Example: Heart Attack
Clinical Trials on Malformations of Cortical Development
Total 91 results
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NCT02451696CompletedConditions: Epilepsy; Tuberous Sclerosis Complex; Focal Cortical Dysplasia
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NCT00687024CompletedConditions: Focal Cortical Dysplasia; Epilepsy
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NCT03198949Unknown statusConditions: Epilepsy and Focal Cortical Dysplasia II
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NCT02261753TerminatedConditions: Cortical Dysplasia
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NCT02890641RecruitingConditions: Cortical Dysplasia-Focal Epilepsy Syndrome
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NCT00041600RecruitingConditions: Epilepsy; Seizures; Cognition Disorders; Neuronal Migration Disorders
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NCT04344626RecruitingConditions: Epilepsy; Focal Cortical Dysplasia; Tuberous Sclerosis; Hemimegalencephaly; Polymicrogyria; Rasmussen Encephalitis; Sturge-Weber Syndrome; Gliosis; Stroke; Tumor, Brain
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NCT02654340RecruitingConditions: Hypomelanotic Macules; Facial Angiofibroma; Shagreen Patches; Ungual Fibromas; Cortical Dysplasia; Cardiac Rhabdomyoma; Lymphangioleiomyomatosis; Renal Angiomyolipoma; Subependymal Giant Cell Astrocytoma
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NCT00552045CompletedConditions: Epilepsy; Localization-related Epilepsy; Infantile Spasms; Lennox-Gastaut Syndrome; Polymicrogyria; Periventricular Heterotopias
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NCT03321240RecruitingConditions: Refractory Epilepsy; Focal Epilepsy; Focal Cortical Dysplasia
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NCT00686530WithdrawnConditions: Brain Malformation
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NCT04816175RecruitingConditions: Microcephaly; Hyperkinesis With Developmental Delay; Global Developmental Delay
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NCT03255369Unknown statusConditions: ZIKA VIRUS INFECTION; Child Development; Microcephaly
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NCT03548779Enrolling by invitationConditions: Epilepsy; Seizure; Neuromuscular Diseases; Brain Malformation; Intellectual Disability; Autism Spectrum Disorder; Hypotonia; Inborn Errors of Metabolism; Movement Disorders; Genetic Disease; Development Delay; Chromosome Abnormality; Hearing Loss; Dysmorphic Features; Skeletal Dysplasia; Congenital Abnormality; Microcephaly; Macrocephaly
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NCT00001639CompletedConditions: Abnormalities; Failure to Thrive; Mental Retardation; Microcephaly
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NCT04463316RecruitingConditions: Prader-Willi Syndrome; PWS-like Syndrome; Silver Russel Syndrome; Congenital Hypopituitarism; Klinefelter (XXY-)Syndrome; Congenital Adrenal Hyperplasia; XXXXY Syndrome; XXYY Syndrome; XXXX Syndrome (Tetra-X Syndrome); Disorders of Sex Development; Turner Syndrome; 46, XY DSD; Tuberous Sclerosis; Neurofibromatosis; Albright Hereditaire Osteodystrofie; Cornelia de Lange Syndrome; Saethre-Chotzen Syndrome; 17p- Deletiesyndrome; VCF Syndrome; POLR3A Mutatie; Ohdo Syndrome; Jacobsen Syndrome / 11 q Syndrome; Myrhe Syndrome; CHARGE Syndrome; 1q25-32 Deletie; Bardet Biedl Syndrome; Rett Syndrome; 22q11 Deletion Syndrome; Allan-Herndon-Dudley Syndrome; Kallmann Syndrome; Rare Bone Disorders; Noonan Syndrome; Williams-Beuren Syndrome
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NCT01151462WithdrawnConditions: Hearing Loss; Mental Retardation; Microcephaly; Chorioretinitis
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NCT03922594RecruitingConditions: Microcephaly; Congenital Infection
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NCT03651687RecruitingConditions: Microcephaly
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NCT02943304Unknown statusConditions: Microcephaly; Mental Retardation
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NCT04569149RecruitingConditions: MOPDII; MOPDI; MOPDIII; Taybi Linder Syndrome; Meier-Gorlin Syndrome; Saul-Wilson Syndrome; Ligase 4 Syndrome; Lowry Wood Syndrome; Microcephalic Primordial Dwarfism
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NCT04656171Not yet recruitingConditions: Fanconi Anemia
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NCT04595513RecruitingConditions: Tuberous Sclerosis Complex; Epilepsy
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NCT04485104RecruitingConditions: Seizure in Participants With Tuberous Sclerosis Complex
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NCT04285346RecruitingConditions: Tuberous Sclerosis