Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Omolara Risqat Kamson"'
Methylene tetrahydrofolate reductase gene mutation in sickle cell anaemia patients in Lagos, Nigeria
Autor:
Oluwaseun Olabisi Adelekan, Ebele Ifeyinwa Uche, Taiwo Modupe Balogun, Vincent Oluseye Osunkalu, Akinsegun Abduljaleel Akinbami, Kamal Ayobami Ismail, Mulikat Adesola Badiru, Adedoyin Owolabi Dosunmu, Omolara Risqat Kamson
Publikováno v:
The Pan African Medical Journal, Vol 34, Iss 213 (2019)
INTRODUCTION: The significant causes of mortality among individuals with sickle cell anaemia (SCA) such as acute chest syndrome and cerebrovascular disease are related to vascular occlusion. Polymorphisms of the methylene tetrahydrofolate reductase (
Externí odkaz:
https://doaj.org/article/3cfee8b5f1c84a73b91f54c0526fb739
Autor:
Akinsegun Abduljaleel Akinbami, Ebele Ifeyinwa Uche, Aishatu Maude Suleiman, Ann Abiola Ogbena, Festus Olusola Olowoselu, Benjamin Augustine, Mulikat Adesola Badiru, Rafat Abiodun Bamiro, Omolara Risqat Kamson
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 141 (2019)
INTRODUCTION: Sickle cell anaemia (SCA) is an inherited abnormality of haemoglobin associated with reduced life expectancy. Patients' complications include dyslipideamia. This study was aimed at determining the artherogenic index of plasma (AIP) in s
Externí odkaz:
https://doaj.org/article/d2925c6646d34da38c495923fb2378c6
Autor:
Kamal Ismail, Ebele Uche, Esther O. Oluwole, Ann Abiola Ogbenna, Oluwaseun Olabisi Adelekan, Akinsegun Akinbami, Omolara Risqat Kamson, Adedoyin Dosunmu, Mulikat Badiru, V O Osunkalu
Publikováno v:
Journal of Blood Medicine. 10:127-134
Purpose: Hypercoagulability in sickle cell anemia (SCA) may be responsible for the increased development of vascular occlusion in certain organs as well as acute pain episodes. The causes of hypercoagulability in SCA are multifactorial and include ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8077e19817b5fd4a342c8f580c189e10
https://doi.org/10.2147/jbm.s198316
https://doi.org/10.2147/jbm.s198316
Methylene tetrahydrofolate reductase gene mutation in sickle cell anaemia patients in Lagos, Nigeria
Autor:
Akinsegun Akinbami, Taiwo Modupe Balogun, Adedoyin Dosunmu, Oluwaseun Olabisi Adelekan, Mulikat Badiru, Kamal Ismail, Ebele Uche, Omolara Risqat Kamson, V O Osunkalu
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol. 34 No. 1 (2019)
Pan African Medical Journal; Vol. 34 No. 1 (2019)
Introduction:the significant causes of mortality among individuals with sickle cell anaemia (SCA) such as acute chest syndrome and cerebrovascular disease are related to vascular occlusion. Polymorphisms of the methylene tetrahydrofolate reductase (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bac51fdea8a1c3d924bd7296845ca234
https://pubmed.ncbi.nlm.nih.gov/32201547
https://pubmed.ncbi.nlm.nih.gov/32201547
Autor:
Aishatu Maude Suleiman, Mulikat Badiru, Ann Abiola Ogbena, Ebele Uche, Omolara Risqat Kamson, Benjamin Augustine, Rafat Abiodun Bamiro, Akinsegun Akinbami, Festus Olusola Olowoselu
Publikováno v:
The Pan African Medical Journal
Introduction: Sickle cell anaemia (SCA) is an inherited abnormality of haemoglobin associated with reduced life expectancy. Patients' complications include dyslipideamia. This study was aimed at determining the artherogenic index of plasma (AIP) in s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7bf7278064b30edbe4ee75ed707e874
https://doi.org/10.11604/pamj.2019.32.141.17166
https://doi.org/10.11604/pamj.2019.32.141.17166