Z R Rogers
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Explore the profile of Z R Rogers including associated specialties, affiliations and a list of published articles.
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35
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703
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Recent Articles
1.
Eggleston B, Patience M, Edwards S, Adamkiewicz T, Buchanan G, Davies S, et al.
Br J Haematol
. 2007 Jan;
136(4):673-6.
PMID: 17223910
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...
2.
3.
Walters M, Patience M, Leisenring W, Rogers Z, Aquino V, Buchanan G, et al.
Biol Blood Marrow Transplant
. 2002 Jan;
7(12):665-73.
PMID: 11787529
A multicenter investigation of allogeneic bone marrow transplantation for children with sickle cell disease was conducted that included 27 European and North American transplant centers. Fifty-nine patients who ranged in...
4.
Berger R, Billups K, Brock G, Broderick G, Dhabuwala C, Goldstein I, et al.
Int J Impot Res
. 2002 Jan;
13 Suppl 5:S39-43.
PMID: 11781746
Purpose: Patients with priapism often develop permanent erectile dysfunction and personal sexual distress. This report is intended to help educate the public by reviewing the varied definitions and classifications of...
5.
Wang W, Wynn L, Rogers Z, Scott J, Lane P, Ware R
J Pediatr
. 2001 Dec;
139(6):790-6.
PMID: 11743503
Objective: Hydroxyurea improves hematologic values and decreases vaso-occlusive complications in adults and children with sickle cell anemia (SCA), but has not been tested in infants before the onset of chronic...
6.
Evans W, Hon Y, Bomgaars L, Coutre S, Holdsworth M, Janco R, et al.
J Clin Oncol
. 2001 Apr;
19(8):2293-301.
PMID: 11304783
Purpose: To assess thiopurine S-methyltransferase (TPMT) phenotype and genotype in patients who were intolerant to treatment with mercaptopurine (MP) or azathioprine (AZA), and to evaluate their clinical management. Patients And...
7.
Walters M, Storb R, Patience M, Leisenring W, Taylor T, Sanders J, et al.
Blood
. 2000 Mar;
95(6):1918-24.
PMID: 10706855
Fifty children who had symptomatic sickle cell disease received matched sibling marrow allografts between September 1991 and March 1999, with Kaplan-Meier probabilities of survival and event-free survival of 94% and...
8.
Mantadakis E, Ewalt D, CAVENDER J, Rogers Z, Buchanan G
Blood
. 1999 Dec;
95(1):78-82.
PMID: 10607688
The optimal management of prolonged priapism for patients with sickle cell anemia (SCA) has not been established. We prospectively studied in an outpatient setting the efficacy and safety of a...
9.
Mantadakis E, CAVENDER J, Rogers Z, Ewalt D, Buchanan G
J Pediatr Hematol Oncol
. 1999 Dec;
21(6):518-22.
PMID: 10598664
A questionnaire survey was conducted of patients with homozygous sickle cell anemia (Hb SS) and sickle cell beta(0)-thalassemia (Hb S-beta(0)) between 5 and 20 years of age to determine the...
10.
Sayad A, Farah R, Rogers Z, Heubi J, Buchanan G, Squires Jr R
Clin Pediatr (Phila)
. 1999 Jun;
38(5):293-6.
PMID: 10349527
Hepatic dysfunction occurs commonly in children with sickle cell disease (SCD). Although the etiology is multifactorial, cholestasis is a prominent feature. Serum cholylglycine (CG) has been found to be a...