Prodromal Parkinsonian Features in GBA1 Mutation Carriers
Prodromal Parkinsonian Features in GBA1 Mutation Carriers
Recruiting · NCT05253560 · Registry updated 2026-04-29Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Prodromal Parkinsonian Features in GBA1 Mutation Carriers | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Gaucher Disease, Type 1, Gaucher disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis | Recruiting | Not stated | 2026-04-29 | NCT05253560 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Shaare Zedek Medical Center | 21 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Michal Becker- Cohen | Jerusalem | Israel | 1 |