Congenital Hydrocephalus: 11 Clinical Trials, Page 1 of 2

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PatientSpot Formerly Known as ArthritisPower

Condition(s):Rheumatoid Arthritis; Ankylosing Spondylitis; Fibromyalgia; Gout; Crohn Disease; Juvenile Idiopathic Arthritis; Lupus Erythematosus; Myositis; Osteoarthritis; Osteoporosis; Psoriasis; Psoriatic Arthritis; Scleroderma; Dermatomyositis; Inflammatory Bowel Diseases; Polymyositis; Axial Spondyloarthritis; Diffuse Idiopathic Skeletal Hyperostosis; Polymyalgia Rheumatica; Giant Cell Arteritis; Temporal Arteritis; Wegener; Relapsing Polychondritis; Undifferentiated Connective Tissue Disease; Spinal Cord Injuries; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Ataxia; Bell Palsy; Brain Tumor; Cerebral Aneurysm; Epilepsy; Guillain-Barre Syndrome; Headache; Head Injury; Hydrocephalus; Lumbar Disc Disease; Meningitis; Multiple Sclerosis; Muscular Dystrophy; Neurocutaneous Syndromes; Parkinson Disease; Stroke; Cluster Headache; Tension-Type Headache; Chronic Obstructive Pulmonary Disease; Asthma; Lung Cancer; Cystic Fibrosis; Sleep Apnea; Eczema; Alopecia; Chronic Inflammation; Unstable Angina; Heart Attack; Heart Failure; Arrythmia; Valve Heart Disease; High Blood Pressure; Congenital Heart Disease; Peripheral Arterial Disease; Diabetes; Chronic Liver Disease; ObesityLast Updated:December 13, 2023Recruiting

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Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

Condition(s):Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Including; Sickle Cell Disease; Cystic Fibrosis; Fragile X Syndrome; Proximal Spinal Muscular Atrophy; Myotonic Dystrophy; Muscular Dystrophy, Duchenne; Muscular Dystrophy, Becker; Neurofibromatosis-Noonan Syndrome; Huntington Disease; Hemophilia A; Hemophilia B; MODY2 Diabetes; X-Linked Hydrocephalus; Autosomal Recessive Polycystic Kidney DiseaseLast Updated:February 28, 2024Not yet recruiting

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