Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations - Scheffer - 2014 - Annals of Neurology - Wiley Online Library
Ictal EEG: bilateral montage showing fronto-central fast activity... | Download Scientific Diagram
Familial focal epilepsy with variable foci: MedlinePlus Genetics
Dominant Focal EpilepsiesSarah Weckhuysen, Mary Kurian, Fabienne Picard, and Stephanie Baulac | Clinical Gate
Familial Focal Epilepsy with Variable Foci | SpringerLink
Deep feature fusion based childhood epilepsy syndrome classification from electroencephalogram - ScienceDirect
Frontiers | A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy
A splicing variation in NPRL2 causing familial focal epilepsy with variable foci: additional cases and literature review | Journal of Human Genetics
Abhishek Gohel on Twitter: "This handy classification divides epilepsy syndromes across age at onset, focal vs generalised vs focal + generalised, and epileptic encephalopathies. Amazing work! Ref: https://t.co/cCbaBGUnl4 #NeuroTwitter #Epilepsy https ...
Frontiers in Bioscience 13, 3159-3167, January 1, 2008] Genetic etiology of new forms of familial epilepsy Xuefeng Wang, Yang
Familial focal epilepsy with variable foci: MedlinePlus Genetics
ROL DE LA INTELIGENCIA ARTIFICIAL EN LA INTERPRETACIÓN DE PRUEBAS DE EPILEPSIA
DEPDC5 – this is what you need to know | Beyond the Ion Channel
Genetic Advances in Epilepsy - touchNEUROLOGY
JCI - DEPDC5 takes a second hit in familial focal epilepsy
DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family - Aberastury - 2019 - Epileptic Disorders - Wiley Online Library
Familial Partial Epilepsy with Variable Foci and mutations in DEPDC5 | Beyond the Ion Channel
Familial Focal Epilepsy with Variable Foci | SpringerLink
The clinical features of familial focal epilepsy with variable foci and NPRL3 gene variant | PLOS ONE
Familial Focal Epilepsy with Variable Foci | SpringerLink
Frontiers | Identification of two rare NPRL3 variants in two Chinese families with familial focal epilepsy with variable foci 3: NGS analysis with literature review
PDF) Mutations in DEPDC5 cause familial focal epilepsy with variable foci
John Libbey Eurotext - Epileptic Disorders - Magnetoencephalogram-assisted diagnosis of familial focal epilepsy with variable foci in a Chinese family with a novel DEPDC5 mutation
