Showing results (1-10 of 1,026) with videos related to
Sort By:
Pageof 103
JIMD Reports|August 26, 2015
Normal Neurodevelopmental Outcomes in PNPO Deficiency: A Case Series and Literature ReviewJ Hatch, D Coman, P Clayton, et al.JIMD Reports|June 26, 2015
PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?D Coman, P Lewindon, P Clayton, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 22, 2015
A population-based post mortem study of sudden unexpected death in epilepsyDamian Clark, Kate RineyEpilepsia|July 23, 2024
Have epilepsy outcomes changed for children with tuberous sclerosis complex in Queensland, Australia?Melissa Braun, Kate RineyJIMD Reports|August 3, 2016
DMP1-CDG (CDG1e) with Significant Gastrointestinal Manifestations; Phenotype and Genotype ExpansionC Bursle, D Brown, J Cardinal, et al.Epilepsia|November 1, 2022
Clinical seizure semiology is subtle and identification of seizures by parents is unreliable in infants with tuberous sclerosis complexMatthew Lynch, Kirsty Smith, Kate RineyEuropean Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 2, 2024
Genetic causes of infection induced encephalitisOlivia-Paris Quinn, Peter McNaughton, Nolette Pereira, et al.Expert Review of Neurotherapeutics|September 7, 2023
How have the recent updated epilepsy classifications impacted on diagnosis and treatment?Elaine C Wirrell, Kate Riney, Nicola Specchio, et al.The Biochemical Journal|October 5, 2001
Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylationP Mills, K Mills, P Clayton, et al.Epilepsia Open|March 22, 2025
Epilepsy syndromes classificationElaine C Wirrell, Nicola Specchio, Rima Nabbout, et al.Pageof 103