Výsledky vyhledávání - "Okocha Emmanuel Chide"

Akademický článek

Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease.

Autor: Labarque, Veerle^1,2 (AUTHOR) veerle.labarque@uzleuven.be, Okocha, Emmanuel Chide³ (AUTHOR)

Publikováno v: International Journal of Molecular Sciences. May2024, Vol. 25 Issue 10, p5427. 19p.

Zobrazit plný text záznamu

Plný text ve formátu HTML

Akademický článek

Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registry

Autor: Nchangwi Syntia Munung, Victoria Nembaware, Lawrence Osei-Tutu, Marsha Treadwell, Okocha Emmanuel Chide, Daima Bukini, Hilda Tutuba, SickleInAfrica ELSI WG, Ambroise Wonkam

Publikováno v: BMC Medical Ethics, Vol 23, Iss 1, Pp 1-10 (2022)

Abstract The enrolment of children and adolescents in health research requires that attention to be paid to specific assent and consent requirements such as the age range for seeking assent; conditions for parental consent (and waivers); the age grou

Externí odkaz: https://doaj.org/article/860302283f764fe59c60cf93cba63ddc

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Evaluation of the Serum Status of E-Selectin and Its Correlation with Disease Severity among Steady State Patients with Sickle Cell Anaemia

Autor: Ifeoma Clara Ajuba, Ugochi Jane Chilaka, Onah Christian Ejike, Ngozi Immaculata Ugwu, Ekesiobi Chiazokam Benedette, Okocha Emmanuel Chide, Manafa Patrick Onochie

Publikováno v: Journal of Advances in Medicine and Medical Research. :250-257

Introduction: Sickle cell anemia (SCA) is a disease in which hemoglobin S exists in a homozygous state, with prominent clinical features and a wide range of phenotypes. This study aimed to determine the levels of E-selectin and how it correlated with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bc2cd937892a5344be00a1ba72fed57f
https://doi.org/10.9734/jammr/2022/v34i244923

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Barriers to Therapeutic Use of Hydroxyurea for Sickle Cell Disease in Nigeria: A Cross-sectional Survey

Autor: Hezekiah Isa, Maxwell M. Nwegbu, Okocha Emmanuel Chide, Uche Nnebe-Agumandu, Anazoeze Jude Madu, Emmanuel Peprah, Joyce Gyamfi, Babalola Oluwatoyin, Nessa Ryan, Reuben Chianumba, Samuel Ademola Adegoke, Etuk Eno-Abasi, Obiageli E Nnodu

Background: Sickle cell disease, the inherited blood disorder characterized by anemia, severe pain and other vaso-occlusive complications, acute chest syndrome, disproportionate hospitalization, and early mortality, has significant financial, social,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::48c12dfbfa441597c182470ff8977d42
https://doi.org/10.21203/rs.3.rs-33381/v1

Zobrazit plný text záznamu

Akademický článek

Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registry.

Autor: Munung, Nchangwi Syntia, Nembaware, Victoria, Osei-Tutu, Lawrence, Treadwell, Marsha, Chide, Okocha Emmanuel, Bukini, Daima, Tutuba, Hilda, SickleInAfrica ELSI WG, Nkanyemka, Malula, Anie, Kofi, Royale, Charmaine, Wonkam, Ambroise

Publikováno v: BMC Medical Ethics; 12/8/2022, Vol. 23 Issue 1, p1-10, 10p

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání