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pro vyhledávání: '"Matthew J. Barkovich"'
Autor:
Matthew J. Barkovich
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1123 (2022)
Neurodevelopmental disorders, including neuronal migration disorders, are best understood in the context of altered normal development. Neurons normally migrate from their site of origin to their (usually cortical) destination using a wide range of m
Externí odkaz:
https://doaj.org/article/2fc390408dd5488fb7634578e83e7900
Autor:
Ali Nabavizadeh, Matthew J Barkovich, Ali Mian, Van Ngo, Anahita Fathi Kazerooni, Javier E Villanueva-Meyer
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 37, Iss , Pp 100886- (2023)
Imaging plays a central role in neuro-oncology including primary diagnosis, treatment planning, and surveillance of tumors. The emergence of quantitative imaging and radiomics provided an uprecedented opportunity to compile mineable databases that ca
Externí odkaz:
https://doaj.org/article/c32b5a9491e840f3906bdf60bd399772
Autor:
Matthew J. Barkovich, Jacob S. Young, Jing Li, Andrew J Gogos, Mitchel S. Berger, Matheus P. Pereira, Shawn L. Hervey-Jumper, Ramin A. Morshed
Publikováno v:
Journal of Neurosurgery. 135:989-997
OBJECTIVETumor proximity to the ventricle and ventricular entry (VE) during surgery have both been associated with worse prognoses; however, the interaction between these two factors is poorly understood. Given the benefit of maximal tumor resection,
Autor:
Aditya Karandikar, Agnieszka Solberg, Alice Fung, Amie Y. Lee, Amina Farooq, Amy C. Taylor, Amy Oliveira, Anand Narayan, Andi Senter, Aneesa Majid, Angela Tong, Anika L. McGrath, Anjali Malik, Ann Leylek Brown, Anne Roberts, Arthur Fleischer, Beth Vettiyil, Beth Zigmund, Brian Park, Bruce Curran, Cameron Henry, Camilo Jaimes, Cara Connolly, Caroline Robson, Carolyn C. Meltzer, Catherine H. Phillips, Christine Dove, Christine Glastonbury, Christy Pomeranz, Claudia F.E. Kirsch, Constantine M. Burgan, Courtney Scher, Courtney Tomblinson, Cristina Fuss, Cynthia Santillan, Dania Daye, Daniel B. Brown, Daniel J. Young, Daniel Kopans, Daniel Vargas, Dann Martin, David Thompson, David W. Jordan, Deborah Shatzkes, Derek Sun, Domenico Mastrodicasa, Elainea Smith, Elena Korngold, Elizabeth H. Dibble, Elizabeth K. Arleo, Elizabeth M. Hecht, Elizabeth Morris, Elizabeth P. Maltin, Erin A. Cooke, Erin Simon Schwartz, Evan Lehrman, Faezeh Sodagari, Faisal Shah, Florence X. Doo, Francesca Rigiroli, George K. Vilanilam, Gina Landinez, Grace Gwe-Ya Kim, Habib Rahbar, Hailey Choi, Harmanpreet Bandesha, Haydee Ojeda-Fournier, Ichiro Ikuta, Irena Dragojevic, Jamie Lee Twist Schroeder, Jana Ivanidze, Janine T. Katzen, Jason Chiang, Jeffers Nguyen, Jeffrey D. Robinson, Jennifer C. Broder, Jennifer Kemp, Jennifer S. Weaver, Jesse M. Conyers, Jessica B. Robbins, Jessica R. Leschied, Jessica Wen, Jocelyn Park, John Mongan, Jordan Perchik, José Pablo Martínez Barbero, Jubin Jacob, Karyn Ledbetter, Katarzyna J. Macura, Katherine E. Maturen, Katherine Frederick-Dyer, Katia Dodelzon, Kayla Cort, Kelly Kisling, Kemi Babagbemi, Kevin C. McGill, Kevin J. Chang, Kimberly Feigin, Kimberly S. Winsor, Kimberly Seifert, Kirang Patel, Kristin K. Porter, Kristin M. Foley, Krupa Patel-Lippmann, Lacey J. McIntosh, Laura Padilla, Lauren Groner, Lauren M. Harry, Lauren M. Ladd, Lisa Wang, Lucy B. Spalluto, M. Mahesh, M. Victoria Marx, Mark D. Sugi, Marla B.K. Sammer, Maryellen Sun, Matthew J. Barkovich, Matthew J. Miller, Maya Vella, Melissa A. Davis, Meridith J. Englander, Michael Durst, Michael Oumano, Monica J. Wood, Morgan P. McBee, Nancy J. Fischbein, Nataliya Kovalchuk, Neil Lall, Neville Eclov, Nikhil Madhuripan, Nikki S. Ariaratnam, Nina S. Vincoff, Nishita Kothary, Noushin Yahyavi-Firouz-Abadi, Olga R. Brook, Orit A. Glenn, Pamela K. Woodard, Parisa Mazaheri, Patricia Rhyner, Peter R. Eby, Preethi Raghu, Rachel F. Gerson, Rina Patel, Robert L. Gutierrez, Robyn Gebhard, Rochelle F. Andreotti, Rukya Masum, Ryan Woods, Sabala Mandava, Samantha G. Harrington, Samir Parikh, Sammy Chu, Sandeep S. Arora, Sandra M. Meyers, Sanjay Prabhu, Sara Shams, Sarah Pittman, Sejal N. Patel, Shelby Payne, Steven W. Hetts, Tarek A. Hijaz, Teresa Chapman, Thomas W. Loehfelm, Titania Juang, Toshimasa J. Clark, Valeria Potigailo, Vinil Shah, Virginia Planz, Vivek Kalia, Wendy DeMartini, William P. Dillon, Yasha Gupta, Yilun Koethe, Zachary Hartley-Blossom, Zhen Jane Wang, Geraldine McGinty, Adina Haramati, Laveil M. Allen, Pauline Germaine
