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Author Details
Full Name
William B Gallentine
Affiliation
Stanford University and Lucile Packard Children's Hospital
ORCID
Career Start Year
2007
Papers
55
H Index
23
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36930237
Survey of Pediatric ICU EEG Monitoring-Reassessment After a Decade.
J Clin Neurophysiol
2024
36826837
Diagnosis of TBC1D32-associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy.
Am J Med Genet A
2023
37338864
Automated Interpretation of Clinical Electroencephalograms Using Artificial Intelligence.
JAMA Neurol
2023
35243670
Delineating the epilepsy phenotype of NGLY1 deficiency.
J Inherit Metab Dis
2022
34023630
Alterations in coordinated EEG activity precede the development of seizures in comatose children.
Clin Neurophysiol
2021
34542573
Use and Safety of Immunotherapeutic Management of N-Methyl-d-Aspartate Receptor Antibody Encephalitis: A Meta-analysis.
JAMA Neurol
2021
34103402
Psychiatric Phenotypes of Pediatric Patients With Seropositive Autoimmune Encephalitis.
Hosp Pediatr
2021
32173161
Evaluation of Diagnostic Criteria for Hashimoto Encephalopathy Among Children and Adolescents.
Pediatr Neurol
2020
32015180
Subacute Neuropsychiatric Syndrome in Girls With <i>SHANK3</i> Mutations Responds to Immunomodulation.
Pediatrics
2020
32015175
Child Neurology: A young child with an undiagnosed case of dystonia responsive to l-dopa.
Neurology
2020
31953309
Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient.
Neurol Neuroimmunol Neuroinflamm
2020
32916380
Institutional Pediatric Convulsive Status Epilepticus Protocol Decreases Time to First and Second Line Anti-Seizure Medication Administration.
Seizure
2020
30609410
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
Am J Hum Genet
2019
31072785
Corrigendum to "Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature" [Seizure 55 (February) (2018) 1-3].
Seizure
2019
30548468
Immunotherapy in selected patients with Down syndrome disintegrative disorder.
Dev Med Child Neurol
2019
29291456
Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature.
Seizure
2018
29444762
Hemimegalencephaly with Bannayan-Riley-Ruvalcaba syndrome.
Epileptic Disord
2018
29622490
Autoimmune GFAP-Associated Meningoencephalomyelitis: A Report of a Pediatric Patient.
Pediatr Neurol
2018
29733464
Randomized trial of lacosamide versus fosphenytoin for nonconvulsive seizures.
Ann Neurol
2018
29157501
Evaluation and Management of Autoimmune Encephalitis: A Clinical Overview for the Practicing Child Psychiatrist.
Child Adolesc Psychiatr Clin N Am
2018
28633092
Epilepsy in neurofibromatosis type 1.
Epilepsy Behav
2017
28448686
Plasma cytokines associated with febrile status epilepticus in children: A potential biomarker for acute hippocampal injury.
Epilepsia
2017
28675556
Prospective clinical trials to investigate clinical and molecular biomarkers.
Epilepsia
2017
26825045
Strategies to Maximize Enrollment in a Prospective Study of Comatose Children in the PICU.
Pediatr Crit Care Med
2016
27794237
Cognitive functioning one month and one year following febrile status epilepticus.
Epilepsy Behav
2016
27265870
Risk factors for subsequent febrile seizures in the FEBSTAT study.
Epilepsia
2016
25458097
Development and validation of a seizure prediction model in critically ill children.
Seizure
2015
24161223
Electrographic seizures after convulsive status epilepticus in children and young adults: a retrospective multicenter study.
J Pediatr
2014
24502379
Emergency management of febrile status epilepticus: results of the FEBSTAT study.
Epilepsia
2014
23335026
Electroencephalographic monitoring in the pediatric intensive care unit.
Curr Neurol Neurosci Rep
2013
24961623
Reorganization and stability for motor and language areas using cortical stimulation: case example and review of the literature.
Brain Sci
2013
23848569
Electroencephalography monitoring in critically ill children: current practice and implications for future study design.
Epilepsia
2013
23794680
Electrographic seizures in pediatric ICU patients: cohort study of risk factors and mortality.
Neurology
2013
23545766
Pediatric ICU EEG monitoring: current resources and practice in the United States and Canada.
J Clin Neurophysiol
2013
23545763
Utility of continuous EEG in children with acute traumatic brain injury.
J Clin Neurophysiol
2013
23545759
Continuous EEG monitoring in the pediatric and neonatal intensive care units.
J Clin Neurophysiol
2013
22353984
Electroencephalography leads placed by nontechnologists using a template system produce signals equal in quality to technologist-applied, collodion disk leads.
J Clin Neurophysiol
2012
23027098
Genetic generalized epilepsies.
J Clin Neurophysiol
2012
22985722
Cerebrospinal fluid findings in children with fever-associated status epilepticus: results of the consequences of prolonged febrile seizures (FEBSTAT) study.
J Pediatr
2012
22749608
Electroencephalographic and seizure manifestations in two patients with folate receptor autoimmune antibody-mediated primary cerebral folate deficiency.
Epilepsy Behav
2012
22863189
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Am J Hum Genet
2012
21395567
Oculogyric crises secondary to lamotrigine overdosage.
Epilepsia
2011
22115008
Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodies.
Pediatr Neurol
2011
22115004
Cytokine storm of acute necrotizing encephalopathy.
Pediatr Neurol
2011
21292558
Electroencephalographic and seizure manifestations of pyridoxal 5'-phosphate-dependent epilepsy.
Epilepsy Behav
2011
21497558
Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy.
Epilepsy Behav
2011
20398883
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
2010
21104870
Pseudometabolic presentation of dystrophinopathy due to a missense mutation.
Muscle Nerve
2010
20837311
Pediatric neuro-Behçet's disease responsive to adalimumab.
Pediatr Neurol
2010
20522523
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
Brain
2010
1 - 50 of 55
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