Athman L, Jonathan A, Musa F, Kipasika H, Mahawi I, Urio F
BMC Pediatr. 2025; 25(1):10.
PMID: 39773631
PMC: 11705873.
DOI: 10.1186/s12887-024-05359-w.
Allison R, Welby E, Ehlers V, Burand A, Isaeva O, Nieves Torres D
Blood. 2024; 143(20):2037-2052.
PMID: 38427938
PMC: 11143522.
DOI: 10.1182/blood.2023022591.
Bawany M, Motov S
Clin Exp Emerg Med. 2022; 9(3):169-175.
PMID: 36168777
PMC: 9561194.
DOI: 10.15441/ceem.22.326.
Kenney M, Smith W
J Pain Res. 2022; 15:879-894.
PMID: 35386424
PMC: 8979590.
DOI: 10.2147/JPR.S343069.
Amaeshi L, Kalejaiye O, Ogamba C, Adelekan Popoola F, Adelabu Y, Ikwuegbuenyi C
Cureus. 2022; 14(1):e21377.
PMID: 35198289
PMC: 8854203.
DOI: 10.7759/cureus.21377.
Identifying elevated risk for future pain crises in sickle-cell disease using photoplethysmogram patterns measured during sleep: A machine learning approach.
Ji Y, Chalacheva P, Rosen C, DeBaun M, Coates T, Khoo M
Front Digit Health. 2021; 3.
PMID: 34396363
PMC: 8360353.
DOI: 10.3389/fdgth.2021.714741.
Mechanisms of pain in sickle cell disease.
Takaoka K, Cyril A, Jinesh S, Radhakrishnan R
Br J Pain. 2021; 15(2):213-220.
PMID: 34055342
PMC: 8138616.
DOI: 10.1177/2049463720920682.
Counselling Needs of Sickle-Cell Anaemia Adolescents in Ekiti State, Nigeria.
Adegboyega L
Ethiop J Health Sci. 2021; 30(6):1005-1010.
PMID: 33883846
PMC: 8047247.
DOI: 10.4314/ejhs.v30i6.19.
Impact of oral -arginine supplementation on blood pressure dynamics in children with severe sickle cell vaso-occlusive crisis.
Onalo R, Cilliers A, Cooper P
Am J Cardiovasc Dis. 2021; 11(1):136-147.
PMID: 33815929
PMC: 8012291.
What is the future of patient-reported outcomes in sickle-cell disease?.
Singh S, Bakshi N, Mahajan P, Morris C
Expert Rev Hematol. 2020; 13(11):1165-1173.
PMID: 33034214
PMC: 7722233.
DOI: 10.1080/17474086.2020.1830370.
How I Treat Acute and Persistent Sickle Cell Pain.
Ballas S
Mediterr J Hematol Infect Dis. 2020; 12(1):e2020064.
PMID: 32952975
PMC: 7485466.
DOI: 10.4084/MJHID.2020.064.
Impact of neuropathic pain on quality of life in adults with sickle cell disease: observational study.
Santos L, Guimaraes M, Baptista A, Sa K
Hematol Transfus Cell Ther. 2020; 43(3):263-267.
PMID: 32576453
PMC: 8446234.
DOI: 10.1016/j.htct.2020.03.010.
S100B single nucleotide polymorphisms exhibit sex-specific associations with chronic pain in sickle cell disease in a largely African-American cohort.
Jhun E, Sadhu N, He Y, Yao Y, Wilkie D, Molokie R
PLoS One. 2020; 15(5):e0232721.
PMID: 32379790
PMC: 7205279.
DOI: 10.1371/journal.pone.0232721.
Phenylethanolamine -methyltransferase gene polymorphisms associate with crisis pain in sickle cell disease patients.
Sadhu N, Jhun E, Posen A, Yao Y, He Y, Molokie R
Pharmacogenomics. 2020; 21(4):269-278.
PMID: 32162598
PMC: 7202258.
DOI: 10.2217/pgs-2019-0096.
Transcutaneous electrical nerve stimulation (TENS) for pain management in sickle cell disease.
Pal S, Dixit R, Moe S, Godinho M, Abas A, Ballas S
Cochrane Database Syst Rev. 2020; 3:CD012762.
PMID: 32124977
PMC: 7059961.
DOI: 10.1002/14651858.CD012762.pub2.
Not being heard: barriers to high quality unplanned hospital care during young people's transition to adult services - evidence from 'this sickle cell life' research.
Renedo A, Miles S, Chakravorty S, Leigh A, Telfer P, Warner J
BMC Health Serv Res. 2019; 19(1):876.
PMID: 31752858
PMC: 6873494.
DOI: 10.1186/s12913-019-4726-5.
Pharmacological interventions for painful sickle cell vaso-occlusive crises in adults.
Cooper T, Hambleton I, Ballas S, Johnston B, Wiffen P
Cochrane Database Syst Rev. 2019; 2019(11).
PMID: 31742673
PMC: 6863096.
DOI: 10.1002/14651858.CD012187.pub2.
CE: Understanding the Complications of Sickle Cell Disease.
Tanabe P, Spratling R, Smith D, Grissom P, Hulihan M
Am J Nurs. 2019; 119(6):26-35.
PMID: 31135428
PMC: 6674980.
DOI: 10.1097/01.NAJ.0000559779.40570.2c.
Chronic pain in adults with sickle cell disease is associated with alterations in functional connectivity of the brain.
Karafin M, Chen G, Wandersee N, Brandow A, Hurley R, Simpson P
PLoS One. 2019; 14(5):e0216994.
PMID: 31107926
PMC: 6527293.
DOI: 10.1371/journal.pone.0216994.
Normal saline bolus use in pediatric emergency departments is associated with poorer pain control in children with sickle cell anemia and vaso-occlusive pain.
Carden M, Brousseau D, Ahmad F, Bennett J, Bhatt S, Bogie A
Am J Hematol. 2019; 94(6):689-696.
PMID: 30916794
PMC: 6510594.
DOI: 10.1002/ajh.25471.