Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Ifeoma J Emodi"'
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
Publikováno v:
International Journal of Medicine and Health Development, Vol 24, Iss 1, Pp 40-46 (2019)
Background: Human immunodeficiency virus (HIV) infection is a global pandemic. Nigeria has the highest burden of pediatric HIV worldwide. HIV-infected children and their caregivers are predisposed to significant psychosocial disorder. This disorder m
Externí odkaz:
https://doaj.org/article/51ca261b1c0a4e088dd17de88f4ba3ae
Publikováno v:
International Journal of Medicine and Health Development, Vol 21, Iss 1, Pp 5-15 (2016)
Background: The standard case management for acute respiratory infections (ARI) initiated by the World Health Organization (WHO) seeks to reduce pneumonia mortality by encouraging appropriate maternal home-care practices and early treatment from a he
Externí odkaz:
https://doaj.org/article/06a26b87fa9443aa972c019d93759b86
Autor:
Ifeoma J Emodi
Publikováno v:
International Journal of Medicine and Health Development, Vol 8, Iss 2, Pp 27-30 (2003)
First-born twins are at a four-fold risk of acquiring HIV infection if delivered by caesarean section. A female second twin delivered by caesarean section presented at the age of 14 months with features of HIV/AIDS. She died four months later of full
Externí odkaz:
https://doaj.org/article/208bc73357ab46f698b60df00550c5d2
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss 3, Pp 255-260 (2020)
Introduction: Persistent hematuria is a chronic complication of sickle cell anemia (SCA) which can progress to chronic kidney disease. The practice of early detection of persistent hematuria in children with SCA in steady state is important for timel
Externí odkaz:
https://doaj.org/article/75de0c8f26a74cf09f9118b20b43fcf5
Autor:
Anthony N Ikefuna, Uchenna C. Nnajekwu, Osita U Ezenwosu, Ifeoma J Emodi, Chukwubike O. Nnajekwu, Ndubuisi A Uwaezuoke, Vivian O Onukwuli
Publikováno v:
African Health Sciences
Background: Repeated crises in children with sickle cell anaemia (SCA), which is a manifestation of disease severity, results in depletion of their minimal tissue folate stores, with higher likelihood of folate deficiency. The study aimed to determin
Autor:
Uchenna C, Nnajekwu, Chukwubike O, Nnajekwu, Vivian O, Onukwuli, Bartholomew F, Chukwu, Anthony N, Ikefuna, Ifeoma J, Emodi
Publikováno v:
Malawi medical journal : the journal of Medical Association of Malawi. 34(2)
Folic acid supplementation is an integral aspect of the management of children with sickle cell anaemia (SCA) especially in Africa. In spite of this, there have been concerns about lower folate levels, especially during crisis.To determine red cell 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
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss 3, Pp 255-260 (2020)
Hematology, Transfusion and Cell Therapy
Hematology, Transfusion and Cell Therapy, Volume: 42, Issue: 3, Pages: 255-260, Published: 18 SEP 2020
Hematology, Transfusion and Cell Therapy
Hematology, Transfusion and Cell Therapy, Volume: 42, Issue: 3, Pages: 255-260, Published: 18 SEP 2020
Introduction Persistent hematuria is a chronic complication of sickle cell anemia (SCA) which can progress to chronic kidney disease. The practice of early detection of persistent hematuria in children with SCA in steady state is important for timely
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%.