Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tolulase A. Olutogun"'
Autor:
Kehinde J. Olufemi-Aworinde, Tolulase A. Olutogun, Joel O. Akande, Roseline O. Akande, Abiona O. Odeyemi, Olufemi J. Idowu, Elizabeth O. Oke, Ademola T. Abolarin, Oluwabukola A. Ala
Publikováno v:
Anemia, Vol 2022 (2022)
Anaemia is a frequent finding in type 2 diabetes, but it is typically seen with established chronic kidney disease and renal insufficiency. Cases, where anaemia predates renal insufficiency, are associated with a worse prognosis for the type 2 diabet
Externí odkaz:
https://doaj.org/article/dd06312d641e4cf3953b3273209ef104
Autor:
Tolulase Aderayo Olutogun, Kehinde Joyce Olufemi-Aworinde, Foluke A Fasola, Gbemi Henry Ano-Edward, Olufemi Opeyemi Aworinde, Anthony O Ajiboye
Publikováno v:
Saudi Journal for Health Sciences, Vol 7, Iss 2, Pp 80-82 (2018)
Background: The homozygous sickle cell anemia (SCA) has an unstable hemoglobin (HbS). The heme group dissociates easily from globin chain and the iron is released and free within the red cell. In addition, the sickle red cells release cell-free hemog
Externí odkaz:
https://doaj.org/article/2a4c9ef9db5c45ef91dcff591399bf83
Autor:
Maria De Angioletti, Lucia Gargiulo, Giovanni Caocci, Annamaria Pellecchia, Tolulase A Olutogun, Rosario Notaro, Margherita Berardi, Giorgio La Nasa, Lucio Luzzatto, Michela Sica
Publikováno v:
Blood 124 (2014).
info:cnr-pdr/source/autori:Sica, Michela; Pellecchia, Annamaria; Berardi, Margherita; Gargiulo, Lucia; Olutogun, Tolulase A.; Caocci, Giovanni; La Nasa, Giorgio; De Angioletti, Maria; Luzzatto, Lucio; Notaro, Rosario/titolo:Complement Activation in Paroxysmal Nocturnal Hemoglobinuria (PNH) Causes Oxidative Damage Which May Affect Response to Eculizumab/doi:/rivista:Blood/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:124
info:cnr-pdr/source/autori:Sica, Michela; Pellecchia, Annamaria; Berardi, Margherita; Gargiulo, Lucia; Olutogun, Tolulase A.; Caocci, Giovanni; La Nasa, Giorgio; De Angioletti, Maria; Luzzatto, Lucio; Notaro, Rosario/titolo:Complement Activation in Paroxysmal Nocturnal Hemoglobinuria (PNH) Causes Oxidative Damage Which May Affect Response to Eculizumab/doi:/rivista:Blood/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:124
PNH is a rare acquired clonal disorder of the hematopoietic stem cell, characterized by a somatic mutation that inactivates the X-linked PIGA gene: this in turn results in deficiency on the cell surface of all proteins anchored by the glycosylphospha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09723b610fb8f30d145c31653a8101c7
http://www.cnr.it/prodotto/i/428374
http://www.cnr.it/prodotto/i/428374
