Zobrazeno 1 - 10
of 120
pro vyhledávání: '"W. Oliver Tobin"'
Autor:
Judit M. Perez Ortiz, Karthik Muthusamy, W. Oliver Tobin, Ralitza Gavrilova, Margot A. Cousin, Radhika Dhamija
Publikováno v:
Journal of Rare Diseases, Vol 3, Iss 1, Pp 1-5 (2024)
Abstract Introduction LMNB1-related autosomal dominant leukodystrophy (ADLD) is a slowly progressive neurodegenerative disorder caused by overexpression of LMNB1. We retrospectively reviewed charts of all ADLD patients seen at Mayo Clinic. Methods Al
Externí odkaz:
https://doaj.org/article/fee64c72926d496d85722fdda5e4b36d
Autor:
Samantha A. Banks, Paul Decker, Eoin P. Flanagan, Anastasia Zekeridou, Ronald S. Go, Jithma P. Abeykoon, Gaurav Goyal, Jason R. Young, Matthew J. Koster, Robert Vassallo, Jay H. Ryu, Caroline J. Davidge-Pitts, Aishwarya Ravindran, Julio C. Sartori Valinotti, N. Nora Bennani, Mithun V. Shah, Karen L. Rech, Corrie R. Bach, Jeanette E. Eckel-Passow, W. Oliver Tobin, the Mayo Clinic-University of Alabama at Birmingham Histiocytosis Working Group and Center for Multiple Sclerosis and Autoimmune Neurology at Mayo Clinic
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-4 (2024)
Externí odkaz:
https://doaj.org/article/0ac0c9b2c4ed4e4a9c9aaea6d8fa366a
Autor:
Nabeela Nathoo, Joon H. Uhm, Alyx B. Porter, Julie Hammack, Kurt A. Jaeckle, Maciej M. Mrugala, Brian A. Crum, Eoin P. Flanagan, Sean J. Pittock, Gaurav Goyal, Jason R. Young, Matthew J. Koster, Robert Vassallo, Jay H. Ryu, Caroline J. Davidge-Pitts, Corrie Bach, Aishwarya Ravindran, Julio C. Sartori Valinotti, N. Nora Bennani, Jithma P. Abeykoon, Mithun V. Shah, C. Christopher Hook, Karen L. Rech, Ronald S. Go, W. Oliver Tobin, Mayo Clinic-University of Alabama at Birmingham Histiocytosis Working Group
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-6 (2024)
Externí odkaz:
https://doaj.org/article/d4294af31f2d4566a2da10f63976eafc
Autor:
Mahboubeh Fereidan‐Esfahani, Paul A Decker, Stephen D. Weigand, Alfonso S. Lopez Chiriboga, Eoin P Flanagan, Jan‐Mendelt Tillema, Claudia F Lucchinetti, Jeanette E. Eckel‐Passow, W. Oliver Tobin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 9, Pp 1544-1555 (2023)
Abstract Objective To describe demographic, clinical, and radiographic features of tumefactive demyelination (TD) and identify factors associated with severe attacks and poor outcomes. Methods Retrospective review of TD cases seen at Mayo Clinic, 199
Externí odkaz:
https://doaj.org/article/6f925103615a4632bed5985acb7c7397
Autor:
Marie Hu, Gaurav Goyal, Jithma P. Abeykoon, Aldo A. Acosta-Medina, Gordan J. Ruan, Jason R. Young, Aishwarya Ravindran, N. Nora Bennani, Mithun V. Shah, Robert Vassallo, Jay H. Ryu, Caroline J. Davidge-Pitts, Matthew J. Koster, W. Oliver Tobin, Julio C. Sartori-Valinotti, Karen L. Rech, Ronald S. Go
Publikováno v:
Blood Cancer Journal, Vol 12, Iss 6, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/95caf073631847d49e330bb2136547ed
Autor:
Karan L. Chohan, Jithma P. Abeykoon, Jason R. Young, W. Oliver Tobin, Mathew J. Koster, Mithun V. Shah, Jay H. Ryu, Robert Vassallo, Karen L. Rech., Aishwarya Ravindran, Gaurav Goyal, Ronald S. Go, N. Nora Bennani
Publikováno v:
Haematologica, Vol 108, Iss 6 (2022)
Externí odkaz:
https://doaj.org/article/f5b61c39bac74aecac9061d71360e22b
Autor:
Christopher J. Boes, MD, James P. Klaas, MD, W. Oliver Tobin, MB, BCh, BAO, PhD, Eoin P. Flanagan, MB, BCh, Andrew McKeon, MB, BCh, MD, Sherri A. Braksick, MD, David B. Burkholder, MD, Derek W. Stitt, MD, Jeremy K. Cutsforth-Gregory, MD
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 5, Iss 4, Pp 701-719 (2021)
Externí odkaz:
https://doaj.org/article/7351cf0ec8604eab973f210c042db0cd
Autor:
Siobhan Delaney, Ged O'Connor, William Reardon, Stephen J. X. Murphy, Sean Tierney, Barbara M. Ryan, Holly Delaney, Colin P. Doherty, Michael Guiney, Paul Brennan, W. Oliver Tobin, Dominick J. H. McCabe
Publikováno v:
Frontiers in Neurology, Vol 9 (2019)
Background: Alagille syndrome (AGS) is an autosomal-dominant, multisystem disorder caused by mutations in the JAG1 gene.Case Description: A 34-year-old man was referred to our service 10 years ago with focal seizures with impaired awareness and trans
Externí odkaz:
https://doaj.org/article/ebc4e3addb0c4beab650cd53bebec8b2
Publikováno v:
Journal of Central Nervous System Disease, Vol 2009, Iss 1, Pp 19-22 (2009)
Externí odkaz:
https://doaj.org/article/02561f3c6f2d4512aac4ab03d5b03bde
Autor:
Samantha A. Banks, M. Tariq Bhatti, Ronald S. Go, Jithma P. Abeykoon, Aldo A. Acosta-Medina, Antonious Z. Hazim, Gaurav Goyal, Jason R. Young, Matthew J. Koster, Robert Vassallo, Jay H. Ryu, Caroline J. Davidge-Pitts, Aishwarya Ravindran, Julio C. Sartori Valinotti, N. Nora Bennani, Mithun V. Shah, Karen L. Rech, James A. Garrity, W. Oliver Tobin
Publikováno v:
Ophthalmology. 130:77-86
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a10af16ff7d0fc53311c44356d6ab75c
https://doi.org/10.1016/j.ophtha.2022.07.031
https://doi.org/10.1016/j.ophtha.2022.07.031