Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Omar Niss"'
Autor:
Emily R. Meier, Susan E. Creary, Matthew M. Heeney, Min Dong, Abena O. Appiah-Kubi, Stephen C. Nelson, Omar Niss, Connie Piccone, Maa-Ohui Quarmyne, Charles T. Quinn, Kay L. Saving, John P. Scott, Ravi Talati, Teresa S. Latham, Amanda Pfeiffer, Lisa M. Shook, Alexander A. Vinks, Adam Lane, Patrick T. McGann
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-14 (2020)
Abstract Background Sickle cell disease (SCD) is a severe and devastating hematological disorder that affects over 100,000 persons in the USA and millions worldwide. Hydroxyurea is the primary disease-modifying therapy for the SCD, with proven benefi
Externí odkaz:
https://doaj.org/article/f4848c1e5cb84d1ca9d6331a034404f0
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/840996a63d2c4519a193f1ac68e710b4
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Hereditary spherocytosis (HS) is the most common red blood cell (RBC) membrane disorder causing hereditary hemolytic anemia. Patients with HS have defects in the genes coding for ankyrin (ANK1), band 3 (SLC4A1), protein 4.2 (EPB42), and α (SPTA1) or
Externí odkaz:
https://doaj.org/article/ad840012f1744b04820b5b66c13c0ebd
Autor:
Omar Niss, Jon Detterich, John C. Wood, Thomas D. Coates, Punam Malik, Michael D. Taylor, Charles T. Quinn
Publikováno v:
Blood. 140:1322-1324
Cardiovascular disease is a major cause of mortality in patients with sickle cell disease (SCD). Niss et al previously reported that cardiac magnetic resonance in 25 patients showed universal myocardial fibrosis, which they correlated with increased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7631c3a5bcd8199ef1033dd2e5b08735
https://doi.org/10.1182/blood.2021015303
https://doi.org/10.1182/blood.2021015303
Autor:
Kristine Karkoska, Amanda Pfeiffer, Dean W. Beebe, Charles T. Quinn, Omar Niss, Patrick T. McGann
Publikováno v:
American journal of hematology. 97(10)
Children with sickle cell disease (SCD) who began hydroyxurea before age five years scored no differently on a measure of cognitive funciton than age, sex, and race-matched unaffected peers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d78f936cadd1e1281798948158e50d7
https://pubmed.ncbi.nlm.nih.gov/35836401
https://pubmed.ncbi.nlm.nih.gov/35836401
Autor:
Patrick T. McGann, Amanda Pfeiffer, Charles T. Quinn, Omar Niss, Min Dong, Alexander A. Vinks, Kristine Karkoska
Publikováno v:
Am J Hematol
Neurologic complications are common in patients with sickle cell anemia (SCA), but conventional tools such as MRI and transcranial Doppler ultrasonography (TCD) do not fully assess cerebrovascular pathology. Cerebral tissue oximetry measures mixed ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99584e53aab8aa5108a3537f0e00197d
https://doi.org/10.1002/ajh.26120
https://doi.org/10.1002/ajh.26120
Autor:
Abena Appiah-Kubi, Seethal A Jacob, Matthew M. Heeney, Clark Brown, Susan E. Creary, Christine R Hollenkamp, Emily Riehm Meier, Omar Niss, Connie M. Piccone, Maa-Ohui Quarmyne, Charles T. Quinn, Allison Remiker, Kay L Saving, Min Dong, Patrick T. McGann
Publikováno v:
Blood. 140:5416-5417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::304204b52abb6d10c0597d5f212752b4
https://doi.org/10.1182/blood-2022-158623
https://doi.org/10.1182/blood-2022-158623
Autor:
Hisham Abdel-Azim, Suchitra S. Acharya, Anurag K. Agrawal, Maha Al-Ghafry, Carl E. Allen, Seema Amin, Mark P. Atlas, Rochelle Bagatell, Lionel Blanc, Francine Blei, James B. Bussel, William L. Carroll, James A. Connelly, Jeffrey S. Dome, Brian M. Dulmovits, Olive S. Eckstein, Caitlin W. Elgarten, Mohamed Tarek Elghetany, Noah Federman, Carolyn Fein Levy, James Feusner, Jonathan D. Fish, Adriana Fonseca, Jason L. Freedman, Debra L. Friedman, Derek Hanson, Nobuko Hijiya, Inga Hofmann, Mary S. Huang, Ionela Iacobas, Cassandra D. Josephson, Rachel Kessel, Eugene Khandros, Julie Krystal, Janet L. Kwiatkowski, Philip Lanzkowsky, Ann Leahey, Jeffrey M. Lipton, Catherine McGuinn, Rajen J. Mody, Amy Nadel, Michelle Nash, Omar Niss, Thomas A. Olson, Pallavi M. Pillai, Jacquelyn M. Powers, Josef T. Prchal, Michael A. Pulsipher, Charles T. Quinn, Miriam Radinsky, Arlene Redner, Susan R. Rheingold, Susmita N. Sarangi, Amish Shah, Jordan A. Shavit, Christine M. Smith, Elizabeth Sokol, Kathryn S. Sutton, Tsewang Tashi, David T. Teachey, Anshul Vagrecha, Adrianna Vlachos, Kelly Walkovich, Anne B. Warwick, Howard J. Weinstein, Katrina Winsnes, Lawrence C. Wolfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9ce43d5bfb90ec0781092e5f0e1210
https://doi.org/10.1016/b978-0-12-821671-2.00046-5
https://doi.org/10.1016/b978-0-12-821671-2.00046-5
Publikováno v:
The Journal of Pediatrics. 226:303-305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5959d4f055cca65638ed890efa6b6b7b
https://doi.org/10.1016/j.jpeds.2020.07.051
https://doi.org/10.1016/j.jpeds.2020.07.051