Literature DB >> 11844993

Sickle cell disease in Africa.

Dapa Diallo1, Gil Tchernia.   

Abstract

Africa is the main birthplace of sickle mutations; the number of newborns affected by sickle cell disease is estimated at 200,000 per year. However, because of low family income and public health funding and, to a lesser extent, because of local beliefs about sickle cell disease, overall treatment of patients is still poor and, in some places, inadequate. Efforts to adapt therapeutic options and overcome difficulties are presented and analyzed.

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Year:  2002        PMID: 11844993     DOI: 10.1097/00062752-200203000-00005

Source DB:  PubMed          Journal:  Curr Opin Hematol        ISSN: 1065-6251            Impact factor:   3.284


  37 in total

1.  Primary stroke prevention in Nigerian children with sickle cell disease (SPIN): challenges of conducting a feasibility trial.

Authors:  Najibah A Galadanci; Shehu U Abdullahi; Musa A Tabari; Shehi Abubakar; Raymond Belonwu; Auwal Salihu; Kathleen Neville; Fenella Kirkham; Baba Inusa; Yu Shyr; Sharon Phillips; Adetola A Kassim; Lori C Jordan; Muktar H Aliyu; Brittany V Covert; Michael R DeBaun
Journal:  Pediatr Blood Cancer       Date:  2014-11-14       Impact factor: 3.167

Review 2.  Sickle cell disease in Africa: burden and research priorities.

Authors:  J Makani; T N Williams; K Marsh
Journal:  Ann Trop Med Parasitol       Date:  2007-01

Review 3.  Neurologic complications in children under five years with sickle cell disease.

Authors:  Aisha A Galadanci; Michael R DeBaun; Najibah A Galadanci
Journal:  Neurosci Lett       Date:  2019-04-27       Impact factor: 3.046

4.  Neurological Complications in Subjects With Sickle Cell Disease or Trait: Genetic Results From Mali.

Authors:  Guida Landouré; Lassana Cissé; Boubacar A Touré; Abdoulaye Yalcouyé; Toumany Coulibaly; Mamadou Karambé; Adama S Sissoko; Thomas Coulibaly; Ambroise Wonkam; Cheick O Guinto
Journal:  Glob Heart       Date:  2017-04-01

Review 5.  Emerging point-of-care technologies for sickle cell disease screening and monitoring.

Authors:  Yunus Alapan; Arwa Fraiwan; Erdem Kucukal; M Noman Hasan; Ryan Ung; Myeongseop Kim; Isaac Odame; Jane A Little; Umut A Gurkan
Journal:  Expert Rev Med Devices       Date:  2016-11-22       Impact factor: 3.166

6.  Understanding the roles of intrinsic disorder in subunits of hemoglobin and the disease process of sickle cell anemia.

Authors:  Reis Fitzsimmons; Narmin Amin; Vladimir N Uversky
Journal:  Intrinsically Disord Proteins       Date:  2016-12-21

7.  Malaria in patients with sickle cell anemia: burden, risk factors, and outcome at the outpatient clinic and during hospitalization.

Authors:  Julie Makani; Albert N Komba; Sharon E Cox; Julie Oruo; Khadija Mwamtemi; Jesse Kitundu; Pius Magesa; Stella Rwezaula; Elineema Meda; Josephine Mgaya; Kisali Pallangyo; Emelda Okiro; David Muturi; Charles R Newton; Gregory Fegan; Kevin Marsh; Thomas N Williams
Journal:  Blood       Date:  2009-11-09       Impact factor: 22.113

8.  Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya.

Authors:  Albert N Komba; Julie Makani; Manish Sadarangani; Tolu Ajala-Agbo; James A Berkley; Charles R J C Newton; Kevin Marsh; Thomas N Williams
Journal:  Clin Infect Dis       Date:  2009-07-15       Impact factor: 9.079

9.  An up-date on the prevalence of sickle cell trait in Eastern and Western Uganda.

Authors:  Andrew L Okwi; Wilson Byarugaba; Christopher M Ndugwa; Arthur Parkes; Michael Ocaido; James K Tumwine
Journal:  BMC Blood Disord       Date:  2010-06-23

10.  An observational study of children with sickle cell disease in Kilifi, Kenya.

Authors:  Manish Sadarangani; Julie Makani; Albert N Komba; Tolu Ajala-Agbo; Charles R Newton; Kevin Marsh; Thomas N Williams
Journal:  Br J Haematol       Date:  2009-07-23       Impact factor: 6.998

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