Find NINDS Clinical Trials

Find NINDS Clinical Trials

Subscribe to Find NINDS Clinical TrialsRSS
Filter By:
Returning 70 results
Study Titlesort descending Location Status Disorders
Study of GABA-A Receptors in the Generation of Tics in Patients With Tourette's Syndrome Maryland* Completed Tourette Syndrome
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes Texas Completed Williams Syndrome, Angelman Syndrome, Prader-Willi Syndrome, Shprintzen Syndrome, Smith-Magenis Syndrome, DiGeorge Syndrome, Chromosome Abnormalities
Study of Psychological and Motor Effects of Testosterone in Adolescents With XXY/Klinefelter Syndrome Colorado Completed Klinefelter Syndrome, XXY Syndrome
Study of Tics in Patients With Tourette's Syndrome and Chronic Motor Tic Disorder Maryland* Completed Tourette Syndrome, Tic Disorders
The Effect of Androgen and Growth Hormone on Height and Learning in Girls With Turner Syndrome Multiple U.S. Locations Completed Turner Syndrome
The Myelin Disorders Biorepository Project Multiple U.S. Locations Recruiting Leukodystrophy, White Matter Disease, Leukoencephalopathies, Aicardi Goutieres Syndrome, Metachromatic Leukodystrophy, TUBB4A-Related Leukodystrophy, 4H Syndrome, Krabbe Disease, Alexander Disease, Pelizaeus-Merzbacher Disease, Adrenoleukodystrophy, Adrenomyeloneuropathy, Multiple Sulfatase Deficiency, Megalencephalic Leukoencephalopathy With Subcortical Cysts, Vanishing White Matter Disease, Cockayne Syndrome, Labrune Syndrome, ADLD, Gangliosidoses, Peroxisomal Biogenesis Disorder, Adult-Onset Leukodystrophy With Neuroaxonal Spheroids, Hereditary Diffuse Leukoencephalopathy With Spheroids
Timing of Voluntary Movement in Patients With Tourette Syndrome and Chronic Tic Disorder Maryland* Completed Tourette Syndrome, Tic Disorders
Topiramate for Cryptogenic Sensory Peripheral Neuropathy in Metabolic Syndrome (CSPN) Multiple U.S. Locations Active, Not Recruiting Cryptogenic Sensory Peripheral Neuropathy in Metabolic Syndrome
Treatment Development of Triheptanoin (G1D) Texas Not Yet Recruiting Epilepsy, GLUT1DS1, Glut1 Deficiency Syndrome 1, Autosomal Recessive, Glucose Metabolism Disorders, Glucose Transport Defect, Glucose Transporter Type 1 Deficiency Syndrome, Glucose Transporter Protein Type 1 Deficiency Syndrome
Trial of Sirolimus for Cognitive Impairment in Sturge-Weber Syndrome Multiple U.S. Locations Recruiting Sturge-Weber Syndrome

Pages