[Guideline for the diagnosis and treatment of common neonatal diseases in primary healthcare institutions: neonatal seizures (2025)]. [PDF]
Subspecialty Group of Neonatology +4 more
europepmc +1 more source
[Efficacy and safety of perampanel add-on therapy in children with epilepsy of genetic etiology]. [PDF]
Yi JQ, Sun D.
europepmc +1 more source
[Two cases of Coffin-Siris syndrome type 3 caused by de novoSMARCB1 gene mutations]. [PDF]
Jin Y, Li MQ, Yang YL.
europepmc +1 more source
[Case Report of One Family With Coffin-Lowry Syndrome and Literature Review of 28 Cases in China]. [PDF]
Zhu D, Yang W, Zhang L.
europepmc +1 more source
[Wavelet entropy analysis for ictal electroencephalogram signals of child absence epilepsy]. [PDF]
Zhang M +6 more
europepmc +1 more source
[Two cases of creatine deficiency syndrome caused by GAMT gene mutations and literature review]. [PDF]
Zhao TT +6 more
europepmc +1 more source
[Sampling intervals dependent feature extraction for state transfer networks of epileptic signals]. [PDF]
Zhang L, Yan S, Gu C.
europepmc +1 more source
[Screen exposure status and related factors in children with epilepsy]. [PDF]
Wang SJ, Li Y, Hu MZ, Zhu YH, Cui NX.
europepmc +1 more source
[Neurodevelopmental outcomes in different types of neonatal stroke]. [PDF]
Miao JW +6 more
europepmc +1 more source
[Cardiofaciocutaneous syndrome caused by microdeletion of chromosome 19p13.3: a case report and literature review]. [PDF]
Li CY +7 more
europepmc +1 more source

