Rapid ventricular overdrive pacing and other advanced flow-control techniques for the endovascular embolization of vein of galen malformations

por Baranoski, Jacob F., Catapano, Joshua S., Albuquerque, Felipe C., Abruzzo, Todd A.
Publicado 2023

Cerebral Cavernous Malformations: Review of the Genetic and Protein–Protein Interactions Resulting in Disease Pathogenesis

por Baranoski, Jacob F., Kalani, M. Yashar S., Przybylowski, Colin J., Zabramski, Joseph M.
Publicado 2016

Corrigendum: Cerebral Cavernous Malformations: Review of the Genetic and Protein–Protein Interactions Resulting in Disease Pathogenesis

por Baranoski, Jacob F., Kalani, M. Yashar S., Przybylowski, Colin J., Zabramski, Joseph M.
Publicado 2017

Coccidioidal meningitis with multiple aneurysms presenting with pseudo–subarachnoid hemorrhage: illustrative case

por Singh, Rohin, Srinivasan, Visish M., Catapano, Joshua S., DiDomenico, Joseph D., Baranoski, Jacob F., Lawton, Michael T.
Publicado 2021

Sterile Gelatin Film Reduces Cortical Injury Associated With Brain Tumor Re-Resection

por Przybylowski, Colin J, So, Veronica, DeTranaltes, Kaylee, Walker, Corey, Baranoski, Jacob F, Chapple, Kristina, Sanai, Nader
Publicado 2020

Telemedicine for Endovascular Neurosurgery Consultation During the COVID-19 Era: Patient Satisfaction Survey

por Majmundar, Neil, Ducruet, Andrew F., Wilkinson, D. Andrew, Catapano, Joshua S., Patel, Jimmy, Baranoski, Jacob F., Cole, Tyler S., Albuquerque, Felipe C.
Publicado 2022

METAP1 Mutation Is a Novel Candidate for Autosomal Recessive Intellectual Disability

por Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F., Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat
Publicado 2020

ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features

por Çağlayan, Ahmet Okay, Sezer, Rabia Gonul, Kaymakçalan, Hande, Ulgen, Ege, Yavuz, Taner, Baranoski, Jacob F., Bozaykut, Abdulkadir, Harmanci, Akdes Serin, Yalcin, Yalim, Youngblood, Mark W., Yasuno, Katsuhito, Bilgüvar, Kaya, Gunel, Murat
Publicado 2017

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP

por Çağlayan, Ahmet Okay, Tüysüz, Beyhan, Coşkun, Süleyman, Quon, Jennifer, Harmanci, Akdes Serin, Baranoski, Jacob F., Baran, Burçin, Erson-Omay, E. Zeynep, Henegariu, Octavian, Mane, Shrikant M., Bilgüvar, Kaya, Yasuno, Katsuhito, Günel, Murat
Publicado 2016