Giant, symptomatic mixed vascular malformation containing a cavernoma, developmental venous anomaly, and capillary telangiectasia in a 19-month-old infant.

MLA

Gaztanaga, Wendy, et al. “Giant, Symptomatic Mixed Vascular Malformation Containing a Cavernoma, Developmental Venous Anomaly, and Capillary Telangiectasia in a 19-Month-Old Infant.” Child’s Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery, vol. 38, no. 5, May 2022, pp. 1005–09. EBSCOhost, https://doi.org/10.1007/s00381-021-05358-7.

APA

Gaztanaga, W., Luther, E., McCarthy, D., Chamyan, G., Wang, S., & Ragheb, J. (2022). Giant, symptomatic mixed vascular malformation containing a cavernoma, developmental venous anomaly, and capillary telangiectasia in a 19-month-old infant. Child’s Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery, 38(5), 1005–1009. https://doi.org/10.1007/s00381-021-05358-7

Chicago

Gaztanaga, Wendy, Evan Luther, David McCarthy, Gabriel Chamyan, Shelly Wang, and John Ragheb. 2022. “Giant, Symptomatic Mixed Vascular Malformation Containing a Cavernoma, Developmental Venous Anomaly, and Capillary Telangiectasia in a 19-Month-Old Infant.” Child’s Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery 38 (5): 1005–9. doi:10.1007/s00381-021-05358-7.