S.C. Neurologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
NGS-Based Genetic Approach to Identify Rare Lysosomal Storage Disorders in Patients With Neurological Manifestations	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, lysosomal storage disease, metabolic disease	Active, not recruiting	Not applicable	2026-10-07		NCT07863479

Clinical trials