none58noBackground and Objectives Clinical manifestations in STXBP1 developmental and epileptic encephalopathy (DEE) vary in severity and outcome, and the genotypic spectrum is diverse. We aim to trace the neurodevelopmental trajectories in individuals with STXBP1-DEE and dissect the relationship between neurodevelopment and epilepsy. Methods Retrospective standardized clinical data were collected through international collaboration. A composite neurodevelopmental score system compared the developmental trajectories in STXBP1-DEE. Results Forty-eight patients with de novo STXBP1 variants and a history of epilepsy were included (age range at the time of the study: 10 months to 35 years, mean 8.5 years). At the time of inclusion,65...
OBJECTIVE: The aim of this study was to expand the spectrum of epilepsy syndromes related to STX1B, ...
Abstract: Background: De novo loss of function mutations in STXBP1 are a relatively common cause of ...
BACKGROUND:De novo loss of function mutations in STXBP1 are a relatively common cause of epilepsy an...
Background and Objectives Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and Objectives Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and ObjectivesClinical manifestations in STXBP1 developmental and epileptic encephalopath...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
OBJECTIVE To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encep...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
OBJECTIVE: The aim of this study was to expand the spectrum of epilepsy syndromes related to STX1B, ...
Abstract: Background: De novo loss of function mutations in STXBP1 are a relatively common cause of ...
BACKGROUND:De novo loss of function mutations in STXBP1 are a relatively common cause of epilepsy an...
Background and Objectives Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and Objectives Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and ObjectivesClinical manifestations in STXBP1 developmental and epileptic encephalopath...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
Background and objectives: Clinical manifestations in STXBP1 developmental and epileptic encephalopa...
OBJECTIVE To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encep...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
Objective: To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encepha...
OBJECTIVE: The aim of this study was to expand the spectrum of epilepsy syndromes related to STX1B, ...
Abstract: Background: De novo loss of function mutations in STXBP1 are a relatively common cause of ...
BACKGROUND:De novo loss of function mutations in STXBP1 are a relatively common cause of epilepsy an...