Akbari, SH A; Rizvi, AA; CreveCoeur, TS; Han, RH; Greenberg, JK; Torner, J; Brockmeyer, DL; Wellons, JC; Leonard, JR; Mangano, FT; et al. Socioeconomic and demographic factors in the diagnosis and treatment of Chiari malformation type I and syringomyelia. Journal of Neurosurgery: Pediatrics. 2022; 1-10.

Akbari, SH A; Yahanda, AT; Ackerman, LL; Adelson, PD; Ahmed, R; Albert, GW; Aldana, PR; Alden, TD; Anderson, RC E; Bauer, DF; et al. Complications and outcomes of posterior fossa decompression with duraplasty versus without duraplasty for pediatric patients with Chiari malformation type I and syringomyelia: a study from the Park-Reeves Syringomyelia Research Consortium. Journal of Neurosurgery: Pediatrics. 2022; 1-13.

Arya, R; Ervin, B; Buroker, J; Greiner, HM; Byars, AW; Rozhkov, L; Skoch, J; Horn, PS; Frink, C; Scholle, C; et al. Neuronal Circuits Supporting Development of Visual Naming Revealed by Intracranial Coherence Modulations. Frontiers in Neuroscience. 2022; 16.

Arya, S; Kingma, ML; Dornette, S; Weber, A; Bardua, C; Mierke, S; Kingma, PS. Comparison of Airway Pressure Release Ventilation to High-Frequency Oscillatory Ventilation in Neonates with Refractory Respiratory Failure. International Journal of Pediatrics. 2022; 2022.

DeWire, M; Lazow, M; Campagne, O; Leach, J; Fuller, C; Senthil Kumar, S; Stanek, J; de Blank, P; Hummel, TR; Pillay-Smiley, N; et al. Phase I study of ribociclib and everolimus in children with newly diagnosed DIPG and high-grade glioma: A CONNECT pediatric neuro-oncology consortium report. Neuro-Oncology Advances. 2022; 4.

Duy, PQ; Weise, SC; Marini, C; Li, XJ; Liang, D; Dahl, PJ; Ma, S; Spajic, A; Dong, W; Juusola, J; et al. Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus. Nature Neuroscience. 2022; 25:458-473.

Forde, B; Lim, F; Peiro, J; Stevenson, C; Tabbah, S; Habli, M. A case series of subsequent pregnancy outcomes after fetoscopic MMC repair. American Journal of Obstetrics and Gynecology. 2022; 226:s492-s493.

Harpster, K; Weckherlin, N; Engsberg, JR; Powell, SK; Barnard, H; Kadis, D; Dodd, JN; Garrett, ML; Mangano, FT; Limbrick, DD; et al. An iPad-based intervention to improve visual-motor, visual-attention, and visual-perceptual skills in children with surgically treated hydrocephalus: A pilot study. Child's Nervous System. 2022; 38:303-310.

Iwasawa, E; Brown, FN; Shula, C; Kahn, F; Lee, SH; Berta, T; Ladle, DR; Campbell, K; Mangano, FT; Goto, J. The Anti-Inflammatory Agent Bindarit Attenuates the Impairment of Neural Development through Suppression of Microglial Activation in a Neonatal Hydrocephalus Mouse Model. Journal of Neuroscience. 2022; 42:1820-1844.

McMahon, R; Morgan, SJ; Brooks, JT; Cahill, P; Fitzgerald, R; Li, Y; Pediatric Spine Study Group, ; Truong, WH. Does the presence of programmable implanted devices in patients with early onset scoliosis alter typical operative and postoperative practices? A survey of spine surgeons. Spine Deformity. 2022.

Mishreky, A; Parent, S; Miyanji, F; Smit, K; Murphy, J; Bowker, R; Al Khatib, N; El-Hawary, R; Abdullah, AS A; Ahn, E; et al. Body mass index affects outcomes after vertebral body tethering surgery. Spine Deformity. 2022; 10:563-571.

Nagaraj, UD; Venkatesan, C; Bierbrauer, KS; Kline-Fath, BM. Value of pre- and postnatal magnetic resonance imaging in the evaluation of congenital central nervous system anomalies. Pediatric Radiology. 2022; 52:802-816.

Poisson, KE; Zygmunt, A; Leino, D; Fuller, CE; Jones, BV; Haslam, D; Staat, MA; Clay, G; Ting, TV; Wesselkamper, K; et al. Lethal Pediatric Cerebral Vasculitis Triggered by Severe Acute Respiratory Syndrome Coronavirus 2. Pediatric Neurology. 2022; 127:1-5.

Roth, J; Perekopaiko, Y; Kozyrev, DA; Constantini, S; Myers, HE; Chern, BL; Reisner, A; Mena-Bernal, JH; Bartoli, A; Paun, L; et al. Pediatric colloid cysts: a multinational, multicenter study. An IFNE-ISPN-ESPN collaboration. Journal of Neurosurgery: Pediatrics. 2022; 1-8.

Weaver, KN; Care, M; Wakefield, E; Zarate, YA; Skoch, J; Gripp, KW; Prada, CE. Craniosynostosis is a feature of Costello syndrome. American Journal of Medical Genetics, Part A. 2022; 188:1280-1286.