The European STXBP1 Consortium
ESCO is an investigator-driven consortium focused on STXBP1 research.
The European STXBP1 Consortium Instagram
The European STXBP1 Consortium Instagram
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Homepage - ESCO
Homepage - ESCO
About The European STXBP1 Consortium ESCO is an investigator-driven consortium of currently 7 European countries and Israel focused on promoting […]
Move to Cure Europe - ESCO STXBP1 Awareness Month Relay
Move to Cure Europe - ESCO STXBP1 Awareness Month Relay
Move to Cure Europe – STXBP1 Awareness Month 2025 Support the relay. Support the research. One Europe. One cause. This […]
Doneer aan Estafetterun STXBP1 (Netherlands)
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Doneer aan Estafetterun STXBP1 (Netherlands)
European STXBP1 Summit 2025
European STXBP1 Summit 2025
Capsida Receives FDA IND Clearance for Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy - Capsida Biotherapeutics
Capsida Receives FDA IND Clearance for Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy - Capsida Biotherapeutics
CAP-002 is the first engineered IV-delivered gene therapy that crosses the blood-brain-barrier and detargets the liver and dorsal root ganglia to enter the clinic THOUSAND OAKS, Calif., May 12, 2025 — Capsida Biotherapeutics (“Capsida”) today announced the U.S. Food and Drug Administration (FDA) has cleared the Investigational New Drug (IND) application for CAP-002, its wholly
‘You constantly have to be switched on’: A qualitative interview study of parents of children with STXBP1-related disorders in the Netherlands - Orphanet Journal of Rare Diseases
‘You constantly have to be switched on’: A qualitative interview study of parents of children with STXBP1-related disorders in the Netherlands - Orphanet Journal of Rare Diseases
Disorder-related variants in the STXBP1 gene are increasingly detected in children with severe developmental disorders. It is commonly acknowledged that de
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STXBP1 Foundation
STXBP1 Foundation
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