Zobrazeno 1 - 10
of 704
pro vyhledávání: '"J, Fitzgibbon"'
Autor:
Taylor McManus, BS, MS, Noa G. Holtzman, MD, Aaron Zhao, BS, Chantal Cousineau-Krieger, MD, Susan Vitale, PhD, MHS, Edmond J. FitzGibbon, MD, Debbie Payne, BS, MBA, Janine Newgen, COT, Celestina Igbinosun, BSN, RN, Annie P. Im, MD, Cody Peer, MS, PhD, William Douglas Figg, Sr., Pharm D, Edward W. Cowen, MD, Jacqueline W. Mays, DDS, PhD, Steven Pavletic, MD, PhD, M.Teresa Magone, MD
Publikováno v:
Ophthalmology Science, Vol 5, Iss 1, Pp 100627- (2025)
Objective: To investigate the effects of oral baricitinib on ocular surface disease (OSD) in patients with chronic graft-versus-host disease (cGVHD). Design: Prospective phase 1 to 2 single institution trial. Subjects: Eighteen patients with ocular g
Externí odkaz:
https://doaj.org/article/877ccca9a34547dd8a20cab8fdca5d2a
Publikováno v:
Data in Brief, Vol 39, Iss , Pp 107449- (2021)
This article reports quantitative measurements of intracranial volume, optic canal area, and peripapillary retinal nerve fiber layer (RNFL) for a cohort of 124 patients with craniofacial fibrous dysplasia/McCune-Albright Syndrome (FD/MAS), previously
Externí odkaz:
https://doaj.org/article/7d871158b9f94d4c9201c0d84cad3e93
Autor:
W. Grey, A. Rio-Machin, P. Casado-Izquierdo, E. Gronroos, S. Ali, J. Miettinen, F. Bewicke-Copley, A. Parsons, C. Heckman, C. Swanton, P. Cutillas, J. Gribben, J. Fitzgibbon, D. Bonnet
Publikováno v:
HemaSphere, Vol 6, Pp 305-306 (2022)
Externí odkaz:
https://doaj.org/article/55d35c4042014e1d9fe8b1d72d07b292
Autor:
James J. Fitzgibbon, Patrick Heindel, Jessica D. Feliz, Eva Rouanet, Winona Wu, Cindy Huynh, Dirk M. Hentschel, Michael Belkin, C. Keith Ozaki, Mohamad A. Hussain
Publikováno v:
Journal of Vascular Surgery. 77:1788-1796
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Vascular Surgery. 77:e313-e314
Autor:
Patrick Heindel, Tanujit Dey, James J. Fitzgibbon, Dirk Hentschel, Michael Belkin, C. Keith Ozaki, Mohamad A. Hussain
Publikováno v:
Journal of Vascular Surgery. 77:e315-e316
Autor:
Marcus Y. Chen, Edmond J. FitzGibbon, William A. Gahl, Skand Shekhar, Fady Hannah-Shmouni, Beth Solomon, Rahul Dave, Leora E. Comis, Juvianee Estrada-Veras, Kevin O'Brien, Bernadette R. Gochuico
Publikováno v:
Journal of the National Comprehensive Cancer Network. 19:1312-1318
Adult-onset histiocytoses (AOH), primarily Rosai-Dorfman disease (RDD), Erdheim-Chester Disease (ECD), and adult Langerhans cell histiocytosis (ALCH), are a group of related histiocytic neoplastic disorders featuring multisystemic manifestations. The
Autor:
Flavia M. Facio, Bryn D. Webb, Alan Ma, Christopher Troedson, Irini Manoli, Carmen C. Brewer, Christopher K. Zalewski, Elizabeth C. Engle, Carol Van Ryzin, Audrey Thurm, Paul R. Lee, Timothy James Maarup, Malin Kvarnung, Edmond J. FitzGibbon, Hans Ulrik Møller, Camilo Toro, Scott M. Paul, Glad Ragnhild, Jayne Antony, Omar A. Abdul-Rahman, David G. Hunter, Janice S. Lee, Katrine V. Wirgenes, Dorte Ancher Larsen, Mary C. Whitman, Caroline D. Robson, Wai-Man Chan, Kelly A. King, Tanya J. Lehky, Francis S. Collins, Brenda J. Barry, Sarah MacKinnon, Angela Delaney, Emma Tham, Konstantinia Almpani, Ethylin Wang Jabs
Publikováno v:
Whitman, M C, Barry, B J, Robson, C D, Facio, F M, Van Ryzin, C, Chan, W M, Lehky, T J, Thurm, A, Zalewski, C, King, K A, Brewer, C, Almpani, K, Lee, J S, Delaney, A, FitzGibbon, E J, Lee, P R, Toro, C, Paul, S M, Abdul-Rahman, O A, Webb, B D, Jabs, E W, Moller, H U, Larsen, D A, Antony, J H, Troedson, C, Ma, A, Ragnhild, G, Wirgenes, K V, Tham, E, Kvarnung, M, Maarup, T J, MacKinnon, S, Hunter, D G, Collins, F S, Manoli, I & Engle, E C 2021, ' TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy ', Human Genetics, vol. 140, no. 12, pp. 1709-1731 . https://doi.org/10.1007/s00439-021-02379-9
Microtubules are formed from heterodimers of alpha- and beta-tubulin, each of which has multiple isoforms encoded by separate genes. Pathogenic missense variants in multiple different tubulin isoforms cause brain malformations. Missense mutations in