Clinical Trials

Stress Disorders, Post-Traumatic

Pediatric acute-onset neuropsychiatric syndrome, Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections, Brain Injuries, Traumatic, Phobia, Social, Post-Lyme Disease Syndrome, Avoidant Restrictive Food Intake Disorder, Mast Cell Activation Syndrome, Neuroinflammatory Diseases, Psychological Well-Being, Post-Acute COVID-19 Syndrome, Generalized Anxiety Disorder, Anorexia Nervosa, Anxiety Disorders, Arthritis, Juvenile, Autoimmune Diseases, Autonomic Nervous System Diseases, Mental Disorders, Celiac Disease, Colitis, Ulcerative, Combat Disorders, Crohn Disease, Depression, Ehlers-Danlos Syndrome, Encephalitis, Endometriosis, Fatigue, Mental Fatigue, Fibromyalgia, Tourette Syndrome, Migraine Disorders, Multiple Sclerosis, Myasthenia Gravis, Narcolepsy, Obsessive-Compulsive Disorder, Psoriasis, Rheumatic Fever, Spondylitis, Ankylosing, Stress Disorders, Post-Traumatic, Inflammatory Bowel Diseases, Arthritis, Psoriatic, Fatigue Syndrome, Chronic, Mood Disorders, Autoimmune Diseases of the Nervous System, Bulimia Nervosa, Postural Orthostatic Tachycardia Syndrome

Uterine Cervical Neoplasms, Stress Disorders, Post-Traumatic

Severe combined immunodeficiency due to adenosine deaminase deficiency, 3-methylcrotonyl CoA carboxylase 1 deficiency, 3-methylcrotonyl CoA carboxylase 2 deficiency, 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Ataxia with vitamin E deficiency, Beta ketothiolase deficiency, Bile acid synthesis defect, congenital, 2, Carnitine palmitoyl transferase 1A deficiency, Carnitine palmitoyl transferase 2 deficiency, Creatine deficiency, X-linked, Adrenocorticotropic hormone deficiency, Maple syrup urine disease, type 1A, Maple syrup urine disease, type 1B, Maple syrup urine disease, type 2, Congenital disorder of glycosylation type 1B, Medium chain acyl CoA dehydrogenase deficiency, N-acetyl glutamate synthetase deficiency, Niemann-Pick disease, type C2, Pyridoxine-dependent epilepsy, VLCAD deficiency, Primary hyperoxaluria type 1, Primary hyperoxaluria type 2, Waardenburg syndrome type 2, Waardenburg syndrome type 2A, Usher syndrome, type 1B, Usher syndrome, type 1C, Usher syndrome, type 1F, Amaurosis congenita of Leber, type 2, Glut1 Deficiency Syndrome, Glutaric Acidemia I, Glutathione synthetase deficiency, Brown-Vialetto-Van Laere syndrome, Methylenetetrahydrofolate reductase deficiency, Methylmalonic acidemia with homocystinuria, Methylmalonic aciduria cblA type, Methylmalonic aciduria cblB type, Pitt-Hopkins syndrome, Stickler syndrome, type 1, Stickler syndrome, type 2, Segawa syndrome, autosomal recessive, Guanidinoacetate methyltransferase deficiency, Basal ganglia disease, biotin-responsive, Acidemia, isovaleric, Acrodermatitis enteropathica, Adenine phosphoribosyltransferase deficiency, Adrenal hyperplasia, congenital, type 5, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Hyperinsulinemic hypoglycemia, familial, 6, HHH syndrome, Glycogen Storage Disease IB, Hyperphenylalaninemia, BH4-Deficient, B, Thyroid Dyshormonogenesis 3, Thyroid Dyshormonogenesis 5, Glycogen Storage Disease IC, Carnitine-Acylcarnitine Translocase Deficiency, Glycogen Storage Disease IXB, Thyroid Dyshormonogenesis 2A, Intrinsic Factor Deficiency, Hyperparathyroidism, Neonatal Severe Primary, Diabetes Mellitus, Permanent Neonatal, With Neurologic Features, Diabetes Mellitus, Permanent Neonatal, Maturity-Onset Diabetes of the Young, Type 4, Thyroid Dyshormonogenesis 6, Thyroid Dyshormonogenesis 1, Tuberous Sclerosis 1, Molybdenum Cofactor Deficiency, Complementation Group A, Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency, Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type, Tuberous Sclerosis 2, Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency, Trifunctional Protein Deficiency With Myopathy And Neuropathy, Arginine-Glycine Amidinotransferase Deficiency, Jervell And Lange-Nielsen Syndrome 2, Glycogen Storage Disease, Type IXA2, Pituitary Hormone Deficiency, Combined, 1, Glycogen Storage Disease IXC, Anemia, Sickle Cell, Hemophilia B, Congenital Hypothyroidism, Cystic Fibrosis, Cystinosis, Diabetes Mellitus, Disease, Epilepsy, Epilepsies, Myoclonic, Factor VII Deficiency, Factor X Deficiency, Fragile X Syndrome, Fructose Intolerance, Galactosemias, Glycogen Storage Disease Type I, Glucosephosphate Dehydrogenase Deficiency, Glycogen Storage Disease Type II, Granulomatous Disease, Chronic, Hemophilia A, Hepatolenticular Degeneration, Homocystinuria, Hypophosphatasia, Menkes Kinky Hair Syndrome, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Mucopolysaccharidosis I, Mucopolysaccharidosis III, Mucopolysaccharidosis IV, Mucopolysaccharidosis VI, Muscular Atrophy, Spinal, Nephritis, Hereditary, Phenylketonurias, Prader-Willi Syndrome, Pseudohypoaldosteronism, Retinoblastoma, Stress Disorders, Post-Traumatic, Waardenburg Syndrome, Wolman Disease, Fructose-1,6-Diphosphatase Deficiency, Rett Syndrome, Gyrate Atrophy, Mucopolysaccharidosis II, Mucopolysaccharidosis VII, beta-Thalassemia, Angelman Syndrome, Canavan Disease, Multiple Endocrine Neoplasia Type 2b, Peroxisomal Disorders, Smith-Lemli-Opitz Syndrome, Xanthomatosis, Cerebrotendinous, Citrullinemia, Hyperargininemia, Ornithine Carbamoyltransferase Deficiency Disease, Carbamoyl-Phosphate Synthase I Deficiency Disease, Tyrosinemias, Muscular Dystrophy, Duchenne, Aortic Stenosis, Supravalvular, Hermanski-Pudlak Syndrome, Biotinidase Deficiency, Holocarboxylase Synthetase Deficiency, Jervell-Lange Nielsen Syndrome, Mineralocorticoid Excess Syndrome, Apparent, Congenital Hyperinsulinism, Niemann-Pick Disease, Type A, Niemann-Pick Disease, Type C, Familial Hypophosphatemic Rickets, X-Linked Combined Immunodeficiency Diseases, Propionic Acidemia, von Willebrand Disease, Type 3, Argininosuccinic Aciduria, Barth Syndrome, Liddle Syndrome

