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Items: 1 to 20 of 101


Enamel defects and tooth eruption disturbances in children with sickle cell anemia.

Lopes CMI, Cavalcanti MC, Alves E Luna AC, Marques KMG, Rodrigues MJ, DE Menezes VA.

Braz Oral Res. 2018 Aug 13;32:e87. doi: 10.1590/1807-3107bor-2018.vol32.0087.


Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters.

Yahouédéhou SCMA, Carvalho MOS, Oliveira RM, Santiago RP, da Guarda CC, Carvalho SP, Ferreira JRD, Aleluia MM, Adorno EV, Gonçalves MS.

Dis Markers. 2018 Jan 28;2018:6105691. doi: 10.1155/2018/6105691. eCollection 2018.


Blood rheological abnormalities in sickle cell anemia.

Connes P, Renoux C, Romana M, Abkarian M, Joly P, Martin C, Hardy-Dessources MD, Ballas SK.

Clin Hemorheol Microcirc. 2018;68(2-3):165-172. doi: 10.3233/CH-189005.


Coexistent sickle-cell anemia and autoimmune disease in eight children: pitfalls and challenges.

Li-Thiao-Te V, Uettwiller F, Quartier P, Lacaille F, Bader-Meunier B, Brousse V, de Montalembert M.

Pediatr Rheumatol Online J. 2018 Jan 17;16(1):5. doi: 10.1186/s12969-017-0221-x.


Effectiveness, safety, and cost of partial exchange transfusions in patients with sickle-cell anemia at a sickle cell disease center in sub-Saharan Africa.

Boma Muteb P, Kaluila Mamba JFJ, Muhau Pfutila P, Bilo V, Panda Mulefu JD, Diallo DA.

Med Sante Trop. 2017 Nov 1;27(4):387-391. doi: 10.1684/mst.2017.0719.


Relationship between zinc levels and anthropometric indices among school-aged female children with sickle cell anemia in enugu, Nigeria.

Onukwuli VO, Ikefuna AN, Nwokocha AR, Emodi IJ, Eke CB.

Niger J Clin Pract. 2017 Nov;20(11):1461-1467. doi: 10.4103/njcp.njcp_104_17.


Assessment of biochemical liver function tests in relation to age among steady state sickle cell anemia patients.

Akuyam SA, Abubakar A, Lawal N, Yusuf R, Aminu SM, Hassan A, Musa A, Bello AK, Yahaya IA, Okafor PA.

Niger J Clin Pract. 2017 Nov;20(11):1428-1433. doi: 10.4103/njcp.njcp_14_17.


Sickle cell retinopathy and other chronic complications of sickle cell anemia: A clinical study of 84 Sub-Saharan African cases (Cameroon).

Bilong Y, Dubert M, Koki G, Noubiap JJ, Pangetna HN, Menet A, Chelo D, Offredo L, Jacob S, Belinga S, Yanda ANA, Kingue S, Jouven X, Ranque B, Bella LA.

J Fr Ophtalmol. 2018 Jan;41(1):50-56. doi: 10.1016/j.jfo.2017.07.005. Epub 2017 Dec 30.


Respiratory resistance and reactance in adults with sickle cell anemia: Correlation with functional exercise capacity and diagnostic use.

Marinho CL, Maioli MCP, do Amaral JLM, Lopes AJ, Melo PL.

PLoS One. 2017 Dec 8;12(12):e0187833. doi: 10.1371/journal.pone.0187833. eCollection 2017.


Perinatal Maternal Mortality in Sickle Cell Anemia: Two Case Reports and Review of the Literature.

Rizk S, Pulte ED, Axelrod D, Ballas SK.

Hemoglobin. 2017 Jul - Nov;41(4-6):225-229. doi: 10.1080/03630269.2017.1397017. Epub 2017 Nov 28. Review.


Gene Addition Strategies for β-Thalassemia and Sickle Cell Anemia.

Dong AC, Rivella S.

Adv Exp Med Biol. 2017;1013:155-176. doi: 10.1007/978-1-4939-7299-9_6. Review.


Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia.

Bernaudin F, Pondarré C, Galambrun C, Thuret I.

Adv Exp Med Biol. 2017;1013:89-122. doi: 10.1007/978-1-4939-7299-9_4.


Novel use Of Hydroxyurea in an African Region with Malaria (NOHARM): a trial for children with sickle cell anemia.

Opoka RO, Ndugwa CM, Latham TS, Lane A, Hume HA, Kasirye P, Hodges JS, Ware RE, John CC.

Blood. 2017 Dec 14;130(24):2585-2593. doi: 10.1182/blood-2017-06-788935. Epub 2017 Oct 19.


A deep convolutional neural network for classification of red blood cells in sickle cell anemia.

Xu M, Papageorgiou DP, Abidi SZ, Dao M, Zhao H, Karniadakis GE.

PLoS Comput Biol. 2017 Oct 19;13(10):e1005746. doi: 10.1371/journal.pcbi.1005746. eCollection 2017 Oct.


Adverse effect of hydroxyurea on spermatogenesis in patients with sickle cell anemia after 6 months of treatment.

Berthaut I, Bachir D, Kotti S, Chalas C, Stankovic K, Eustache F, Ravel C, Habibi A, Brailly-Tabard S, Lévy-Dutel L, Bleibtreu A, Simon T, Galactéros F, Lionnet F, Mandelbaum J.

Blood. 2017 Nov 23;130(21):2354-2356. doi: 10.1182/blood-2017-03-771857. Epub 2017 Sep 28. No abstract available.


Substituting Sodium Hydrosulfite with Sodium Metabisulfite Improves Long-Term Stability of a Distributable Paper-Based Test Kit for Point-of-Care Screening for Sickle Cell Anemia.

Torabian K, Lezzar D, Piety NZ, George A, Shevkoplyas SS.

Biosensors (Basel). 2017 Sep 20;7(3). pii: E39. doi: 10.3390/bios7030039.


A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy.

Estepp JH, Smeltzer MP, Kang G, Li C, Wang WC, Abrams C, Aygun B, Ware RE, Nottage K, Hankins JS.

Am J Hematol. 2017 Dec;92(12):1333-1339. doi: 10.1002/ajh.24906. Epub 2017 Sep 28.


Comparison of Outcomes in Patients Having Acute Myocardial Infarction With Versus Without Sickle-Cell Anemia.

Ogunbayo GO, Misumida N, Olorunfemi O, Elbadawi A, Saheed D, Messerli A, Elayi CS, Smyth SS.

Am J Cardiol. 2017 Nov 15;120(10):1768-1771. doi: 10.1016/j.amjcard.2017.07.108. Epub 2017 Aug 8.


Associations between endothelial dysfunction and clinical and laboratory parameters in children and adolescents with sickle cell anemia.

Teixeira RS, Terse-Ramos R, Ferreira TA, Machado VR, Perdiz MI, Lyra IM, Nascimento VL, Boa-Sorte N, Andrade BB, Ladeia AM.

PLoS One. 2017 Sep 1;12(9):e0184076. doi: 10.1371/journal.pone.0184076. eCollection 2017.

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