Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eyiuche D. Ezigbo"'
Autor:
Samsul Anwar, Mudatsir Mudatsir, Youdiil Ophinni, Chika Yamada, Amanda Yufika, Khaoula Aloui, Manel Ferjani, Wajdi Kacem, Rawan Raad, Namareg ME. Khiri, Khan Sharun, Mahir Gachabayov, Lirane ED. Ferreto, María FC. Briones, Marhami Fahriani, Sunil Anandu, Harapan Harapan, Md Ariful Haque, Zeineb Teyeb, Suhrud Panchawagh, Dalia A. Deeb, Dina Emad, Irfan Ullah, Najma I. Malik, Elham Babadi, Edris Kakemam, Abiodun Durosinmi, Esther N. Adejumo, Rocío BI. Morales, Sebastián Lazcano-Díaz, Kirellos Said Abbas, Nasrine Ben Hadj Dahman, Farah S. Sami, Fatma A. Monib, Mohajer IH. Ismaeil, Guilherme W. Wendt, Rashed Y. Adam, Morteza Arab-Zozani, Montacer Hafsi, Asma Y. Ismail, Talha B. Emran, Rashed YA. Abdalla, Daniel M. Felsenreich, Eyiuche D. Ezigbo, Firzan Nainu, Akele R. Yomi, Eva Imelda, Francesco Rosiello, Kuldeep Dhama, Cut Meurah Yeni, Hendrix I. Kusuma, Seyi S. Enitan, Niken Asri Utami, José TO. Aburto, Subramaniam Ramanarayanan, Emmanuel O. Balogun, Jorge ET. Rojas, Milda Husnah
Publikováno v:
F1000Research, Vol 11 (2022)
Background: Risk perceptions of coronavirus disease 2019 (COVID-19) are considered important as they impact community health behaviors. The aim of this study was to determine the perceived risk of infection and death due to COVID-19 and to assess the
Externí odkaz:
https://doaj.org/article/af1c6fde9fa542e89046b6397c0ee9af
Publikováno v:
Thrombosis Update, Vol 1, Iss , Pp 100016- (2020)
Background: The presence of significant bleeding should be distinguishable from non –pathologic bleeding. Bleeding symptoms vary according to sex, age, and ethnicity; in this study, we provide data in an under-reported population. Aims: To assess t
Externí odkaz:
https://doaj.org/article/3c8fbcadca6a409c96e5d1de1b416224
Autor:
Konstantin Strauch, Philipp S. Wild, Anke Adenaeuer, Dagmar Laubert-Reh, Stefano Barco, Eyiuche D Ezigbo, Bernhard Lämmle, Hanan F. Nazir, Karl J. Lackner, Heidi Rossmann, Alice Trinchero
Publikováno v:
Journal of Thrombosis and Haemostasis. 19:147-152
Essentials Prekallikrein (PK) deficiency is a recessive trait with isolated aPTT prolongation. KLKB1 c.451dupT is common in Nigerians (7/600 alleles) and absent in a European group (0/600). To date, all genotyped PK-deficient patients of African ance
Autor:
Anke Adenaeuer, Stefano Barco, Alice Trinchero, Sarah Krutmann, Hanan Fawzy Nazir, Chiara Ambaglio, Vincenzo Rocco, Ylenia Pancione, Luigi Tomao, Arlette Ruiz-Sáez, Marion Echenagucia, Sonja Alesci, Stefanie Sollfrank, Eyiuche D. Ezigbo, Friederike Häuser, Karl J. Lackner, Bernhard Lämmle, Heidi Rossmann
Publikováno v:
Adenaeuer, Anke; Barco, Stefano; Trinchero, Alice; Krutmann, Sarah; Nazir, Hanan Fawzy; Ambaglio, Chiara; Rocco, Vincenzo; Pancione, Ylenia; Tomao, Luigi; Ruiz-Sáez, Arlette; Echenagucia, Marion; Alesci, Sonja; Sollfrank, Stefanie; Ezigbo, Eyiuche D; Häuser, Friederike; Lackner, Karl J; Lämmle, Bernhard; Rossmann, Heidi (2023). Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence. Journal of thrombosis and haemostasis, 21(2), pp. 237-254. Wiley-Blackwell 10.1016/j.jtha.2022.11.011
BACKGROUND Severe high-molecular-weight kininogen (HK) deficiency is a poorly studied autosomal recessive contact system defect caused by pathogenic, biallelic KNG1 variants. AIM We performed the first comprehensive analysis of diagnostic, clinical,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c088ca3ab768b00350dcd0276b83e8e
Autor:
Dott F. Rosiello, Samsul Anwar, Amanda Yufika, Rashed Y. Adam, Mohajer IH. Ismaeil, Asma Y. Ismail, Nesrine BH. Dahman, Montacer Hafsi, Manel Ferjani, Farah S. Sami, Fatma A Monib, Subramaniam R, Sunil Anandu, Md Ariful Haque, Lirane ED. Ferreto, José TO. Aburto, Jorge ET. Rojas, Seyi S. Enitan, Akele R. Yomi, Eyiuche D. Ezigbo, Elham Babadi, Edris Kakemam, Najma I. Malik, Irfan Ullah, Malik Sallam
Publikováno v:
Narra J. 1
Vaccine hesitancy, defined as the reluctance or rejection in receiving a vaccine despite its availability, represents a major challenge to global health efforts aiming to control the ongoing COVID-19 pandemic. Understanding the possible factors corre
Autor:
Afolabi Temitope, Oluwatayo Beatrice Olatundun, Enitan Seyi Samson, Olayanju Ayodeji Olusola, Eyiuche D Ezigbo
Publikováno v:
International Blood Research & Reviews. 8:1-14
Publikováno v:
Journal of Medical Laboratory and Diagnosis. 6:41-47
Von Willebrand factor (VWF) is a complex multimeric, multifunctional glycoprotein. It plays a primary role in haemostasis by forming platelet plugs at sites of vascular injury. The biological breakdown of VWF is mediated by a metalloprotease, ADAMTS-
Publikováno v:
Nigerian Journal of Clinical Practice. 20:235
Background: Polymorphisms in von Willebrand factor (VWF) gene are an important contributor to the expression of VWF gene and differences in ethnic distribution of these single nucleotide polymorphisms (SNPs) exists. Aims: Our objective was to molecul
Autor:
Helen C Okoye, Theresa U Nwagha, Lisa I Eweputanna, Chilota C Efobi, Eyiuche D Ezigbo, Angela O Ugwu, Onochie I Obodo, Charles E Nonyelu
Publikováno v:
International Journal of Medicine and Health Development, Vol 27, Iss 3, Pp 300-305 (2022)
Background: The burden of venous thromboembolism (VTE) can be reduced through awareness programs, as VTE is largely preventable. Objective: We sought to determine the level of knowledge among medical students in Southeast Nigeria. Materials and Metho
Externí odkaz:
https://doaj.org/article/20409e599f084b57b0a05ddec95c7d54