Author details

Full Name

Deepak Gill

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37119734	CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammation.		2023
35701389	Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice.	Developmental Medicine and Child Neurology	2023
38059324	Clinical features associated with epilepsy occurrence, resolution, and drug resistance in children with cerebral palsy: A population-based study.		2023
37340737	CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromes.	Ann Clin Transl Neurol	2023
37144751	Repeat testing enhances long-term verbal memory in children with epilepsy.		2023
34717047	Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype.	Epilepsia Open	2022
36174397	Decreased cerebrospinal fluid kynurenic acid in epileptic spasms: A biomarker of response to corticosteroids.	eBioMedicine	2022
35899185	Predictors of longitudinal seizure outcomes after epilepsy surgery in childhood.	Epilepsy and Behavior Reports	2022
35811432	Koolen-de Vries syndrome associated with continuous spike-wave in sleep	Epileptic Disorders	2022
35429468	A potential new treatment for CDKL5 deficiency disorder.	Lancet Neurology, The	2022
35617747	SPG11 presenting with dystonic tremor in childhood.	Parkinsonism and Related Disorders	2022
34920348	Status epilepticus outcomes among vaccinated and unvaccinated children: A population-based study.	Epilepsy and Behavior	2022
35259627	Accelerated long-term forgetting in children with temporal lobe epilepsy: A timescale investigation of material specificity and executive skills.	Epilepsy and Behavior	2022
33144681	NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.	Genet Med	2021
34109629	Severe speech impairment is a distinguishing feature of FOXP1-related disorder.	Developmental Medicine and Child Neurology	2021
34192493	Anterior cervical osteophytes causing dysphagia and dyspnoea.	Annals of the Royal College of Surgeons of England	2021
34082468	Integrated in silico and experimental assessment of disease relevance of PCDH19Â missense variants.	Human Mutation	2021
33142199	Accelerated long-term forgetting in children with genetic generalized epilepsy: The temporal trajectory and contribution of executive skills.	Epilepsy and Behavior	2020
32196822	Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy.	Hum Mutat	2020
31868227	BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures.	Developmental Medicine and Child Neurology	2020
33585817	Gain-of-function variants identified in vigabatrin-hypersensitive epileptic encephalopathies.	Brain Communications	2020
32882631	Deficits in all aspects of social competence identified in children who have undergone epilepsy surgery.	Epilepsy and Behavior	2020
31204815	Theory of mind and social competence in children and adolescents with temporal lobe epilepsy.	Neuropsychology	2019
31618474	The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.	Annals of Neurology	2019
31872051	Yield of comparative genomic hybridization microarray in pediatric neurology practice.	Neurology: Genetics	2019
28988644	Longitudinal study of accelerated long-term forgetting in children with genetic generalized epilepsy: Evidence of ongoing deficits.	Cortex	2019
30221764	Isolated seizures during the first episode of relapsing myelin oligodendrocyte glycoprotein antibody-associated demyelination in children.	Developmental Medicine and Child Neurology	2019
30294775	Dealing with a first seizure: accurate diagnosis and good management.	Developmental Medicine and Child Neurology	2019
29685768	Accelerated long-term forgetting and behavioural difficulties in children with epilepsy.	Cortex	2019
31283843	Etiology is the key determinant of neuroinflammation in epilepsy: Elevation of cerebrospinal fluid cytokines and chemokines in febrile infection-related epilepsy syndrome and febrile status epilepticus.	Epilepsia	2019
31133510	Facial emotion perception and social competence in children (8 to 16â¿¯years old) with genetic generalized epilepsy and temporal lobe epilepsy.	Epilepsy and Behavior	2019
30974406	A study of perfusion changes with Insula Epilepsy using SPECT.	Seizure : the journal of the British Epilepsy Association	2019
29422360	EpApp: Development and evaluation of a smartphone/tablet app for adolescents with epilepsy.	Journal of Clinical Neuroscience	2018
28956479	Psychogenic non-epileptic seizures in children and adolescents: Part II - explanations to families, treatment, and group outcomes.		2018
28956448	Psychogenic non-epileptic seizures in children and adolescents: Part I - Diagnostic formulations.		2018
29058318	Seizure outcome after corpus callosotomy in a large paediatric series.	Developmental Medicine and Child Neurology	2018
29933178	Theory of Mind and social competence in children and adolescents with genetic generalised epilepsy (GGE): Relationships to epilepsy severity and anti-epileptic drugs.	Seizure : the journal of the British Epilepsy Association	2018
30092753	Cannabidiol for treating drug-resistant epilepsy in children: the New South Wales experience.	Medical Journal of Australia	2018
29852413	Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy.	Seizure	2018
28086190	Attention deficits in children with epilepsy: Preliminary findings.	Epilepsy and Behavior	2017
28341888	The respiratory control of carbon dioxide in children and adolescents referred for treatment of psychogenic non-epileptic seizures.	European Child and Adolescent Psychiatry	2017
28794249	Not all <i>SCN1A</i> epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.	Neurology	2017
28439892	Cerebrospinal fluid cyto-/chemokine profile during acute herpes simplex virus induced anti-N-methyl-d-aspartate receptor encephalitis and in chronic neurological sequelae.	Developmental Medicine and Child Neurology	2017
27511947	Children's Experiences of Epilepsy: A Systematic Review of Qualitative Studies.	Pediatrics	2016
27237542	Corpus callosotomy outcomes in pediatric patients: AÂ systematic review.	Epilepsia	2016
26814174	Eye movement disorders are an early manifestation of CACNA1A mutations in children.	Developmental Medicine and Child Neurology	2016
26187619	Outcome of Early Juvenile Onset Metachromatic Leukodystrophy After Unrelated Cord Blood Transplantation: A Case Series and Review of the Literature.	Journal of Child Neurology	2016
26645281	Reduced complications from intracranial grid insertion by using a small grid size and a precise protocol during monitoring.	Acta Neurochir (Wien)	2016
26592968	Postencephalitic epilepsy and drug-resistant epilepsy after infectious and antibody-associated encephalitis in childhood: Clinical and etiologic risk factors.	Epilepsia	2016
27810515	Mortality in Dravet syndrome.	Epilepsy Res	2016