Russell E. Ware - Concepedia

Author

Russell E. Ware

Duke Medical Center ORCID

Also Known As

Manci, Elizabeth A., R E Ware, R E. Ware, R WARE, R Ware, R. E. WARE, R. E. Ware, R. Ware, R.E. Ware, R. E. WARE

596

Publications

24.3K

Citations

H-Index

237

Concepts

All Affiliations

Duke Medical Center Cincinnati Children's Hospital Medical Center St. Jude Children's Research Hospital Duke University Hospital Duke University

About

Russell E. Ware is an author at Duke Medical Center specializing in medicine, hematology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Health Sciences	18	24	1.4K
2	Education	3	3	87
3	Engineering	3	3	390
4	Arts	1	1	270
5	Language Studies	1	1	270

Russell E. Ware

242

Publications

18.2K

Citations

H-Index

Page 1

	Year	Citations
Causes and Outcomes of the Acute Chest Syndrome in Sickle Cell Disease Elliott Vichinsky, Lynne Neumayr, Ann N. Earles, New England Journal of Medicine	2000	1.2K
Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG) Winfred C. Wang, Russell E. Ware, Scott T. Miller, The Lancet Baby HugPediatric EpidemiologyPediatric HematologySickle-cell AnaemiaHematology	2011	772
A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease Elliott Vichinsky, Carolyn Hoppe, Kenneth I. Ataga, New England Journal of Medicine	2019	581
Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial Russell E. Ware, Barry R. Davis, William H. Schultz, The Lancet Pediatric HematologyHematologyNeurological MonitoringSickle CellHemostasis	2015	496
Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group. Thomas R. Kinney, Ronald W. Helms, Erin E. O’Branski, PubMed	1999	422
Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) Russell E. Ware, Ronald W. Helms Blood	2012	376
R2* magnetic resonance imaging of the liver in patients with iron overload Jane S. Hankins, M. Beth McCarville, Ralf B. Loeffler, Blood	2009	370
Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa Léon Tshilolo, George Tomlinson, Thomas N. Williams, New England Journal of Medicine	2018	354
Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly) Katrin Hoffmann, Christine Karin Dreger, Ada L. Olins, Nature Genetics Lamin B ReceptorGranulocyteCell SignalingGeneticsGenetic Disorder	2002	346
Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Genetics in Medicine Translational MedicineBiochemistryInherited Metabolic DiseaseGlycobiologyPediatrics	2001	346

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