Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Festus Olowoselu"'
Autor:
Ebele Uche, Festus Olowoselu, Benjamin Augustine, Aisha Suleiman, Ayobami Ismail, Esther Oluwole, Akinsegun Akinbami, Lawretta Onwah
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
Externí odkaz:
https://doaj.org/article/f8583dc90c674211bd8cb3bb59a242d8
Autor:
Lakshmanan Krishnamurti, Staci D Arnold, Ann Haight, Allistair Abraham, Gregory MT Guilcher, Tami John, Nitya Bakshi, Shalini Shenoy, Karen Syrjala, Paul L Martin, Sonali Chaudhury, Gretchen Eames, Olusola Festus Olowoselu, Matthew Hsieh, Josu De La Fuente, Kimberly A Kasow, Elizabeth Stenger, Anne Mertens, Fuad El-Rassi, Peter Lane, Bronwen E Shaw, Lillian Meacham, David Archer
Publikováno v:
JMIR Research Protocols, Vol 11, Iss 7, p e36780 (2022)
BackgroundThere are sparse data on the long-term and late effects of hematopoietic cell transplantation (HCT) for sickle cell disease (SCD). ObjectiveThis study aims to establish an international registry of long-term outcomes post-HCT for SCD and d
Externí odkaz:
https://doaj.org/article/30e5d87919a54832b17b351f26b0d417
Autor:
Ebele Uche, Olufunto Kalejaiye, Festus Olowoselu, Timothy Ekwere, Rafatu Bamiro, Abdulateef Kareem, Benjamin Augustine, Odebiyi Hassan, Abdulhafeez Balogun, Akinsegun Akinbami
Publikováno v:
International Journal of Scientific Reports. 9:5-10
Background: In sickle cell anaemia, there is an ever-present risk for haemostatic abnormalities which may result in reduced levels of naturally occurring coagulation inhibitors. Protein S is a Vitamin-K dependent, γ-carboxy glutamic acid-containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed65eb2e4cc146af62384737b39fd840
https://doi.org/10.18203/issn.2454-2156.intjscirep20223370
https://doi.org/10.18203/issn.2454-2156.intjscirep20223370
Autor:
Adegbenga Adetona Ajepe, Kehinde Sharafadeen Okunade, Adebayo Isaiah Sekumade, Ebunoluwa Seun Daramola, Mary Olufunmilayo Beke, Olaolopin Ijasan, Olusola Festus Olowoselu, Bukola Bosede Afolabi
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227965 (2020)
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 (
Externí odkaz:
https://doaj.org/article/569b5de8897341e2894004da0f6b7db0
Autor:
Ifeoma Christiana Udenze, Olusola Festus Olowoselu, Ephraim Uchenna Egbuagha, Temitope Adewunmi Oshodi
Publikováno v:
The Pan African Medical Journal, Vol 26, Iss 52 (2017)
BACKGROUND: the similarities in presentation of cortisol excess, growth hormone deficiency, hypothyroidism and metabolic syndrome suggest that subtle abnormalities of these endocrine hormones may play a causal role in the development of metabolic syn
Externí odkaz:
https://doaj.org/article/99739dbfb88b47d09b70a2bc8a8323db
Autor:
Esther Oluwakemi Oluwole, Chibuike Davidson Okoye, Adedoyin Oyeyimika Ogunyemi, Olusola Festus Olowoselu, Olufemi Abiola Oyedeji
Publikováno v:
The Pan African medical journal. 42
sickle cell disease (SCD) refers to a group of inherited blood disorders that are life-long and affect many people globally. An estimate of 2.3% of the Nigerian population suffer from SCD and about 25% of adults have the sickle cell gene. Premarital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34e9e1c775854393914eec1dd3e94f5e
https://pubmed.ncbi.nlm.nih.gov/35685388
https://pubmed.ncbi.nlm.nih.gov/35685388