Childhood absence epilepsy and febrile seizures: a family with a GABAA receptor mutation [PDF]
Carla Marini +5 more
openalex +1 more source
Continuous outcome estimation in N‐of‐1 trials for accelerated decision‐making
Abstract Objective N‐of‐1 trials aim to determine the therapeutic effect for a single individual. This individualized approach necessitates collecting multiple data points over time through repeated alternating periods of active treatment and a comparator or control condition.
Victoria Defelippe +5 more
wiley +1 more source
Abstract Objective Dravet syndrome (DS) is the prototypic developmental and epileptic encephalopathy, characterized by drug‐resistant seizures, developmental slowing, and many other morbidities. Detailed characterization of behavioral phenotypes and social–emotional skill development are limited.
Ingrid E. Scheffer +26 more
wiley +1 more source
Differentiating Interictal and Ictal States in Childhood Absence Epilepsy through Permutation Rényi Entropy [PDF]
Nadia Mammone +3 more
openalex +1 more source
Changes of Ictal-Onset Epileptic Network Synchronicity in Childhood Absence Epilepsy: A Magnetoencephalography Study. [PDF]
Sun Y +8 more
europepmc +1 more source
Early Life Health and Adult Earnings: Evidence from a Large Sample of Siblings and Twins [PDF]
We study the relationship between early life health and adult earnings using a unique dataset that covers almost the entire population of Swedish males born between 1950 and 1970.
Lundborg, Petter +2 more
core
Abstract Despite advancements in epilepsy care, a substantial diagnostic gap persists, particularly in resource‐limited settings. This narrative review explores the potential of video‐based diagnostics augmented by artificial intelligence (AI) to address this gap by enabling earlier and more accessible seizure detection and classification.
Gadi Miron +7 more
wiley +1 more source
Constructing an Axonal-Specific Myelin Developmental Graph and its Application to Childhood Absence Epilepsy. [PDF]
Drenthen GS +7 more
europepmc +1 more source
The I–II Loop Controls Plasma Membrane Expression and Gating of Cav3.2 T-Type Ca2+Channels: A Paradigm for Childhood Absence Epilepsy Mutations [PDF]
Iuliia Vitko +5 more
openalex +1 more source
Abstract Objective Cryptogenic new onset refractory status epilepticus (cNORSE) carries high risks of long‐term disability and post‐NORSE epilepsy, but mechanisms remain unclear. We aimed to assess the predictive value of inflammatory and brain injury biomarkers and determine whether immune disturbances persist in the chronic phase. Methods We enrolled
Aurélie Hanin +34 more
wiley +1 more source

