Daniel J Costello
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Explore the profile of Daniel J Costello including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Larkin J, Munteanu T, Dolan E, Costello D, Sweeney K, Kilbride R, et al.
Epilepsy Behav Rep
. 2025 Feb;
29:100747.
PMID: 39995638
The insula can generate seizures which mimic frontal, temporal and parietal epilepsies making electroclinical localization difficult. We report the case of a twenty-one-year-old woman who presented with seizure semiology of...
2.
Dudley A, Costello D
Epilepsy Behav
. 2025 Jan;
164:110250.
PMID: 39826179
Objective: Multifocal epilepsy is an important subtype of epilepsy, but it is sometimes difficult to recognise in general clinical practice. Distinguishing (uni)focal from multifocal drug resistant epilepsy is important when...
3.
Wiens K, Miller M, Costello D, Solomon A, Hilbert S, Shipper A, et al.
medRxiv
. 2024 Dec;
PMID: 39711701
Background: Monitoring and treating diarrheal illness often rely on individuals seeking care at hospitals or clinics. Cases that seek care through pharmacies and community health workers (CHW) are frequently excluded...
4.
Vasey M, Tai X, Thorpe J, Jones G, Ashby S, Hallab A, et al.
Epilepsia Open
. 2024 Sep;
9(5):1931-1947.
PMID: 39225433
Objective: To characterize the experience of people with epilepsy and aligned healthcare workers (HCWs) during the first 18 months of the COVID-19 pandemic and compare experiences in high-income countries (HICs)...
5.
Visuttijai K, Hedberg-Oldfors C, Costello D, Bermingham N, Oldfors A
Neuropathol Appl Neurobiol
. 2024 Jun;
50(3):e12995.
PMID: 38923610
Aims: Polyglucosan storage disorders represent an emerging field within neurodegenerative and neuromuscular conditions, including Lafora disease (EPM2A, EPM2B), adult polyglucosan body disease (APBD, GBE1), polyglucosan body myopathies associated with RBCK1...
6.
Fullam S, Costello D
Epilepsy Behav
. 2024 Apr;
155:109783.
PMID: 38642527
Objectives: This incidence of non-epileptic seizures (NES) is estimated at 1-35 per 100,000 population. While many patients achieve remission, a significant fraction of patients have a poor prognosis despite optimal...
7.
Costello D, Matthews E, Aurangzeb S, Doran E, Stack J, Wesselingh R, et al.
Epilepsia
. 2024 Mar;
65(6):1581-1588.
PMID: 38498313
Objective: New-onset refractory status epilepticus (NORSE) is a rare but severe clinical syndrome. Despite rigorous evaluation, the underlying cause is unknown in 30%-50% of patients and treatment strategies are largely...
8.
Pena-Ceballos J, Moloney P, Valentin A, ODonnell C, Colleran N, Liggan B, et al.
Seizure
. 2023 Oct;
112:98-105.
PMID: 37778300
Objective: Refractory idiopathic generalised epilepsy (IGE; also known as genetic generalised epilepsy) is a clinical challenge due to limited available therapeutic options. While vagus nerve stimulation (VNS) is approved as...
9.
Moloney P, Kearney H, Benson K, Costello D, Cavalleri G, Gorman K, et al.
Eur J Neurol
. 2023 Jul;
30(10):3341-3346.
PMID: 37422919
Background: Pathogenic variants in the GAP activity towards RAGs 1 (GATOR1) complex genes (DEPDC5, NPRL2, NPRL3) cause focal epilepsy through hyperactivation of the mechanistic target of rapamycin pathway. We report...
10.
Bhatia M, Cavalleri G, White M, Delanty N, Sweeney B, Costello D, et al.
Cold Spring Harb Mol Case Stud
. 2022 Nov;
8(7).
PMID: 36396431
Haploinsufficiency of the methyl-CpG-binding domain protein 5 () gene causes a neurodevelopmental disorder that includes intellectual disability, developmental delay, speech impairment, seizures, sleep disturbances, and behavioral difficulties. Microdeletion of 2q23.1...