Clinical Trials

Asthma, Cystic Fibrosis, Lung Diseases, Pulmonary Fibrosis, Tuberous Sclerosis, Sarcoidosis, Pulmonary, alpha 1-Antitrypsin Deficiency

Hypothalamic hamartomas, Focal Cortical Dysplasia, Encephalitis, Epilepsies, Partial, Tuberous Sclerosis, Hemimegalencephaly

Lung Diseases, Pneumothorax, Tuberous Sclerosis, Lymphangioleiomyomatosis

Seizures, Tuberous Sclerosis

Tuberous Sclerosis, Angiomyolipoma

Focal Cortical Dysplasia, Tuberous Sclerosis

Neoplastic Syndromes, Hereditary, Tuberous Sclerosis

Mental Disorders, Tuberous Sclerosis

Epilepsies, Myoclonic, Liver Cirrhosis, Tuberous Sclerosis, Lennox Gastaut Syndrome

Behavior, Seizures, Tuberous Sclerosis

Epilepsies, Myoclonic, Seizures, Tuberous Sclerosis, Lennox Gastaut Syndrome

Tuberous Sclerosis

Turcot syndrome, Juvenile polyposis syndrome, Choroid Plexus Carcinoma, GATA2 Deficiency, Basal Cell Nevus Syndrome, Colorectal Neoplasms, Hereditary Nonpolyposis, Fanconi Anemia, Hamartoma Syndrome, Multiple, von Hippel-Lindau Disease, Hodgkin Disease, Lymphoma, Non-Hodgkin, Melanoma, Neuroblastoma, Neurofibromatosis 1, Noonan Syndrome, Pancreatic Neoplasms, Paraganglioma, Peutz-Jeghers Syndrome, Pheochromocytoma, Rothmund-Thomson Syndrome, Adenomatous Polyposis Coli, Retinoblastoma, Rhabdomyosarcoma, Tuberous Sclerosis, Neurofibromatosis 2, Li-Fraumeni Syndrome, Adrenocortical Carcinoma, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Dyskeratosis Congenita, Genetic Predisposition to Disease, Anemia, Diamond-Blackfan, Carney Complex, Hereditary Breast and Ovarian Cancer Syndrome

Carcinoma, Renal Cell, Carcinoma, Hepatocellular, Tuberous Sclerosis, Neuroendocrine Tumors

Creatine deficiency, X-linked, Telomeric 22q13 Monosomy Syndrome, Chromosome 15q, partial deletion, Fragile X Syndrome, Hamartoma Syndrome, Multiple, Tuberous Sclerosis, Rett Syndrome, Angelman Syndrome

Tuberous Sclerosis, Lymphangioleiomyomatosis

Epilepsy, Tuberous Sclerosis

Tuberous Sclerosis, Lymphangioleiomyomatosis

von Hippel-Lindau Disease, Neurofibromatosis 1, Sturge-Weber Syndrome, Tuberous Sclerosis, Neurocutaneous Syndromes

Drug Resistant Epilepsy, Epilepsy, Tuberous Sclerosis

Focal Cortical Dysplasia, Tuberous Sclerosis, Hemimegalencephaly

CDKL5 deficiency disorder, Epilepsy, Epilepsies, Myoclonic, Tuberous Sclerosis, Lennox Gastaut Syndrome

Erythema, Exanthema, Fibroma, Tuberous Sclerosis, Facies

Focal Cortical Dysplasia, Tuberous Sclerosis

Focal Cortical Dysplasia, Tuberous Sclerosis

Tuberous Sclerosis 1, Tuberous Sclerosis 2, Epilepsy, Epilepsies, Myoclonic, Seizures, Spasms, Infantile, Tuberous Sclerosis, Lennox Gastaut Syndrome

Tuberous Sclerosis

Tuberous Sclerosis

Epileptic Encephalopathy, Early Infantile, 4, Movement Disorders, Tuberous Sclerosis

Telomeric 22q13 Monosomy Syndrome, Developmental Disabilities, DiGeorge Syndrome, Down Syndrome, Fragile X Syndrome, Klinefelter Syndrome, Prader-Willi Syndrome, Tuberous Sclerosis, Turner Syndrome, Rett Syndrome, Angelman Syndrome, Williams Syndrome, Muscular Dystrophy, Duchenne, Smith-Magenis Syndrome

Autism Spectrum Disorder, Anxiety Disorders, Attention Deficit Disorder with Hyperactivity, Autistic Disorder, DiGeorge Syndrome, Fragile X Syndrome, Tourette Syndrome, Tic Disorders, Tuberous Sclerosis, 22q11 Deletion Syndrome, Neurodevelopmental Disorders

Tuberous Sclerosis

Tuberous Sclerosis, Lymphangioleiomyomatosis

Seizures, Tuberous Sclerosis

Albinism, Basal Cell Nevus Syndrome, Cutis Laxa, Ectodermal Dysplasia, Epidermolysis Bullosa, Ichthyosis, Keratoderma, Palmoplantar, Tuberous Sclerosis, Xeroderma Pigmentosum, Birt-Hogg-Dube Syndrome

Albinism, Basal Cell Nevus Syndrome, Cutis Laxa, Ectodermal Dysplasia, Epidermolysis Bullosa, Ichthyosis, Keratoderma, Palmoplantar, Tuberous Sclerosis, Birt-Hogg-Dube Syndrome

Tuberous Sclerosis

CDKL5 deficiency disorder, Epilepsy, Epilepsies, Myoclonic, Tuberous Sclerosis, Lennox Gastaut Syndrome

Epilepsy, Tuberous Sclerosis

Epilepsy, Tuberous Sclerosis

Kidney Diseases, Tuberous Sclerosis

Epilepsy, Tuberous Sclerosis

Tuberous Sclerosis

CDKL5 deficiency disorder, Epilepsy, Epilepsies, Myoclonic, Tuberous Sclerosis, Lennox Gastaut Syndrome

Nephronophthisis, familial juvenile, Treatment Adherence and Compliance, Albuminuria, Diabetes Mellitus, Hypertension, Polycystic Kidney Diseases, Tuberous Sclerosis, Renal Insufficiency, Chronic, Kidney Diseases, Cystic

Tuberous Sclerosis

Autistic Disorder, Intellectual Disability, Tuberous Sclerosis

Tuberous Sclerosis

Carney-Stratakis Syndrome, Carney Triad, Pituitary Adenoma, Familial Isolated, Colorectal Neoplasms, Hereditary Nonpolyposis, Hamartoma Syndrome, Multiple, von Hippel-Lindau Disease, Adenoma, Islet Cell, Neurofibromatosis 1, Paraganglioma, Pheochromocytoma, Pituitary Neoplasms, Tuberous Sclerosis, Li-Fraumeni Syndrome, Carcinoma, Medullary, Neuroendocrine Tumors, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Gastrointestinal Stromal Tumors, Hyperparathyroidism, Primary, Carney Complex

Epilepsy, Tuberous Sclerosis