B. Wical

发表

Rapid infusion of sodium valproate in acutely ill children.

A. Birnbaum, I. Leppik, J. Cloyd, 2003, Pediatric neurology.

Neonatal seizures and electrographic analysis: evaluation and outcomes.

B. Wical, 1994, Pediatric neurology.

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

J. Ganesh, A. Vanderver, N. Brunetti‐Pierri, 2008, Human mutation.

Dravet syndrome and parent associations: The IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief

P. Camfield, B. Wical, K. Watts, 2011, Epilepsia.

A distinctive neurologic syndrome after induced profound hypothermia.

L. Tomasi, B. Wical, Lawrence G. Tomasi, 1990, Pediatric neurology.

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

L. Lagae, P. Striano, T. Loddenkemper, 2017, Brain : a journal of neurology.

Gabapentin Successfully Manages Chronic Unexplained Irritability in Children With Severe Neurologic Impairment

L. Charnas, B. Wical, J. Hauer, 2007, Pediatrics.

Obstructive sleep apnea in children with cerebral palsy and epilepsy

B. Wical, William Wical, T. Wical, 2016, Developmental medicine and child neurology.

Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective

M. Patterson, S. Kirmani, B. Wical, 2015, Molecular Syndromology.

Components of Attention in Children with Complex Partial Seizures With and Without ADHD

M. Semrud-Clikeman, B. Wical, M. Semrud‐Clikeman, 1999, Epilepsia.

MEG evaluation of pediatric epilepsy

F. Morrell, J. Lewine, J. Shih, 1995 .

Lead: who bears the burden?

B. Wical, 1994, Archives of pediatrics & adolescent medicine.

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN 2 A-related disorders

L. Lagae, P. Striano, T. Loddenkemper, 2017 .