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Swee Lay Thein

Showing results (51-60 of 203) with videos related to

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Expert Review of Hematology|October 3, 2022
Subanesthetic ketamine: the way forward for pain management in sickle cell disease patients?Raissa Nobrega, Veronica Carullo, Swee Lay Thein, et al.
Plos One|December 24, 2019
Neutrophils remain detrimentally active in hydroxyurea-treated patients with sickle cell diseaseEmilia Alina Barbu, Venina M Dominical, Laurel Mendelsohn, et al.
British Journal of Haematology|November 17, 2006
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variationAgeliki Gerovassili, Kypros H Nicolaides, Swee Lay Thein, et al.
Bio-Protocol|March 18, 2021
An Imaging Flow Cytometry Method to Measure Citrullination of H4 Histone as a Read-out for Neutrophil Extracellular Traps FormationEmilia A Barbu, Venina M Dominical, Laurel Mendelsohn, et al.
British Journal of Haematology|October 9, 2003
Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia traitChad Garner, Tracy K Dew, Roy Sherwood, et al.
Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 27, 2016
Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African populationSakina Bibi Loonat, Nitien Hira Naran, Swee Lay Thein, et al.
American Journal of Human Genetics|February 1, 2002
Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobinChad P Garner, Thanusak Tatu, Steve Best, et al.
British Journal of Haematology|October 10, 2012
HbA2 levels in normal adults are influenced by two distinct genetic mechanismsStephan Menzel, Chad Garner, Helen Rooks, et al.
British Journal of Haematology|October 9, 2003
Erythrocytosis and the Chuvash von Hippel-Lindau mutationMelanie J Percy, Michael E J Beard, Chris Carter, et al.
Pageof 21

Showing results (51-60 of 203) with videos related to

Sort By:
Pageof 21
Expert Review of Hematology|October 3, 2022
Subanesthetic ketamine: the way forward for pain management in sickle cell disease patients?Raissa Nobrega, Veronica Carullo, Swee Lay Thein, et al.
Plos One|December 24, 2019
Neutrophils remain detrimentally active in hydroxyurea-treated patients with sickle cell diseaseEmilia Alina Barbu, Venina M Dominical, Laurel Mendelsohn, et al.
British Journal of Haematology|November 17, 2006
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variationAgeliki Gerovassili, Kypros H Nicolaides, Swee Lay Thein, et al.
Bio-Protocol|March 18, 2021
An Imaging Flow Cytometry Method to Measure Citrullination of H4 Histone as a Read-out for Neutrophil Extracellular Traps FormationEmilia A Barbu, Venina M Dominical, Laurel Mendelsohn, et al.
British Journal of Haematology|October 9, 2003
Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia traitChad Garner, Tracy K Dew, Roy Sherwood, et al.
Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 27, 2016
Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African populationSakina Bibi Loonat, Nitien Hira Naran, Swee Lay Thein, et al.
American Journal of Human Genetics|February 1, 2002
Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobinChad P Garner, Thanusak Tatu, Steve Best, et al.
British Journal of Haematology|October 10, 2012
HbA2 levels in normal adults are influenced by two distinct genetic mechanismsStephan Menzel, Chad Garner, Helen Rooks, et al.
British Journal of Haematology|October 9, 2003
Erythrocytosis and the Chuvash von Hippel-Lindau mutationMelanie J Percy, Michael E J Beard, Chris Carter, et al.
Pageof 21