Corticobasal Degeneration, Alzheimer Disease, Amyotrophic Lateral Sclerosis, Uterine Cervical Neoplasms, Dementia, Diabetes Mellitus, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Huntington Disease, Macular Degeneration, Multiple Sclerosis, Neuronal Ceroid-Lipofuscinoses, Ovarian Neoplasms, Parkinson Disease, Stress Disorders, Post-Traumatic, Supranuclear Palsy, Progressive, Uterine Neoplasms, Vaginal Neoplasms, Vulvar Neoplasms, Multiple System Atrophy, Parkinsonian Disorders, Lewy Body Disease, Frontotemporal Dementia

Amyotrophic Lateral Sclerosis, Anxiety Disorders, Arthritis, Rheumatoid, Asthma, Atrial Fibrillation, Brain Neoplasms, Breast Neoplasms, Cerebral Palsy, Cluster Headache, Colitis, Ulcerative, Colonic Neoplasms, Crohn Disease, Deafness, Depression, Diabetes Mellitus, Eczema, Epilepsy, Fibromyalgia, Heart Failure, Hypertension, Hyperthyroidism, Hypothyroidism, Infertility, Leiomyoma, Lung Neoplasms, Lyme Disease, Lymphoma, Macular Degeneration, Migraine Disorders, Multiple Sclerosis, Neoplasms, Osteoarthritis, Osteoporosis, Ovarian Cysts, Ovarian Neoplasms, Parkinson Disease, Phantom Limb, Prostatic Neoplasms, Psoriasis, Skin Neoplasms, Spinal Cord Injuries, Spinal Stenosis, Stress Disorders, Post-Traumatic, Thyroid Neoplasms, Tinnitus, Fatigue Syndrome, Chronic, Tension-Type Headache, Stroke, Pulmonary Disease, Chronic Obstructive, Irritable Bowel Syndrome, Renal Insufficiency, Chronic, Angina, Stable

Chronic Disease, Pain, Stress Disorders, Post-Traumatic, Chronic Pain

Anxiety Disorders, Depression, Myasthenia Gravis, Stress Disorders, Post-Traumatic

Autism Spectrum Disorder, Acquired Immunodeficiency Syndrome, Anemia, Sickle Cell, Epilepsy, Glaucoma, Huntington Disease, Multiple Sclerosis, Muscle Spasticity, Neoplasms, Pain, Intractable, Parkinson Disease, Stress Disorders, Post-Traumatic, Inflammatory Bowel Diseases, Dyskinesias

Neurofibromatosis 1, Stress Disorders, Post-Traumatic

Breast Neoplasms, Cognition Disorders, Stress Disorders, Post-Traumatic

Lymphoma, Stress Disorders, Post-Traumatic

Depression, Stress Disorders, Post-Traumatic