Bryan J. Lynch
Children's Health Ireland at Crumlin(IE)
Publications by Year
Research Areas
Epilepsy research and treatment, Mitochondrial Function and Pathology, Ion Transport and Channel Regulation, Escherichia coli research studies, Complement system in diseases
Most-Cited Works
- → De novo mutations in ATP1A3 cause alternating hemiplegia of childhood(2012)418 cited
- → Neurologic Complications of Pediatric Heart Transplantation(1994)67 cited
- → Natural history and outcome of neonatal hypocalcemic and hypomagnesemic seizures(1994)47 cited
- → Neurological involvement in children with hemolytic uremic syndrome(2021)35 cited
- → RHOBTB2 Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of Childhood(2021)29 cited
- → Pseudoexon activation increases phenotype severity in a Becker muscular dystrophy patient(2015)26 cited
- → Everolimus precision therapy for the GATOR1‐related epilepsies: A case series(2023)26 cited
- → Partial status epilepticus – Rapid genetic diagnosis of Alpers’ disease(2011)13 cited
- → Correlation of99mTc-HMPAO SPECT with EEG monitoring: prognostic value for outcome of epilepsy surgery in children(1995)10 cited
- → Status dystonicus due to missense variant in ARX: Diagnosis and management(2018)8 cited