Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Aneke, JC"'
Autor:
Okocha EC, Aneke JC, Ulasi TO, Ezeudu CE, Umeh EO, Ebubedike UR, Ukah CO, Onwukamuche ME, Anyiam DC, Onyiaorah IV, Ndukwe CO, Ekwunife OH, Ugwu JO
Publikováno v:
Nigerian Journal of Paediatrics, Vol 42, Iss 2, Pp 111-115 (2024)
Background: Cancer remains a major cause of death in children and adolescents, and differs in adults in nature, distribution and prognosis1 . A culture of case documentation is lacking in our environment and many cases go unreported. Study objective
Externí odkaz:
https://doaj.org/article/cb583656f9b5450095056398daa628e9
Publikováno v:
Nigerian Journal of Paediatrics, Vol 42, Iss 2, Pp 142-146 (2024)
Background and Objective: In P. falciparum malaria (PFM) infestation there are marked changes in cytokine production as the body mounts an immune response to it. Hence we set out to study these changes. Methods: A total of 158 cases of PFM among c
Externí odkaz:
https://doaj.org/article/7921635f0a8747ecb2c339c3e47f0c20
Publikováno v:
Nigerian Journal of Paediatrics, Vol 41, Iss 3, Pp 244-246 (2024)
Childhood acute lymphoblastic leukaemia, (ALL) is increasingly reported to present in an atypical fashion which may have significant implications for treatment outcomes and survival. This case report presents a Nigerian child who’s clinical and r
Externí odkaz:
https://doaj.org/article/11b19a1148524d6eaba7a4df9f536fbf
Clinical and Laboratory Features of Nigerian Patients with Chronic Myeloid Leukaemia: A Cohort Study
Introduction: Chronic myeloid leukaemia (CML) is a clonal haematological condition characterized by marked leukocytosis, with preponderance of leucocyte series at different levels of maturation. Bone marrow suppression with symptomatic cytopaenias an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39969e914567f5acd1f1bb7adb51f710
Autor:
PO, Manafa, Okocha EC, O, Ekuma-Okereke, Aneke, JC, Ikegwuonu JA, NC, Ibe, Chukwuanukwu RC, Mbachu NA, KE, Nwene, Ebugosi RS, Manafa VI, Ihim AC
Background of study: Sickle Cell Disease (SCD) is an inherited haemoglobinopathy characterized by life-long haemolytic anaemia and vaso-occlussive crisis. Oxidative stress may be linked to its pathophysiology which may lead to several organ damage an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288909c97e2cdee579e2b5ddff35d0ed
Publikováno v:
Orient Journal of Medicine; Vol 27, No 1-2 (2015); 61-64
Stevens-Johnson syndrome is an adverse muco-cutaneous complication arising from a number of conditions which include the administration of some drugs. A female Nigerian with chronic lymphocytic leukaemia, (Binet stage C) who developed Stevens-Johnson
Publikováno v:
Orient Journal of Medicine; Vol 27, No 1-2 (2015); 34-39
Background: The presence of high titres of haemolysins (lytic antibodies) in the sera of donors could predispose to adverse blood transfusion reactions.Objective: To evaluate the prevalence of haemolysins among blood donors at the Nnamdi Azikiwe Univ
Autor:
Okocha, EC, Aneke, JC, Ulasi, TO, Ezeudu, CE, Umeh, EO, Ebubedike, UR, Ukah, CO, Onwukamuche, ME, Anyiam, DC, Onyiaorah, IV, Ndukwe, CO, Ugwu, JO, Ekwunife, OH
Publikováno v:
Nigerian Journal of Paediatrics; Vol 42, No 2 (2015); 111-115
Background: Cancer remains a major cause of death in children and adolescents, and differs in adults in nature, distribution and prognosis1. A culture of case documentation is lacking in our environment and many cases go unreported.Study objectives:
Publikováno v:
Nigerian Journal of Paediatrics; Vol 42, No 2 (2015); 142-146
Background and Objective: In P. falciparum malaria (PFM) infestation there are marked changes in cytokine production as the body mounts an immune response to it. Hence we set out to study these changes.Methods: A total of 158 cases of PFM among child
Autor:
Aneke, JC, Adegoke, AO, Oyekunle, AA, Osho, PO, Sanusi, AA, Okocha, EC, Okonkwo, KU, Ibeh, NC, Akinola, NO, Durosinmi, MA
Publikováno v:
Orient Journal of Medicine; Vol 26, No 3-4 (2014); 88-93
Background: Sickle cell disease (SCD) has adverse effects on the kidneys which impact on clinical outcome.Objectives: To study and compare some clinical and haematological profiles in SCD patients, with and without chronic kidney disease (CKD).Method