Literature DB >> 3533181

Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.

M H Steinberg, S H Embury.   

Abstract

Recent advances in molecular genetics have permitted detailed study of the human alpha-globin genes and the causes of alpha-thalassemia. In this review, we examine the causes of alpha-thalassemia in the black population and the consequences of the interactions between alpha-thalassemia and structural hemoglobin variants.

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Year:  1986        PMID： 3533181

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


  37 in total

Review 1.  Genetic modifiers of sickle cell disease.

Authors:  Martin H Steinberg; Paola Sebastiani
Journal:  Am J Hematol       Date:  2012-05-28       Impact factor: 10.047

2.  Effect of red blood cell variants on childhood malaria in Mali: a prospective cohort study.

Authors:  Tatiana M Lopera-Mesa; Saibou Doumbia; Drissa Konaté; Jennifer M Anderson; Mory Doumbouya; Abdoul S Keita; Seidina A S Diakité; Karim Traoré; Michael A Krause; Ababacar Diouf; Samuel E Moretz; Gregory S Tullo; Kazutoyo Miura; Wenjuan Gu; Michael P Fay; Steve M Taylor; Carole A Long; Mahamadou Diakité; Rick M Fairhurst
Journal:  Lancet Haematol       Date:  2015-03-24       Impact factor: 18.959

3.  Thirty-year risk of ischemic stroke in individuals with sickle cell trait and modification by chronic kidney disease: The atherosclerosis risk in communities (ARIC) study.

Authors:  Melissa C Caughey; Vimal K Derebail; Nigel S Key; Alexander P Reiner; Rebecca F Gottesman; Abhijit V Kshirsagar; Gerardo Heiss
Journal:  Am J Hematol       Date:  2019-09-10       Impact factor: 10.047

Review 4.  The current state of sickle cell trait: implications for reproductive and genetic counseling.

Authors:  Lydia H Pecker; Rakhi P Naik
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

Review 5.  The current state of sickle cell trait: implications for reproductive and genetic counseling.

Authors:  Lydia H Pecker; Rakhi P Naik
Journal:  Blood       Date:  2018-11-29       Impact factor: 22.113

6.  Can Trimodal Distribution of HbS Levels in Sickle Cell Traits Be Used To Predict the Associated Alpha-Thalassemia For Screening Cases in Central India?

Authors:  B M Warpe; A V Shrikhande; S V Poflee
Journal:  Iran J Pathol       Date:  2016

7.  Hydroxyurea in Sickle Cell Disease: Our Experience in Western India.

Authors:  S V Deshpande; S S Bhatwadekar; Parth Desai; Tarang Bhavsar; Ankit Patel; Amey Koranne; Arpan Mehta; Shweta Khadse
Journal:  Indian J Hematol Blood Transfus       Date:  2015-05-16       Impact factor: 0.900

Review 8.  Negative health implications of sickle cell trait in high income countries: from the football field to the laboratory.

Authors:  Nigel S Key; Philippe Connes; Vimal K Derebail
Journal:  Br J Haematol       Date:  2015-03-07       Impact factor: 6.998

Review 9.  Knowledge insufficient: the management of haemoglobin SC disease.

Authors:  Lydia H Pecker; Beverly A Schaefer; Lori Luchtman-Jones
Journal:  Br J Haematol       Date:  2016-12-16       Impact factor: 6.998

10.  Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.

Authors:  Deepika S Darbari; Mehdi Nouraie; James G Taylor; Carlo Brugnara; Oswaldo Castro; Samir K Ballas
Journal:  Eur J Haematol       Date:  2014-01-30       Impact factor: 2.997
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