMolar Incisor Hypomineralization
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University of MichiganRecruitingHeart Failure With Preserved Ejection Fraction | Type2diabetesUnited States
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National University Hospital, SingaporeRecruiting
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Maastricht University Medical CenterRecruitingQuality of Life | Tuberous Sclerosis | Basal Cell Nevus Syndrome | Cutis Laxa | Epidermolysis Bullosa | Ichthyosis | Ectodermal Dysplasia | Albinism | Birt-Hogg-Dube Syndrome | Palmoplantar KeratosesNetherlands
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ENCellRecruitingCharcot-Marie-Tooth Disease Type 1AKorea, Republic of
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Bark Technology LLPRecruitingCardiac Surgical Patients (CABG,Mammary Coronary Bypass Surgery,Plastic and Replacement of Valves, Atrial Septal Defect,Ventricular Septal Defect)Kazakhstan
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Inozyme PharmaGACI GlobalNot yet recruitingATP-Binding Cassette Subfamily C Member 6 Deficiency | Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 Deficiency
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Nanjing Children's HospitalRecruiting
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Joyce TengStanford UniversityNot yet recruiting
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Yang TaoNot yet recruitingType 1 Diabetes | Diet Intervention | Glucose Control
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Central Hospital, Nancy, FranceRecruiting
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Cure HHTUniversity of Colorado, Denver; Massachusetts General Hospital; Mayo Clinic; Children... and other collaboratorsRecruitingArteriovenous Malformations | Epistaxis | Hereditary Hemorrhagic Telangiectasia | GastroIntestinal Bleeding | Telangiectasia | Vascular Malformation | Cerebral Arteriovenous MalformationsUnited States
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University of Eastern FinlandRecruitingOverweight and Obesity | Postprandial Hyperglycemia | Type2diabetesFinland
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Hospital Universitari Vall d'Hebron Research InstituteERN-EuroBloodNet (European Reference Network on Rare Hematological DiseasesRecruitingLeukemia | Anemia | Iron Metabolism Disorders | Anemia, Sickle Cell | Thalassemia | Bleeding Disorder | Myeloma | Lymphoid Neoplasm | Blood Cancer | Bone Marrow Failure | Red Cell Membrane and Enzyme Abnormalities | Myeloma, MalignantSpain
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Hama UniversityRecruitingMalocclusion, Angle's ClassSyrian Arab Republic
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Palvella Therapeutics, Inc.Not yet recruitingMicrocystic Lymphatic MalformationUnited States
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Zdeněk ŠumníkRecruiting
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Samsung Medical CenterNot yet recruitingCharcot-Marie-Tooth Disease, Type 1
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Beijing Tiantan HospitalBeijing Friendship Hospital; RenJi Hospital; Qilu Hospital of Shandong University and other collaboratorsRecruitingHemangioma, Cavernous, Central Nervous SystemChina
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aya ramadan ashmawy sarhanNot yet recruiting
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Children's Hospital of Fudan UniversityAdfontes (Shanghai) Bio-technology Co.,Ltd.Recruiting
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IRCCS San RaffaeleUniversità Vita-Salute San RaffaeleRecruitingCarcinoma, Renal Cell | Von Hippel-Lindau DiseaseItaly
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IRCCS San RaffaeleRecruitingClear Cell Renal Cell Carcinoma | VHL SyndromeItaly
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University Hospital, Strasbourg, FranceRecruitingMaxillofacial AbnormalitiesFrance
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David M. RitterRecruitingTuberous Sclerosis Complex | LymphangioleiomyomatosisUnited States
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Sohag UniversityRecruitingVascular Malformations | Microcystic Lymphatic Malformation | Combined Vascular MalformationEgypt
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Elpida Therapeutics SPCNot yet recruitingNeuromuscular Diseases | Peripheral Neuropathy | Neuro-Degenerative Disease
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University Hospital, GrenobleRecruiting
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Mayo ClinicNational Heart, Lung, and Blood Institute (NHLBI)RecruitingHigh Blood Pressure | Coarctation of AortaUnited States
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NYU Langone HealthNot yet recruitingFamilial DysautonomiaUnited States
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Assistance Publique - Hôpitaux de ParisNot yet recruitingHemophilia A | Hemophilia B | Cystic Fibrosis | Sickle Cell Disease | Muscular Dystrophy, Duchenne | Fragile X Syndrome | Huntington Disease | Myotonic Dystrophy | Autosomal Recessive Polycystic Kidney Disease | Neurofibromatosis-Noonan Syndrome | Muscular Dystrophy, Becker | Invasive PreNatal Diagnosis in a... and other conditionsFrance
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Motric BioRecruitingStroke | Multiple Sclerosis | Cerebral Palsy | Spinal Cord Injuries | Dystonia | Muscle Spasticity | Hereditary Spastic Paraplegia | Hypertonia, MuscleUnited States
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University College, LondonRecruitingHereditary Sensory Neuropathy Type IUnited Kingdom
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Hospices Civils de LyonNot yet recruitingLowry Wood Syndrome | Roifman Syndrome | Taybi Linder Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism Types I and IIIFrance
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University Health Network, TorontoRecruitingArteriovenous MalformationsCanada
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National Human Genome Research Institute (NHGRI)RecruitingMetabolic Disease | Purine-Pyrimidine Metabolism | AICDA, OMIM *605257, Immunodeficiency With Hyper-IgM, Type 2; HIGM2 | UNG, OMIM *191525, Hyper-IgM Syndrome 5 | NT5C3A<TAB>, OMIM *606224, Anemia, Hemolytic, Due to UMPH1 Deficiency | UMPS, OMIM *613891, Orotic Aciduria | DHODH, OMIM *126064,... and other conditionsUnited States
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University Hospital PadovaRecruitingHypertension | Essential Hypertension | Hyperaldosteronism | Aldosteronism | Conn Adenoma | Aldosterone Disorder | Aldosterone-producing Adenoma | Bilateral Adrenal HyperplasiaItaly
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Anagnostou, Evdokia, M.D.The Hospital for Sick Children; Canadian Institutes of Health Research (CIHR); Alberta Health services and other collaboratorsNot yet recruitingAnxiety Disorders | Generalized Anxiety Disorder | Anxiety | Tuberous Sclerosis | ADHD | Neurodevelopmental Disorders | Autism Spectrum Disorder | Fragile X Syndrome | Social Anxiety | Social Anxiety Disorder | Agoraphobia | Tourette Syndrome | Tic Disorders | Autism | ADHD Predominantly Inattentive Type | ADHD - Combined... and other conditionsCanada