Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Thomas V. Adamkiewicz"'
Autor:
Carlos S. Alvarado, Rommel Yanac-Avila, Evelyn Marron-Veria, José Málaga-Zenteno, Thomas V. Adamkiewicz
Publikováno v:
Anales de la Facultad de Medicina. 83:65-69
Deficiencia de hierro (DH) y anemia ferropénica (AF) continúan siendo problemas de salud de magnitud en el mundo y afectan especialmente a niños preescolares y mujeres embarazadas. Este artículo tiene como objetivos: a) Describir las pruebas de l
Publikováno v:
Pediatrics. 147
* Abbreviations: ISSOP — : International Society for Social Pediatrics and Child Health UN — : United Nations Similar to previous reports,1–12 the latest annual United Nations (UN) Report on Children and Armed Conflict identified 10 173 child c
Autor:
Inci Yildirim, Stephanie Thomas, Monica M. Farley, Folashade Omole, Marianne McPherson Yee, Peter A. Lane, Kristina Lai, Amy Tunali, Thomas V. Adamkiewicz
Publikováno v:
Blood. 138:763-763
Before prophylactic antibiotic use, approximately 1/10 children Figure 1 Figure 1. Disclosures No relevant conflicts of interest to declare.
Autor:
Ernest Alema-Mensah, Dennis Bryan, Jason Payne, Kathy Pines, Chad Evans, Adel Driss, Thomas V. Adamkiewicz, Marlene Garcia, Tennille Leak-Johnson, Melvin R. Echols, Marques Harvey, Jan Morgan-Billingslea, Mohamed Mubasher, Herman A. Taylor, Jennifer A Afranie-Sakyi, Teclemichael Tewolde, Eric Flenaugh, Folashade Omole, Olusola Gbinigie, Eric Y. Chang, Judith Volcy, Charlye D. Majett, Deborah A. Sundal, Shira Krebs
Publikováno v:
Blood
A diagnosis of SCD is considered to be at risk for COVD19. To further define the association between SCD and infection with COVID-19, we estimated risk, by comparing presence or absence of COVID19 infections in individuals with and without SCD admitt
Publikováno v:
Pediatric Blood & Cancer. 62:2076-2081
Background Approximately 10–20% of children with sickle cell disease (SCD) develop stroke, but few consistent national estimates of the stroke burden for children with SCD exist. The purpose of this study is to determine the proportion of diagnosed
Publikováno v:
Blood. 134:4813-4813
Iron deficiency anemia (IDA) screening in children, and its treatment is standard in general pediatrics. IDA has been linked to developmental concerns. However, iron supplementation recently has been shown to have risks in resource limited environmen
Publikováno v:
Blood. 132:3574-3574
Although SCD-related mortality has improved over the last 3 decades, mortality from acute pulmonary causes remains relatively unchanged.(Payne, 2017)Acute chest syndrome (ACS) occurs in patients with SCD of all ages and influenza infection is one of
Autor:
Kuang-Yueh Chiang, S.L. Staba, John E. Wagner, Michael Boyer, Lakshmanan Krishnamurti, Andrew M. Yeager, Ann E. Haight, K. Scott Baker, Paul Szabolcs, John R. Wingard, Thomas V. Adamkiewicz, Joan Kurtzberg, Amos Kedar
Publikováno v:
Pediatric Transplantation. 11:641-644
UCBT was performed in seven children with SCD and stroke (HLA match 4/6 n=5; 5/6 n=2). Four received myeloablative regimens (BU, CY, ATG plus FLU in one patient). One had primary graft failure, three had sustained engraftment, two with grade III-IV G
Autor:
Thomas V. Adamkiewicz, B. Sleight, Peter A. Lane, Keith M. Sullivan, A. Haight, Barry Eggleston, Lewis L. Hsu, N. Kamani, John T. Horan, Roger Giller, Rupa Redding-Lallinger, Alexis A. Thompson, T. B. Moore, George R. Buchanan, J. E. Levine, J. E. Sanders, S. Donfield, Sandie Edwards, David A. Margolis, R. Dickerhoff, S. A. Feig, J. P. Scott, Mark C. Walters, S. C. Davies, Zora R. Rogers, Melinda Patience, I. A.G. Roberts, K. Ohene-Frempong
Publikováno v:
British Journal of Haematology. 136:673-676
Although haematopoietic cell transplantation (HCT) is curative for sickle cell anaemia (SCA), concerns about its short- and long-term toxicities limit its application. A potential toxicity is an adverse effect on growth. To identify an HCT growth eff
Autor:
Scott D. Grosse, Thomas V. Adamkiewicz, Djesika D. Amendah, Sunetra Gupta, Thomas N. Williams, Frédéric B. Piel
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 18(3)
Purpose Our objective was to compare observed and expected genotype proportions from newborn screening surveys of structural hemoglobin variants. Methods We conducted a systematic review of newborn screening surveys of hemoglobins S and C in Africa a