Publikováno v:
Clinical imaging. 93
Autor:
Matthew J. Barkovich, Taemin Oh, Anthony T. Lee, John K. Yue, Kunal P. Raygor, Ethan A. Winkler, Alex Y. Lu, Ryan R L Phelps, Harry Hollander
Publikováno v:
Journal of Clinical Neuroscience. 80:282-289
Coccidioidomycosis exposure is common in the southwest United States and northern Mexico. Dissemination to the meninges is the most severe form of progression. Although ischemic strokes are well-reported in these patients, other cerebrovascular compl
Autor:
Matthew J. Barkovich, A. J. Barkovich
Publikováno v:
Neuroimaging Clinics of North America. 29:325-337
Normal brain development is best evaluated by MR imaging in the fetal and pediatric patient. As the developing brain grows, myelinates, and sulcates rapidly, understanding the normal appearance of the brain throughout development is critical. The fet
Autor:
Cassie Kline, Leo P. Sugrue, Orit A. Glenn, Ryan M. Nillo, Sabine Mueller, Christine M. Glastonbury, Anders M. Dale, Christopher P. Hess, Rahul S. Desikan, Matthew J. Barkovich, William P. Dillon, Duan Xu, A. James Barkovich, Terry L. Jernigan, Chin Hong Tan, Yi Li
Publikováno v:
Barkovich, MJ; Tan, CH; Nillo, RM; Li, Y; Xu, D; Glastonbury, CM; et al.(2018). Abnormal Morphology of Select Cortical and Subcortical Regions in Neurofibromatosis Type 1. Radiology, 289(2), 499-508. doi: 10.1148/radiol.2018172863. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/5c27k8p8
PURPOSE: To evaluate whether patients with neurofibromatosis type 1 (NF1)—a multisystem neurodevelopmental disorder with myriad imaging manifestations, including focal transient myelin vacuolization within the deep gray nuclei, brainstem, and cereb
Autor:
Matthew J. Barkovich, Ramin A. Morshed, Andrew J Gogos, Matheus P. Pereira, Jacob S. Young, Jing Li, Shawn L. Hervey-Jumper, Mitchel S. Berger
Publikováno v:
Neurosurgery. 67
Autor:
Claude Lepage, Alan C. Evans, Kiho Im, Caitlin K. Rollins, Lana Vasung, Hyuk Jin Yun, Hao Huang, Jennings Zhang, Clemente Velasco-Annis, Simon K. Warfield, Teddy Corcoran, Patricia Ellen Grant, Chenying Zhao, Matthew J. Barkovich, Ali Gholipour
Publikováno v:
Cereb Cortex
The relationship between structural changes of the cerebral cortex revealed by Magnetic Resonance Imaging (MRI) and gene expression in the human fetal brain has not been explored. In this study, we aimed to test the hypothesis that relative regional
Autor:
Rahul S. Desikan, Jennifer S. Yokoyama, Nicholas J. Schmansky, Daniel Cuneo, William P. Dillon, Chun Chieh Fan, Matthew J. Barkovich, Ryan M. Nillo, Yi Li, Bruce L. Miller, Celeste M. Karch, Chin Hong Tan, Christopher P. Hess, Nicholas T. Olney, Ole A. Andreassen, Luke W. Bonham, Iris J. Broce, Terry L. Jernigan, Christine M. Glastonbury, A. James Barkovich, Leo P. Sugrue, Anders M. Dale, Aimee W. Kao, Orit A. Glenn, Bruce Fischl
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific reports, vol 8, iss 1
Scientific Reports
Li, Y; Barkovich, MJ; Karch, CM; Nillo, RM; Fan, CC; Broce, IJ; et al.(2018). Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex. Scientific Reports, 8(1). doi: 10.1038/s41598-018-31075-4. UCSF: Retrieved from: http://www.escholarship.org/uc/item/3m61c5mt
Li, Yi; Barkovich, Matthew J; Karch, Celeste M; Nillo, Ryan M; Fan, Chun-Chieh; Broce, Iris J; et al.(2018). Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex. Scientific Reports, 8(1). doi: 10.1038/s41598-018-31075-4. UCSF: UCSF Library. Retrieved from: http://www.escholarship.org/uc/item/4zk6w74d
Scientific reports, vol 8, iss 1
Scientific Reports
Li, Y; Barkovich, MJ; Karch, CM; Nillo, RM; Fan, CC; Broce, IJ; et al.(2018). Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex. Scientific Reports, 8(1). doi: 10.1038/s41598-018-31075-4. UCSF: Retrieved from: http://www.escholarship.org/uc/item/3m61c5mt
Li, Yi; Barkovich, Matthew J; Karch, Celeste M; Nillo, Ryan M; Fan, Chun-Chieh; Broce, Iris J; et al.(2018). Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex. Scientific Reports, 8(1). doi: 10.1038/s41598-018-31075-4. UCSF: UCSF Library. Retrieved from: http://www.escholarship.org/uc/item/4zk6w74d
Tuberous sclerosis complex (TSC), a heritable neurodevelopmental disorder, is caused by mutations in the TSC1 or TSC2 genes. To date, there has been little work to elucidate regional TSC1 and TSC2 gene expression within the human brain, how it change