Search clinical trials for: Congenital muscular torticollis
Total 21360 results
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Fondation LenvalRecruiting
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National Institutes of Health Clinical Center (CC)RecruitingCerebral Palsy | Muscular Dystrophy | Spina Bifida | Incomplete Spinal Cord InjuryUnited States
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IRCCS Policlinico S. DonatoUniversity of MilanRecruitingMarfan Syndrome | Rare Diseases | Ehlers-Danlos SyndromeItaly
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Assiut UniversityNot yet recruitingMyositis | Congenital Myopathy | Acquired Myopathy
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Hacettepe UniversityRecruitingCongenital Heart Disease | Fontan ProcedureTurkey
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Calcilytix Therapeutics, Inc., a BridgeBio companyRecruitingAutosomal Dominant Hypocalcemia (ADH)United States, Australia, United Kingdom, Denmark, Italy, France, Japan, Taiwan, Canada, Czechia, Netherlands
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University Hospital, GrenobleRecruitingArthrogryposis Multiplex Congenita (AMC)France
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Sanguine BiosciencesRecruitingHeart Diseases | Stroke | Lymphoma | Multiple Sclerosis | Kidney Diseases | Diabetes | Leukemia | Age-Related Macular Degeneration | Cancer | Arthritis | Schizophrenia | Thyroid Diseases | Parkinson Disease | Hepatitis | Vasculitis | Psoriasis | Asthma | Amyloidosis | Fibromyalgia | Graves Disease | Alzheimer Disease | Celiac Disease | Cirr... and other conditionsUnited States
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LMU KlinikumUniversity of Pisa; German Federal Ministry of Education and Research; European...RecruitingMitochondrial Diseases | MDS | Mitochondrial Myopathies | MELAS Syndrome | MIDD | Kearns-Sayre Syndrome | MERRF Syndrome | Barth Syndrome | Leigh Syndrome | MNGIE | LHON | Pearson Syndrome | NARP Syndrome | Coenzyme Q10 Deficiency | SANDO | SCAE | MIRAS | CPEOAustria, Germany, Italy
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RenJi HospitalPeking University First Hospital; Shanghai Zhongshan Hospital; First Affiliated... and other collaboratorsRecruitingKidney Cancer | Renal Cell Carcinoma | ALK Gene Mutation | MET Gene Mutation | HLRCC | Renal Tumor Histology | Cutaneous Leiomyoma | BAP1 Tumor Predisposition Syndrome | VHL Syndrome | Birt-Hogg-Dube Syndrome | Familial Renal Cancer | FLCN Gene Mutation | FH Gene Mutation | Cutaneous Leiomyomata With Uterine LeiomyomataChina
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Boston Children's HospitalRecruitingGenetic Disease | Chopra-Amiel-Gordon Syndrome | CAGS | ANKRD17United States
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University of MichiganNational Heart, Lung, and Blood Institute (NHLBI); National Institutes of Health...RecruitingObstructive Sleep Apnea | Down Syndrome | Tolerance | Trisomy 21 | Hypertonia, Muscle | Nasal Airway ObstructionUnited States
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Chinese University of Hong KongAbbottRecruitingSarcopenia | Musculoskeletal Abnormalities | Connective Tissue Diseases in Old AgeHong Kong
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Regulus Therapeutics Inc.RecruitingPolycystic Kidney, Autosomal Dominant | Autosomal Dominant Polycystic Kidney Disease | ADPKDUnited States
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University of Texas Southwestern Medical CenterCure SPG50RecruitingMicrocephaly | Spasticity, Muscle | Growth Retardation | Intellectual Deficiency | SPG50 | Spastic ParaplegiaUnited States
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University of Colorado, DenverUniversity of MarylandRecruitingPolycystic Kidney, Autosomal DominantUnited States
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Radboud University Medical CenterRecruitingAutosomal Dominant Polycystic Kidney | Polycystic Liver Disease | Liver Cyst | Autosomal Dominant Polycystic Liver DiseaseNetherlands
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Noel JabbourNational Institute on Deafness and Other Communication Disorders (NIDCD)Not yet recruitingVelopharyngeal Incompetence Due to Cleft Palate | Velopharyngeal Insufficiency | Palatopharyngeal Incompetence | Inadequate Velopharyngeal Closure | HypernasalityUnited States
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University of Erlangen-Nürnberg Medical SchoolRecruitingAutosomal Dominant Polycystic Kidney Disease | Uncontrolled Hypertension | Renal DenervationGermany
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Umeå UniversityRecruitingCongenital Heart Disease | Univentricular HeartSweden
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Dufresne, Craig, MD, PCRecruitingFreeman-Sheldon Syndrome | Whistling Face Syndrome | Freeman-Sheldon Syndrome Variant | Sheldon-Hall Syndrome | Gordon Syndrome | Arthrogryposis Distal Type 3 | Arthrogryposis Distal Type 1 | Freeman-Burian SyndromeUnited States
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Children's Hospital Medical Center, CincinnatiEunice Kennedy Shriver National Institute of Child Health and Human Development...RecruitingFragile X SyndromeUnited States
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Institut National de la Santé Et de la Recherche...RecruitingLaminopathies | Emery Dreifuss Muscular Dystrophy 2 | LMNA-Related Congenital Muscular Dystrophy | Dilated Cardiomyopathy-1AFrance
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Boston Children's HospitalBoston Children's Hospital - Children's Rare Disease Cohorts InitiativeRecruitingMovement Disorders | Neurodegenerative Diseases | Motor Neuron Disease | Spasticity, Muscle | Pediatric Disorder | Hereditary Spastic ParaplegiaUnited States
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Occlutech International ABRecruitingMuscular Ventricular Septal DefectTurkey
