Effective medium theory to the description of plasmonic resonances: Role of Au and Ti nanoparticles embedded in MoO(3) thin films

por Morales-Luna, Gesuri, Morales-Luna, Michael
Publicado 2020

Extinction Coefficient Modulation of MoO(3) Films Doped with Plasmonic Nanoparticles: From an Effective Medium Theory Description

por Morales-Luna, Gesuri, Morales-Luna, Michael
Publicado 2021

Personality Changes and Staring Spells in a 12-Year-Old Child: A Case Report Incorporating ChatGPT, a Natural Language Processing Tool Driven by Artificial Intelligence (AI)

por Puthenpura, Vidya, Nadkarni, Siddhi, DiLuna, Michael, Hieftje, Kimberly, Marks, Asher
Publicado 2023

A novel association of campomelic dysplasia and hydrocephalus with an unbalanced chromosomal translocation upstream of SOX9

por Antwi, Prince, Hong, Christopher S., Duran, Daniel, Jin, Sheng Chih, Dong, Weilai, DiLuna, Michael, Kahle, Kristopher T.
Publicado 2018

Biallelic inactivation of PBRM1 as a molecular driver in a rare pineoblastoma case: illustrative case

por Antonios, Joseph P., Yalcin, Kanat, Darbinyan, Armine, Koo, Andrew, Hong, Christopher S., DiLuna, Michael, Erson-Omay, Zeynep
Publicado 2022

A Review of Cerebral Shunts, Current Technologies, and Future Endeavors

por Soler, Garrett J., Bao, Mengdi, Jaiswal, Devina, Zaveri, Hitten P., DiLuna, Michael L., Grant, Ryan A., Hoshino, Kazunori
Publicado 2018

Child Neurology: Functional Reorganization Mediating Supplementary Motor Area Syndrome Recovery in Agenesis of the Corpus Callosum

por Obaid, Sami, Qureshi, Hanya M., Aljishi, Ayman, Shaikh, Neelam, Kundishora, Adam J., Bronen, Richard A., DiLuna, Michael, Damisah, Eyiyemisi C.
Publicado 2022

9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus

por Furey, Charuta, Antwi, Prince, Duran, Daniel, Timberlake, Andrew T., Nelson-Williams, Carol, Matouk, Charles C., DiLuna, Michael L., Günel, Murat, Kahle, Kristopher T.
Publicado 2018

Management of dynamic cervical kyphosis with dorsal epidural lipomatosis: a Hirayama disease variant? Illustrative case

por Kundishora, Adam J., Reeves, Benjamin C., Moreno-De-Luca, Andres, Hong, Christopher S., Robert, Stephanie M., Elsamadicy, Aladine A., Tuason, Dominick, DiLuna, Michael L.
Publicado 2023

Hypermutated phenotype in gliosarcoma of the spinal cord

por Hong, Christopher S., Kuzmik, Gregory A., Kundishora, Adam J., Elsamadicy, Aladine A., Koo, Andrew B., McGuone, Declan, Blondin, Nicholas A., DiLuna, Michael L., Erson-Omay, E. Zeynep
Publicado 2021

Malignant Cerebellar Edema Subsequent to Accidental Prescription Opioid Intoxication in Children

por Duran, Daniel, Messina, Robert D., Beslow, Lauren A., Montejo, Julio D., Karimy, Jason K., Gavankar Furey, Charuta, Sheridan, Alison D., Sze, Gordon, Yarman, Yanki, DiLuna, Michael L., Kahle, Kristopher T.
Publicado 2017

Comparison of epidemiology, treatments, and outcomes in pediatric versus adult ependymoma

por Elsamadicy, Aladine A, Koo, Andrew B, David, Wyatt B, Lee, Victor, Zogg, Cheryl K, Kundishora, Adam J, Hong, Christopher S, DeSpenza, Tyrone, Reeves, Benjamin C, Kahle, Kristopher T, DiLuna, Michael
Publicado 2020

De novo MYH9 mutation in congenital scalp hemangioma

por Fomchenko, Elena I., Duran, Daniel, Jin, Sheng Chih, Dong, Weilai, Erson-Omay, E. Zeynep, Antwi, Prince, Allocco, August, Gaillard, Jonathan R., Huttner, Anita, Gunel, Murat, DiLuna, Michael L., Kahle, Kristopher T.
Publicado 2018

