Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ifeyinwa L. Ezenwosu"'
Autor:
Adah E. Otache, Ifeyinwa L. Ezenwosu, Edmund N. Ossai, Emmanuel A. Nwobi, Stephen O. Abah, Benjamin SC. Uzochukwu
Publikováno v:
BMC Public Health, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Onchocerciasis is a disease of public health concern due to the devastating consequences of the disease which impacts negatively on the lives of the people. The negative impact of the disease may affect its perception and lead to
Externí odkaz:
https://doaj.org/article/1a61dff27198465ab8cd60ca8d9fc2c0
Autor:
Adah E. Otache, Ifeyinwa L. Ezenwosu, Edmund N. Ossai, Elias C. Aniwada, Emmanuel A. Nwobi, Benjamin SC. Uzochukwu
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 16, Iss 2 (2022)
Introduction Onchocerciasis, a neglected tropical disease of public health importance, causes chronic morbidity and severe disability that may impact on health-related quality of life (HRQoL) of the infected people. This study assessed the HRQoL and
Externí odkaz:
https://doaj.org/article/f5d12706951a4671b1efd53e2c994e6b
Publikováno v:
Pakistan BioMedical Journal. :244-251
Unusual microhabitats in different locations present opportunities for the bio-prospecting of actinomycetes with high antimicrobial producing potentials. A total of 113 actinomycetes from specific indigenous microhabitats were isolated and screened f
Autor:
Osita U. Ezenwosu, Barth F. Chukwu, Ndubuisi A. Uwaezuoke, Ifeyinwa L. Ezenwosu, Kelechi O. Urom, Maria I. Udorah, Anthony N. Ikefuna, Ifeoma J. Emodi
Publikováno v:
Pediatric hematology and oncology.
Children with sickle cell anemia (SCA) usually face psychological complications especially depression. Assessment of depression in resource-limited settings may help identify the extent to which the children with SCA in such settings may need its int
Autor:
Anthony N Ikefuna, Echezona E. Ezeanolue, B F Chukwu, Osita U Ezenwosu, Ifeyinwa L Ezenwosu, Ifeoma J Emodi
Publikováno v:
International Journal of Adolescent Medicine and Health. 33:395-400
Objective Our study sought to assesses the knowledge and awareness of individual sickle cell genotype among adolescents. Methods Participants were recruited from a large school in Southeast Nigeria where adult prevalence of sickle cell trait is 25%.
Autor:
Anthony N Ikefuna, Barth F Chukwu, Ifeyinwa L Ezenwosu, Osita U Ezenwosu, Ndubuisi A Uwaezuoke, Ifeoma J Emodi
Publikováno v:
African Health Sciences
Introduction: Glanzmann’s Thrombasthenia (GT) is a rare autosomal recessive bleeding disorder due to defective platelet membrane glycoprotein GP IIb/IIIa (integrin αIIbβ3). The prevalence is estimated at 1:1,000,000 and it is commonly seen in are
Autor:
Adah E. Otache, Ifeyinwa L. Ezenwosu, Edmund N. Ossai, Elias C. Aniwada, Emmanuel A. Nwobi, Benjamin SC. Uzochukwu
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 16, Iss 2, p e0010182 (2022)
PLoS Neglected Tropical Diseases, Vol 16, Iss 2 (2022)
PLoS Neglected Tropical Diseases, Vol 16, Iss 2 (2022)
Introduction Onchocerciasis, a neglected tropical disease of public health importance, causes chronic morbidity and severe disability that may impact on health-related quality of life (HRQoL) of the infected people. This study assessed the HRQoL and
Autor:
Maria Udorah, Chinedu Arthur Idoko, Anthony N Ikefuna, Ifeoma J Emodi, Barth F Chukwu, Ndubuisi A Uwaezuoke, Osita U Ezenwosu, Ifeyinwa L Ezenwosu, Christopher Bismarck Eke
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
Background Sickle cell anaemia (SCA) is the commonest monogenic haematologic disorder resulting from the inheritance of homozygous mutant haemoglobin genes from both parents. Some factors have been identified as important in explaining the variabilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931eae916ef3f506f93c7af297fee01f
https://doi.org/10.21203/rs.3.rs-294737/v1
https://doi.org/10.21203/rs.3.rs-294737/v1
Autor:
Osita U Ezenwosu, Barth F Chukwu, Ikenna K Ndu, Ndubuisi A Uwaezuoke, Ifeyinwa L Ezenwosu, Ifechukwu M Udorah, Anthony N Ikefuna, Ifeoma J Emodi
Publikováno v:
Sahel Medical Journal, Vol 24, Iss 1, Pp 43-47 (2021)
Introduction: Majority of Nigerians are not aware of their personal genotype, and the knowledge about sickle cell disease is quite low. We hypothesize that health education will improve the knowledge and awareness of sickle cell genotype among adoles
Externí odkaz:
https://doaj.org/article/87fdaa8142dc49e794d84e98cc44f089