Last Updated: May 19, 2016
- We’ve known for 50 years what causes sickle cell disease. Where’s the cure?
Stat News, May 2016 - From Individualized Treatment of Sickle Cell Pain to Precision Medicine: A 40-Year Journey.
Ballas Samir K et al. Journal of clinical medicine research 2016 May (5) 357-60 - Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.
Gaspardi Ane C, et al. Blood transfusion = Trasfusione del sangue 2016 4 1-6 - The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals.
Keyhani Elaheh, et al. Hemoglobin 2016 6 (3) 198-201 - Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana.
Anie Kofi A et al. Journal of community genetics 2016 Apr - Parents' Experiences of Receiving the Initial Positive Newborn Screening (NBS) Result for Cystic Fibrosis and Sickle Cell Disease.
Chudleigh Jane et al. Journal of genetic counseling 2016 Apr - Effect of Hereditary Hemochromatosis Gene (HFE) H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients.
Terzi Yunus Kas?m, et al. Turkish journal of haematology : official journal of Turkish Society of Haematology 2016 4 - Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.
Couque Nathalie et al. British journal of haematology 2016 Apr - Sickle Cell Disease in Central India: A Potentially Severe Syndrome.
Jain Dipty, et al. Indian journal of pediatrics 2016 4 - Hemoglobinopathies in newborns in the southern region of the Triângulo Mineiro, Brazil. Cross-sectional study.
Carlos Aline Menezes et al. Sa~o Paulo medical journal = Revista paulista de medicina 133(5) 439-44 - Newborn screening for sickle cell diseases in the United States: A review of data spanning 2 decades.
Therrell Bradford L et al. Seminars in perinatology 2015 Apr 39(3) 238-51 - Low-complexity biotechnology and everyday aspects of "care:" neonatal testing and sickle cell diagnosis in Brazil.
Calvo-González Elena et al. Historia, ciencias, saude--Manguinhos 2016 Mar 23(1) 79-94 - Key Findings: Sickle Cell Disease in California and Georgia: New Death Rate Estimates
- Sickle-Cell Disease in Nigerian Children: Parental Knowledge and Laboratory Results.
Obaro Stephen K et al. Public health genomics 2016 Mar - Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients.
Zachariah Mathew, et al. Mediterranean journal of hematology and infectious diseases 2016 0 (1) e2016013 - Toward understanding family-related characteristics of young adults with sickle-cell disease or sickle-cell trait in the USA.
Hershberger Patricia E et al. Journal of clinical nursing 2016 Mar - A Cost-Effectiveness Analysis of a Pilot Neonatal Screening Program for Sickle Cell Anemia in the Republic of Angola.
McGann Patrick T et al. The Journal of pediatrics 2015 Dec 167(6) 1314-9 - Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008.
Paulukonis Susan T et al. Public health reports (Washington, D.C. : 1974) 131(2) 367-75 - Cross-Sectional Analysis of Neurocognitive Function, Retinopathy, and Retinal Thinning by Spectral-Domain Optical Coherence Tomography in Sickle Cell Patients.
Oltra Erica Z, et al. Middle East African journal of ophthalmology 0 0 (1) 79-83 - Health literacy and disease-specific knowledge of caregivers for children with sickle cell disease.
Carden Marcus A et al. Pediatric hematology and oncology 2016 Mar 1-13 - Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
Hussein Norita et al. The Cochrane database of systematic reviews 2015 8CD010849 - French guidelines for the management of adult sickle cell disease: 2015 update.
Published on 2015 by Centre de reference maladies rares (syndromes drepanocytaires majeurs) - Association between Duffy antigen receptor expression and disease severity in sickle cell disease patients.
Farawela Hala M, et al. Hematology (Amsterdam, Netherlands) 2016 2 - Screening for Structural Hemoglobin Variants in Bahia, Brazil.
Silva Wellington Santos, et al. International journal of environmental research and public health 2016 0 (2) - Endothelial nitric oxide synthase gene polymorphisms and the risk of vasculopathy in sickle cell disease.
Yousry Sherif M, et al. Hematology (Amsterdam, Netherlands) 2016 2 - Evaluation of a neonatal screening program for sickle-cell disease.
Eller Rodrigo et al. Jornal de pediatria 2016 Feb - Newborn Screening for Sickle Cell Disease: Jamaican Experience.
Mason K et al. The West Indian medical journal 2015 Sep 65(1) - Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/?-thalassemia patients.
Chalikiopoulou Constantina, et al. Pharmacogenomics 2016 2 - Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.
Fong Cristian, et al. Biome?dica : revista del Instituto Nacional de Salud 2015 9 (3) 437-43 - Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.
Upadhye Dipti S, et al. PloS one 2016 0 (1) e0147081
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