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Journal of Neurosurgery. Pediatrics|July 4, 2012
Image-guided cerebrospinal fluid shunting in children: catheter accuracy and shunt survivalMichael R Levitt, Brent R O'Neill, Gisele E Ishak, et al.
AJNR. American Journal of Neuroradiology|April 14, 2012
Tract-based spatial statistical analysis of diffusion tensor imaging in pediatric patients with mitochondrial disease: widespread reduction in fractional anisotropy of white matter tractsG E Ishak, A V Poliakov, S L Poliachik, et al.
Pediatric Radiology|May 24, 2020
Correction to: Subdural hemorrhage rebleeding in abused children: frequency, associations and clinical presentationJason N Wright, Timothy J Feyma, Gisele E Ishak, et al.
Pediatric Radiology|November 21, 2019
Subdural hemorrhage rebleeding in abused children: frequency, associations and clinical presentationJason N Wright, Timothy J Feyma, Gisele E Ishak, et al.
Developmental Medicine and Child Neurology|June 20, 2014
Callosal alterations in pyridoxine-dependent epilepsySeth D Friedman, Gisele E Ishak, Sandra L Poliachik, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 10, 2013
Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Human Mutation|June 23, 2015
KIAA0586 is Mutated in Joubert SyndromeRuxandra Bachmann-Gagescu, Ian G Phelps, Jennifer C Dempsey, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 3, 2013
Diffusion tensor imaging of the superior cerebellar peduncle identifies patients with posterior fossa syndromeJeffrey G Ojemann, Savannah C Partridge, Andrew V Poliakov, et al.
Brain : a Journal of Neurology|March 28, 2012
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severityGisele E Ishak, Jennifer C Dempsey, Dennis W W Shaw, et al.
American Journal of Medical Genetics. Part A|July 12, 2019
Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndromeJennifer N Dines, Yajuan J Liu, Whitney Neufeld-Kaiser, et al.
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