Sickle Cell Disease.

PubWeight™: 0.89‹?›

🔗 View Article (PMID 28723335)

Published in N Engl J Med on July 20, 2017


Baba Inusa, Joyce Popoola, Ambroise Wonkam

Articles citing this

Sickle Cell Disease. N Engl J Med (2017) 0.75

Articles cited by this

Sickle Cell Disease. N Engl J Med (2017) 4.53

Articles by these authors

Research capacity. Enabling the genomic revolution in Africa. Science (2014) 3.05

Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with sickle cell disease. Blood (2010) 2.15

A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive Events. N Engl J Med (2015) 2.03

Management of neural tube defects in a Sub-Saharan African country: the situation in Yaounde, Cameroon. J Neurol Sci (2008) 1.70

The role of CFTR and SPINK-1 mutations in pancreatic disorders in HIV-positive patients: a case-control study. AIDS (2004) 1.63

The emerging role of T cell Ig mucin 1 in alloimmune responses in an experimental mouse transplant model. J Clin Invest (2008) 1.50

Long-term safety and efficacy of deferasirox (Exjade) for up to 5 years in transfusional iron-overloaded patients with sickle cell disease. Br J Haematol (2011) 1.45

Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure. Blood (2011) 1.37

Frequency and clinical genetics of familial dilated cardiomyopathy in Cape Town: implications for the evaluation of patients with unexplained cardiomyopathy. S Afr Med J (2011) 1.27

Infection in sickle cell disease: a review. Int J Infect Dis (2009) 1.27

Ready to put metadata on the post-2015 development agenda? Linking data publications to responsible innovation and science diplomacy. OMICS (2014) 1.24

Clinical characteristics and outcomes of familial and idiopathic dilated cardiomyopathy in Cape Town: a comparative study of 120 cases followed up over 14 years. S Afr Med J (2011) 1.20

Critical role of donor tissue expression of programmed death ligand-1 in regulating cardiac allograft rejection and vasculopathy. Circulation (2008) 1.16

Human CD4 memory T cells can become CD4+IL-9+ T cells. PLoS One (2010) 1.12

Targeting Tim-1 to overcome resistance to transplantation tolerance mediated by CD8 T17 cells. Proc Natl Acad Sci U S A (2009) 1.06

Factors predicting future ACS episodes in children with sickle cell anemia. Am J Hematol (2014) 0.97

Cytochrome P450 pharmacogenetics in African populations: implications for public health. Expert Opin Drug Metab Toxicol (2014) 0.94

Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa? OMICS (2015) 0.94

Acceptance of abortion by doctors and medical students in Cameroon. Lancet (2007) 0.90

Pandemic influenza A (H1N1) virus infections in children with sickle cell disease. Blood (2010) 0.87

UCT's contribution to medical genetics in Africa - from the past into the future. S Afr Med J (2012) 0.84

Primary stroke prevention in Nigerian children with sickle cell disease (SPIN): challenges of conducting a feasibility trial. Pediatr Blood Cancer (2014) 0.83

In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes. OMICS (2014) 0.83

Rosai-Dorfman disease: a previously unreported association with sickle cell disease. BMC Clin Pathol (2007) 0.83

Biomedical research, a tool to address the health issues that affect African populations. Global Health (2013) 0.83

Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans. OMICS (2014) 0.83

Translating biotechnology to knowledge-based innovation, peace, and development? Deploy a Science Peace Corps--an open letter to world leaders. OMICS (2014) 0.82

Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome. J Community Genet (2012) 0.82

Initiation of prenatal genetic diagnosis of sickle cell anaemia in Cameroon (sub-Saharan Africa). Prenat Diagn (2011) 0.81

A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease. Expert Rev Hematol (2015) 0.80

Silent cerebral infarction, income, and grade retention among students with sickle cell anemia. Am J Hematol (2014) 0.80

Rickets and tracheobronchomalacia. BMJ Case Rep (2009) 0.80

Urethral duplication in a 12-year-old child. Afr J Paediatr Surg (2012) 0.79

Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapy. Am J Hematol (2015) 0.79

Stroke may appear to be rare in Saudi-Arabian and Nigerian children with sickle cell disease, but not in Cameroonian sickle cell patients. Br J Haematol (2006) 0.78

Assessing the quality of life of children with sickle cell anaemia using self-, parent-proxy, and health care professional-proxy reports. Br J Health Psychol (2014) 0.77

Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. Eur J Med Genet (2013) 0.77

Sickle cell anemia: targeting the role of fetal hemoglobin in therapy. Clin Pediatr (Phila) (2007) 0.77

Prenatal diagnosis may represent a point of entry of genetic science in sub-Saharan Africa: a survey on the attitudes of medical students and physicians from Cameroon. Prenat Diagn (2006) 0.77

Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon. Am J Trop Med Hyg (2010) 0.75

A case of familial unilateral tight shoe. Arch Dis Child (2007) 0.75

Hydroxycarbamide use in young children with sickle-cell anaemia. Lancet (2011) 0.75

Problems with implementing a standardised transcranial Doppler screening programme: impact of instrumentation variation on STOP classification. Pediatr Radiol (2011) 0.75

Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype. Hemoglobin (2011) 0.75

Real-time dose adjustment using point-of-care platelet reactivity testing in a double-blind study of prasugrel in children with sickle cell anaemia. Thromb Haemost (2016) 0.75

Appendicular Sinus as a Cause of Chronic Psoas Abscess in a Renal Transplant Recipient: A Case Report. Exp Clin Transplant (2014) 0.75

The measurement of urinary hydroxyurea in sickle cell anaemia. Br J Haematol (2005) 0.75