NCT02422732
- Conditions
- Communication Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslexia, +25 more
- Locations
-
- CHU Toulouse Toulouse, France
Clinical trial condition
Heredodegenerative Disorders, Nervous System
Explore clinical trials studying Heredodegenerative Disorders, Nervous System. Study availability and eligibility vary by location and protocol.
1,877 public trials
411 recruiting studies
Heredodegenerative Disorders, Nervous System trial results
NCT01493973
- Conditions
- Ataxia, Brain Diseases, Central Nervous System Diseases, +16 more
- Locations
-
- Università di Bari Bari, BA, Italy
- Università la Sapienza, Neurologia C Rome, RM, Italy
- Dipartimento di Scienze Neurologiche Naples, Italy
Completed
Activity in Tourette Syndrome
NCT02153463
- Conditions
- Basal Ganglia Diseases, Behavior, Brain Diseases, +13 more
- Locations
-
- Children's Hospital of Eastern Ontario Ottawa, Ontario, Canada
NCT01357681
- Conditions
- Basal Ganglia Diseases, Behavior, Brain Diseases, +14 more
- Locations
-
- Department of Neuropsychiatry Berlin, Germany
- Neurologische Klinik der Ruhr-Universität Bochum Bochum, Germany
- Universitätsklinikum Ulm, Klinik für Neurologie Ulm, Germany
Completed
CARNIVAL Type I: Valproic Acid and Carnitine in Infants With Spinal Muscular Atrophy (SMA) Type I
NCT00661453
- Conditions
- Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +9 more
- Locations
-
- Johns Hopkins University Baltimore, Maryland, United States
- Children's Hospital of Michigan Detroit, Michigan, United States
- Duke University Medical Center Durham, North Carolina, United States
- Ohio State University Medical Center, Dept. of Neurology Columbus, Ohio, United States
NCT00497159
- Conditions
- Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +14 more
- Locations
-
- Huntington Study Group Rochester, New York, United States
NCT00851461
- Conditions
- Bulbo-Spinal Atrophy, X-Linked, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
- Locations
-
- Medical Genetics and Molecular Medicine Unit,, Department of Medicine, Ramathibodi Hospital Bangkok, Thailand
NCT00357669
- Conditions
- Brain Diseases, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +16 more
- Locations
-
- Kuopio, Finland
- Tampere, Finland
- Marseille, France
- Montpellier, France
Completed
Relations Between Myotonia and Fitness
NCT02161835
- Conditions
- Behavior, Congenital Myotonia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Neuromuscular Research Unit, Department of Neurology, Rigshospitalet Copenhagen, Denmark
NCT02020187
- Conditions
- Behavior, Congenital Myopathy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Neuromuscular Research Unit Copenhagen, Denmark