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Massachusetts Eye and Ear InfirmaryRecruitingParkinson Disease | Dyskinesias | Temporomandibular Joint Disorders | Dystonia | Torticollis | Essential Tremor | Tic Disorders | Dysphonia | Myoclonus | Ulnar Nerve Entrapment | Drug Induced DystoniaUnited States
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Bionano GenomicsColumbia University; University of Iowa; Medical College of Wisconsin; Augusta... and other collaboratorsRecruitingIntellectual Disability | Autism Spectrum Disorder | Fragile X Syndrome | Developmental Disability | Congenital Anomaly | Facioscapulohumeral Muscular Dystrophy 1United States
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Calcilytix Therapeutics, Inc., a BridgeBio companyRecruitingAutosomal Dominant HypocalcemiaUnited States, France, Denmark, Australia, Japan, Belgium, Canada, Italy, Netherlands, United Kingdom, Portugal, Finland, Germany
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Virginia Commonwealth UniversityRecruitingCongenital Myotonic Dystrophy | Childhood Myotonic Dystrophy | CDM | CHDMUnited States, Italy
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Institut de Myologie, FranceRecruitingMuscular Dystrophies | Mitochondrial Myopathies | Glycogen Storage Disease | Idiopathic Inflammatory Myopathies | Congenital MyopathyFrance
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Institut de Myologie, FranceRecruitingMuscular Dystrophies | Mitochondrial Myopathies | Glycogen Storage Disease | Idiopathic Inflammatory Myopathies | Congenital MyopathyFrance
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Xuanwu Hospital, BeijingRecruitingGait | Motor FunctionChina
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University of BernUniversity Hospital Inselspital, Berne; University of Lausanne Hospitals; University... and other collaboratorsRecruitingCongenital Muscular Dystrophy | SMA | DMD | BMD | IMDSwitzerland
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Tasly GeneNet Pharmaceuticals Co., LtdRecruitingCharcot-Marie-Tooth Type 1AChina
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Medical University of GdanskRecruitingMuscular Dystrophy, DuchennePoland
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Assistance Publique - Hôpitaux de ParisRecruitingLung Diseases | Neuromuscular Diseases | Scoliosis | Congenital Diaphragmatic Hernia | Cardiac Diseases | Diaphragmatic Impairment | Respiratory Muscle ImpairmentFrance
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AMO Pharma LimitedRecruitingCongenital Myotonic DystrophyUnited States, Canada, Australia, New Zealand
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Boston Children's HospitalAcademy of Nutrition and DieteticsRecruitingCongenital Heart Disease | ICU Acquired Weakness | Catabolic StateUnited States
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University Health Network, TorontoRecruitingHypermobile EDS (hEDS) | Hypermobility SyndromeCanada
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Peking University Third HospitalRecruiting
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James DowlingCanadian Institutes of Health Research (CIHR); Cures Within Reach; The Joshua... and other collaboratorsRecruitingX Linked Myotubular MyopathyUnited Kingdom, Canada, United States
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University of MiamiNational Institute of Neurological Disorders and Stroke (NINDS); National Institutes...RecruitingAmyotrophic Lateral Sclerosis | Primary Lateral Sclerosis | Frontotemporal Dementia | Progressive Muscular Atrophy | Hereditary Spastic ParaplegiaUnited States, South Africa
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Medical University of SilesiaRecruiting
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Thomas Jefferson UniversityRecruitingStroke | Cerebral Palsy | Amyotrophic Lateral Sclerosis | Muscular Dystrophies | Spinal Cord Injuries | Hemiparesis | Spinal Muscular Atrophy | Quadriplegia | Arthrogryposis | Neurologic Diseases | Charcot-Marie-Tooth | Weakness of Extremities as Sequela of Stroke | Weakness Due to Upper Motor Neuron Dysfunction | Arm ParalysisUnited States
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Simone Spuler, MDGerman Federal Ministry of Education and ResearchNot yet recruitingUrinary Incontinence | Epispadias, MaleGermany
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Boston Children's HospitalCureAP4 FoundationRecruitingHereditary Spastic Paraplegia | SPG50 | SPG47 | SPG51 | SPG52 | AP4-related Hereditary Spastic Paraplegia | Early Onset Hereditary Spastic Paraplegia | SPG4 | SPG3A | SPG15 | SPG11United States
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Centro Universitário Augusto MottaRecruitingQuality of Life | Physical Activity | Exercise | Sickle Cell Anemia | Muscle DysfunctionBrazil
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National Medical Research Center for Therapy and...Moscow State University of Medicine and DentistryRecruitingMedication Adherence | Adherence, Medication | Treatment Adherence | Familial Hypercholesterolemia | Motivational Interviewing | Adherence, Patient | Treatment Adherence and Compliance | Patient Compliance | Adherence | Hypercholesterolemia, Familial | Patient Adherence | Hypercholesterolemia, Autosomal Dominant and other conditionsRussian Federation
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Stanford UniversityAmerican Diabetes AssociationRecruiting
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Tongji HospitalNanjing IASO Biotechnology Co., Ltd.RecruitingMultiple Sclerosis | Autoimmune Diseases of the Nervous System | Autoimmune Diseases | Myasthenia Gravis | Neuromyelitis Optica Spectrum Disorder | Autoimmune Encephalitis | Idiopathic Inflammatory Myopathies | Chronic Inflammatory Demyelinating Polyradiculoneuropathy | Myelin Oligodendrocyte Glycoprotein... and other conditionsChina