Decline in the Volume of Structural Heart Procedures in the United States Due to the COVID-19 Pandemic

por Khalili, Houman, Lodhi, Hamza A., Luna, Michael, Hasan, Rani K., Banerjee, Subhash, Harvey, James E., Byrne, Timothy, Hanzel, George S., Abbas, Amr E., Bhatia, Nirmanmoh, Shreenivas, Satya S., Mathews, Adithya, Bansal, Priya, Morcos, Ramez, Maini, Brijeshwar
Publicado 2021

Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma

por Hong, Christopher S., Vasquez, Juan C., Kundishora, Adam J., Elsamadicy, Aladine A., Beckta, Jason M., Sule, Amrita, Marks, Asher M., Leelatian, Nalin, Huttner, Anita, Bindra, Ranjit S., DiLuna, Michael L., Kahle, Kristopher T., Erson-Omay, E. Zeynep
Publicado 2020

Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation

por Duran, Daniel, Jin, Sheng Chih, DeSpenza, Tyrone, Nelson-Williams, Carol, Cogal, Andrea G, Abrash, Elizabeth W, Harris, Peter C, Lieske, John C, Shimshak, Serena JE, Mane, Shrikant, Bilguvar, Kaya, DiLuna, Michael L, Günel, Murat, Lifton, Richard P, Kahle, Kristopher T
Publicado 2016

Educational impact of early COVID-19 operating room restrictions on neurosurgery resident training in the United States: A multicenter study

por Zhang, Justin K., del Valle, Armando, Ivankovic, Sven, Patel, Niel, Alexopoulos, Georgios, Khan, Maheen, Durrani, Sulaman, Patel, Mayur, Tecle, Najib El, Sujijantarat, Nanthiya, Jenson, Amanda V., Zammar, Samer G., Huntoon, Kristin, Goulart, Carlos R., Wilkinson, Brandon M., Bhimireddy, Sujit, Britz, Gavin W., DiLuna, Michael, Prevedello, Daniel M., Dinh, Dzung H., Mattei, Tobias A.
Publicado 2022

Plasma-based antigen persistence in the post-acute phase of SARS-CoV-2 infection

por Peluso, Michael J., Swank, Zoe N., Goldberg, Sarah A., Lu, Scott, Dalhuisen, Thomas, Borberg, Ella, Senussi, Yasmeen, Luna, Michael A., Song, Celina Chang, Clark, Alexus, Zamora, Andhy, Lew, Megan, Viswanathan, Badri, Huang, Beatrice, Anglin, Khamal, Hoh, Rebecca, Hsue, Priscila Y., Durstenfeld, Matthew S., Spinelli, Matthew A., Glidden, David V., Henrich, Timothy J., Kelly, J. Daniel, Deeks, Steven G., Walt, David R., Martin, Jeffrey N.
Publicado 2023

Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles

por Timberlake, Andrew T, Choi, Jungmin, Zaidi, Samir, Lu, Qiongshi, Nelson-Williams, Carol, Brooks, Eric D, Bilguvar, Kaya, Tikhonova, Irina, Mane, Shrikant, Yang, Jenny F, Sawh-Martinez, Rajendra, Persing, Sarah, Zellner, Elizabeth G, Loring, Erin, Chuang, Carolyn, Galm, Amy, Hashim, Peter W, Steinbacher, Derek M, DiLuna, Michael L, Duncan, Charles C, Pelphrey, Kevin A, Zhao, Hongyu, Persing, John A, Lifton, Richard P
Publicado 2016

Abstract 24: Two Locus Inheritance of Non-Syndromic Midline Craniosynostosis Via Rare SMAD6 and Common BMP2 Alleles

por Timberlake, Andrew T., Choi, Jungmin, Zaidi, Samir, Lu, Qiongshi, Nelson-Williams, Carol, Brooks, Eric D., Bilguvar, Kaya, Tikhonova, Irina, Mane, Shrikant, Yang, Jenny F., Sawh-Martinez, Rajendra, Persing, Sarah, Zellner, Elizabeth G., Loring, Erin, Chuang, Carolyn, Galm, Amy, Hashim, Peter W., Steinbacher, Derek, DiLuna, Michael L., Duncan, Charles C., Pelphrey, Kevin A., Zhao, Hongyu, Persing, John A., Lifton, Richard P.
Publicado 2017