Hydrocephalus

Displaying 1 - 8 of 8CSV
LaValley, M. N., Asadourian, P. A., Valenti, A. B., Hoffman, C. E., & Imahiyerobo, T. A. (2024). The Lost and Variable Cause: A Systematic Review of Shunt-Related Craniosynostosis Occurrence. Journal of Craniofacial Surgery, 35(5), 1466–1470. https://doi.org/10.1097/scs.0000000000010404
Publication Date
Stanbouly, D., Asi, A. M., Ascherman, J. A., Chuang, S.-K., Kinard, B., & Melville, J. C. (2024). Are Patients with Syndromic Craniosynostosis at Greater Risk for Epilepsy than Patients with Nonsyndromic Craniosynostosis? World Neurosurgery, 181, e45–e54. https://doi.org/10.1016/j.wneu.2023.06.024
Publication Date
Mustafa, H. J., Sambatur, E. V., Barbera, J. P., Pagani, G., Yaron, Y., Baptiste, C. D., Wapner, R. J., & Khalil, A. (2023). Diagnostic yield with exome sequencing in prenatal severe bilateral ventriculomegaly: a systematic review and meta-analysis. American Journal of Obstetrics & Gynecology MFM, 5(9), 101048. https://doi.org/10.1016/j.ajogmf.2023.101048
Publication Date
Brar, B. K., Thompson, M. G., Vora, N. L., Gilmore, K., Blakemore, K., Miller, K. A., Giordano, J., Dufke, A., Wong, B., Stover, S., Lianoglou, B., Van den Veyver, I., Dempsey, E., Rosner, M., Chong, K., Chitayat, D., Sparks, T. N., Norton, M. E., … Wapner, R. (2022). Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenatal Diagnosis, 42(13), 1686–1693. Portico. https://doi.org/10.1002/pd.6269
Publication Date
Rubinos, C., Kwon, S. B., Megjhani, M., Terilli, K., Wong, B., Cespedes, L., Ford, J., Reyes, R., Kirsch, H., Alkhachroum, A., Velazquez, A., Roh, D., Agarwal, S., Claassen, J., Connolly, E. S., & Park, S. (2022). Predicting Shunt Dependency from the Effect of Cerebrospinal Fluid Drainage on Ventricular Size. Neurocritical Care, 37(3), 670–677. https://doi.org/10.1007/s12028-022-01538-8
Publication Date
Stanbouly, D., Radley, B., Steinberg, B., & Ascherman, J. A. (2022). What Are the Risk Factors for Epilepsy Among Patients With Craniosynostosis? Journal of Oral and Maxillofacial Surgery, 80(7), 1191–1197. https://doi.org/10.1016/j.joms.2022.02.005
Publication Date
Barua, S., Berger, S., Pereira, E. M., & Jobanputra, V. (2022). Expanding the phenotype of ATP6AP1 deficiency. Molecular Case Studies, 8(4), a006195. https://doi.org/10.1101/mcs.a006195
Publication Date