Alsaffar N, Alsaleh M, Alsaleh A, Ghanem N, Al Khamees M, Alqurain M
J Clin Med. 2024; 13(20).
PMID: 39458204
PMC: 11508296.
DOI: 10.3390/jcm13206254.
Kilonzi M, Mlyuka H, Felician F, Mwakawanga D, Chirande L, Myemba D
Hemato. 2024; 2(4):713-726.
PMID: 39211482
PMC: 11361318.
DOI: 10.3390/hemato2040048.
Sasi P, Makubi A, Sangeda R, Ngaeje M, Mmbando B, Soka J
Commun Med (Lond). 2024; 4(1):160.
PMID: 39122788
PMC: 11315961.
DOI: 10.1038/s43856-024-00552-5.
DCosta C, Sharma O, Manna R, Singh M, Singh S, Singh S
Bioeng Transl Med. 2024; 9(4):e10643.
PMID: 39036093
PMC: 11256192.
DOI: 10.1002/btm2.10643.
Namaganda P, Nantume P, Mubiru K, Twimukye A, Wiltshire C
BMC Health Serv Res. 2024; 24(1):666.
PMID: 38802815
PMC: 11131175.
DOI: 10.1186/s12913-024-11125-6.
Use of Disease-Modifying Treatments in Patients With Sickle Cell Disease.
Newman T, Yang J, Suh K, Jonassaint C, Kane-Gill S, Novelli E
JAMA Netw Open. 2023; 6(11):e2344546.
PMID: 37991760
PMC: 10665975.
DOI: 10.1001/jamanetworkopen.2023.44546.
Provider prescription of hydroxyurea in youth and adults with sickle cell disease: A review of prescription barriers and facilitators.
Pizzo A, Porter J, Carroll Y, Burcheri A, Smeltzer M, Beestrum M
Br J Haematol. 2023; 203(5):712-721.
PMID: 37691131
PMC: 11057211.
DOI: 10.1111/bjh.19099.
A feasibility randomized controlled trial of an mHealth app vs booklets for patient-facing guidelines in adults with SCD.
Cronin R, Quaye N, Liu X, Landes K, Crosby L, Kassim A
Blood Adv. 2023; 7(20):6184-6190.
PMID: 37595029
PMC: 10582837.
DOI: 10.1182/bloodadvances.2023010676.
Bidirectional processes linking social determinants of health and pediatric sickle cell anemia management: A qualitative study.
Long K, Blakey A, Amaro C, Eilenberg J, Brochier A, Garg A
Pediatr Blood Cancer. 2023; 70(10):e30539.
PMID: 37470711
PMC: 10619973.
DOI: 10.1002/pbc.30539.
Age-related differences in risks and outcomes of 30-day readmission in adults with sickle cell disease.
Chen M, Ataga K, Hankins J, Zhang M, Gatwood J, Wan J
Ann Hematol. 2023; 102(9):2329-2342.
PMID: 37450055
DOI: 10.1007/s00277-023-05365-5.
Pharmacokinetics and pharmacodynamics of an oral formulation of decitabine and tetrahydrouridine.
Lau H, Woost P, Friedrich U, Clausen W, Jacobberger J, Saunthararajah Y
Eur J Haematol. 2023; 111(3):345-355.
PMID: 37417197
PMC: 10524919.
DOI: 10.1111/ejh.14009.
Knowledge of fertility and perception of fertility treatment among adults with sickle cell disease (KNOW FERTILITY).
Carrithers B, Raja M, Gemmill A, Cayton Vaught K, Christianson M, Lanzkron S
Front Glob Womens Health. 2023; 4:1191064.
PMID: 37360321
PMC: 10287173.
DOI: 10.3389/fgwh.2023.1191064.
Leveraging mathematical modeling to analyze nonadherence for hydroxyurea therapy in sickle cell disease.
Pandey A, Raja R, Estepp J, Ramkrishna D
CPT Pharmacometrics Syst Pharmacol. 2023; 12(6):748-757.
PMID: 37194405
PMC: 10272301.
DOI: 10.1002/psp4.12945.
Psychologists as leaders in equitable science: Applications of antiracism and community participatory strategies in a pediatric behavioral medicine clinical trial.
Williford D, McTate E, Hood A, Reader S, Hildenbrand A, Smith-Whitley K
Am Psychol. 2023; 78(2):107-118.
PMID: 37011163
PMC: 10474572.
DOI: 10.1037/amp0001086.
Hemoglobin and End-Organ Damage in Individuals with Sickle Cell Disease.
Ershler W, De Castro L, Pakbaz Z, Moynahan A, Weycker D, Delea T
Curr Ther Res Clin Exp. 2023; 98:100696.
PMID: 36950457
PMC: 10025127.
DOI: 10.1016/j.curtheres.2023.100696.
Expecting more: the case for incorporating fertility services into comprehensive sickle cell disease care.
Pecker L, Oteng-Ntim E, Nero A, Lanzkron S, Christianson M, Woolford T
Lancet Haematol. 2023; 10(3):e225-e234.
PMID: 36708736
PMC: 10318482.
DOI: 10.1016/S2352-3026(22)00353-2.
Treatment patterns and burden of complications associated with sickle cell disease: A US retrospective claims analysis.
Manwani D, Burnett A, Paulose J, Yen G, Burton T, Anderson A
EJHaem. 2022; 3(4):1135-1144.
PMID: 36467832
PMC: 9713207.
DOI: 10.1002/jha2.575.
Design, Synthesis, and Investigation of Novel Nitric Oxide (NO)-Releasing Aromatic Aldehydes as Drug Candidates for the Treatment of Sickle Cell Disease.
Huang B, Ghatge M, Donkor A, Musayev F, Deshpande T, Al-Awadh M
Molecules. 2022; 27(20).
PMID: 36296435
PMC: 9610770.
DOI: 10.3390/molecules27206835.
Sickle Cell Disease in Children and Adolescents: A Review of the Historical, Clinical, and Public Health Perspective of Sub-Saharan Africa and Beyond.
Egesa W, Nakalema G, Waibi W, Turyasiima M, Amuje E, Kiconco G
Int J Pediatr. 2022; 2022:3885979.
PMID: 36254264
PMC: 9569228.
DOI: 10.1155/2022/3885979.
Surveillance for Sickle Cell Disease - Sickle Cell Data Collection Program, Two States, 2004-2018.
Snyder A, Lakshmanan S, Hulihan M, Paulukonis S, Zhou M, Horiuchi S
MMWR Surveill Summ. 2022; 71(9):1-18.
PMID: 36201430
PMC: 9552568.
DOI: 10.15585/mmwr.ss7109a1.