Gisele Ishak, M.D.

Co-Division Chief of Fetal Imaging
Associate Professor

Pediatric Radiology

Biography

Dr. Ishak is an assistant professor of pediatric radiology at Seattle Children’s.

Recent Publications (via Semantic Scholar)

Changes to pediatric brain tumors in 2021 World Health Organization classification of tumors of the central nervous system.
M. Oztek, Sakura Noda, Erin K Romberg, et al. - Published 2022 - PEDIATRIC RADIOLOGY

SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
V. Serpieri, F. D’Abrusco, J. Dempsey, et al. - Published 2021 - JOURNAL OF MEDICAL GENETICS

Imaging of Horner syndrome in pediatrics: association with neuroblastoma
Hedieh Khalatbari, G. Ishak - Published 2020 - PEDIATRIC RADIOLOGY

Deep medullary vein engorgement and superficial medullary vein engorgement: two patterns of perinatal venous stroke
Hedieh Khalatbari, Jason N Wright, G. Ishak, et al. - Published 2020 - PEDIATRIC RADIOLOGY

Reply
J.N. Wright, D.W.W. Shaw, G. Ishak, et al. - Published 2020 - AMERICAN JOURNAL OF NEURORADIOLOGY

Cerebellar Watershed Injury in Children
J.N. Wright, D.W.W. Shaw, G. Ishak, et al. - Published 2020 - AMERICAN JOURNAL OF NEURORADIOLOGY

Correction to: Subdural hemorrhage rebleeding in abused children: frequency, associations and clinical presentation
Jason N Wright, T. Feyma, G. Ishak, et al. - Published 2020 - PEDIATRIC RADIOLOGY

Glial injury in neurotoxicity after pediatric CD19‐directed chimeric antigen receptor T cell therapy
J. Gust, Olivia C. Finney, Daniel H Li, et al. - Published 2019 - ANNALS OF NEUROLOGY

Subdural hemorrhage rebleeding in abused children: frequency, associations and clinical presentation
Jason N Wright, T. Feyma, G. Ishak, et al. - Published 2019 - PEDIATRIC RADIOLOGY

Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome
J. N. Dines, Yajuan J. Liu, W. Neufeld-Kaiser, et al. - Published 2019 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A