Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Olusola, Olowoselu"'
Autor:
Akinsegun Akinbami, Ola Bola, Ebele Uche, Mulikat Badiru, Olusola Olowoselu, Aishatu Maude Suleiman, Benjamin Augustine
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 94-98 (2019)
BACKGROUND: Prolonged use of pentazocine in sickle cell disease (SCD) because of chronic pain may result in mental dependence (addiction) and/or physical dependence leading to withdrawal symptoms on suddenly stopping its use. This study was aimed at
Externí odkaz:
https://doaj.org/article/4b812653b10e46aa999f69570fdc9978
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
Akademický článek
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Autor:
Antonella Isgrò, Javid Gaziev, Marco Marziali, Katia Paciaroni, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Festus Olusola Olowoselu, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017030-e2017030 (2017)
Children with sickle cell anemia (SCA) are prone to invasive infections caused by S. pneumonia, H. influenzae, and Plasmodium falciparum. The presence of asthma increases the risk of mortality, and it has been shown an association between the presenc
Externí odkaz:
https://doaj.org/article/eece0808eaad4e048ff5c25e18f9fe0e
Autor:
Kehinde S Okunade, Olayemi Olubunmi Dawodu, Omolola Salako, Sarah John-Olabode, Aloy Okechukwu Ugwu, Rose I Anorlu, Muisi A Adenekan, Olusola Olowoselu, Chidinma Magnus Nwogu, O. Awofeso
Publikováno v:
Nigerian journal of clinical practice
Nigerian Journal of Clinical Practice; Vol. 23 No. 8 (2020); 1141-1147
Nigerian Journal of Clinical Practice; Vol. 23 No. 8 (2020); 1141-1147
Aims:This study was aimed at investigating the prognostic impact of pretreatment thrombocytosis in epithelial ovarian cancer (EOC) patients in Lagos, Nigeria.Methods:This was a retrospective cohort study involving the review of the clinical record of
Autor:
Benjamin Augustine, Akinsegun Akinbami, Lawretta Onwah, Aisha Suleiman, Ayobami Ismail, Esther O. Oluwole, Ebele Uche, Festus Olusola Olowoselu
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 2, Pp 59-63 (2020)
INTRODUCTION: Sickle cell anemia is associated with intense oxidative stress, and optimal antioxidant levels are essential to prevent continuous oxidant tissue damage. The role of oxidant damage to red blood cells in sickle cell anemia (SCA) has been
Autor:
Sulaimon Akanmu, Olusanjo E Moses, Aloy Okechukwu Ugwu, Phyllis J. Kanki, Olusola Olowoselu, Rabiu Ka, Muisi A Adenekan, Kehinde S Okunade, Adebola A Adejimi, Adegbenga Ajepe, Oluwatosin J Akinsola, Sarah John-Olabode, Basirat O Hassan, Chidinma Magnus Nwogu
Publikováno v:
Int J Gynaecol Obstet
OBJECTIVE: To examine the effects of selenium supplementation on pregnancy out-comes and disease progression among HIV-infected pregnant women in Lagos. METHODS: A randomized, placebo-controlled trial conducted among HIV-positive pregnant women betwe
Autor:
Adegbenga Ajepe, Adebayo Sekumade, Kehinde S Okunade, Olaolopin Ijasan, Olusola Olowoselu, Bukola Bosede Afolabi, Ebunoluwa Daramola, Mary Olufunmilayo Beke
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227965 (2020)
PLoS ONE
PLoS ONE
Anaemia in pregnancy is a major health problem and an important cause of adverse foetomaternal outcomes in developing countries. Iron deficiency is the cause of the overwhelming majority of the cases of anaemia in pregnancy. Iron deficiency anaemia (
Autor:
Allistair Abraham, Sonali Chaudhury, Peter A. Lane, Kimberly A. Kasow, Matthew M. Hsieh, Gregory M.T. Guilcher, Nitya Bakshi, Kirshma Khemani, Tami John, Festus Olusola Olowoselu, Lillian R. Meacham, Lakshmanan Krishnamurti, Anirudh Veludhandi, Monica Bhatia, Staci D. Arnold
Publikováno v:
Blood. 138:3030-3030
Introduction Recipients of Hematopoietic Cell Transplantation (HCT) are at risk for treatment related late effects including cardiovascular disease and diabetes. Physical fitness including mobility and muscle strength are important predictors of card
Autor:
Benjamin Augustine, Adedoyin Dosunmu, Akinsegun Akinbami, Ebele Uche, Ayobami Ismail, Abdul-Hafeez O. Balogun, Olusola Olowoselu
Publikováno v:
Nigerian Medical Journal : Journal of the Nigeria Medical Association
Background: Sickle cell anaemia is an autosomal recessive disorder which occurs as a result of the substitution of glutamic acid with valine at the 6th position of the haemoglobin beta chain, resulting in the synthesis of abnormal haemoglobin and the