Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Obiageli E Nnodu"'
Autor:
Godwin O Akaba, Obiageli E Nnodu, Nessa Ryan, Emmanuel Peprah, Teddy E Agida, Dilly O C Anumba, Bissallah A Ekele
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0244984 (2021)
BackgroundAddressing the problem of maternal mortality in Nigeria requires proper identification of maternal deaths and their underlying causes in order to focus evidence-based interventions to decrease mortality and avert morbidity.ObjectivesThe obj
Externí odkaz:
https://doaj.org/article/9001d29bdd724005a3bc3c04d7d2c90d
Autor:
Nchangwi Syntia Munung, Victoria Nembaware, Jantina de Vries, Daima Bukini, Furahini Tluway, Marsha Treadwell, Raphael Zozimus Sangeda, Gaston Mazandu, Mario Jonas, Vivian Paintsil, Obiageli E. Nnodu, Emmanuel Balandya, Julie Makani, Ambroise Wonkam
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Sickle cell disease (SCD) is one of the most prevalent genetic conditions in sub-Saharan Africa. It is a chronic, lifelong disease often characterized by severe pain. However, SCD has received little investment terms of health research, though there
Externí odkaz:
https://doaj.org/article/dc59e4cb1a4c408c970ae599fa87826a
Autor:
Godwin O Akaba, Assaf P. Oron, Alayo Sopekan, Dennis L. Chao, Frédéric B. Piel, Obiageli E Nnodu
Publikováno v:
e731
e723
The Lancet. Haematology
e723
The Lancet. Haematology
Summary Background Child mortality from sickle cell disease in sub-Saharan Africa is presumed to be high but is not well quantified. This uncertainty contributes to the neglect of sickle cell disease and delays the prioritisation of interventions. In
Publikováno v:
Frontiers in Genetics. 13
Background: HemoTypeSC is a rapid, point-of-care testing (POCT) device for sickle cell disease (SCD) that traditionally uses the capillary blood from heel stick collected at the point of testing, a procedure that makes mass screening cumbersome and l
Autor:
Nancy S. Green, Andrew Zapfel, Obiageli E. Nnodu, Patience Franklin, Venée N. Tubman, Lulu Chirande, Charles Kiyaga, Catherine Chunda-Liyoka, Bernard Awuonda, Kwaku Ohene-Frempong, Baba P. D. Inusa, Russell E. Ware, Isaac Odame, Emmanuela E. Ambrose, Livingstone G. Dogara, Assaf P. Oron, Chase Willett, Alexis A. Thompson, Nancy Berliner, Theresa L. Coetzer, Enrico M. Novelli
Publikováno v:
Blood advances. 6(24)
Sickle cell disease (SCD) is a common condition within sub-Saharan Africa and associated with high under-5 mortality (U5M). The American Society of Hematology instituted the Consortium on Newborn Screening in Africa (CONSA) for SCD, a 7-country netwo
Autor:
Marco Vincenzo Lenti, Sarah Luu, Rita Carsetti, Faith Osier, Rodney Ogwang, Obiageli E. Nnodu, Ursula Wiedermann, Jo Spencer, Franco Locatelli, Gino Roberto Corazza, Antonio Di Sabatino
Publikováno v:
Nature reviews. Disease primers. 8(1)
Asplenia (the congenital or acquired absence of the spleen) and hyposplenism (defective spleen function) are common causes of morbidity and mortality. The spleen is a secondary lymphoid organ that is responsible for the regulation of immune responses
Autor:
Siana Nkya, Bruno P. Mmbando, Uche Nnebe-Agumadu, Obiageli E Nnodu, Mario Jonas, Emmanuel Peprah, Kwaku Ohene-Frempong, Adekunle Adekile, Hezekiah Isa, Joyce Gyamfi, Alex Osei-Akoto, Arthemon Nguweneza, Emmanuel Balandya, Ambroise Wonkam, Vivian Paintsil, Victoria Nembaware, Andre Pascal Kengne, Anazoeze Jude Madu, Raphael Z. Sangeda, Emile R. Chimusa, S.A. Asala, Chide E Okocha, Biobele J. Brown, Julie Makani
Publikováno v:
Hemoglobin
Sickle cell disease is a genetic disease with a predisposition to infections caused by encapsulated organisms, especially Streptococcus pneumoniae. Pneumococcal vaccines and prophylactic penicillin have reduced the rate of this infection and mortalit
Autor:
Kambe Banda, David N. Adjei, Uzima Chirwa, Obiageli E Nnodu, Assaf P. Oron, Isaac Nyanor, Upendo Masamu, Gaston K. Mazandu, Patience Kuona, Victoria Nembaware, Andre Pascal Kengne, Andrew D. Campbell, Daima Bukini, Jade Hotchkiss, Julie Makani, Nchangwi Syntia Munung, Mario Jonas, Catherine Chunda-Liyoka, Vivian Painstil, Jean-Michel Serufuri, Jill Kent, Kevin K Esoh, Miriam V Flor-Park, Malula Nkanyemka, Deogratias Munube, Ambroise Wonkam, Chandré Oosterwyk, Valentina Josiane Ngo Bitoungui, Annette Uwineza, Bamidele O. Tayo, Arthemon Nguweneza, Khuthala Mnika, Jack Morrice, Nicola Mulder, Nathan Edward Siebu, Kofi A. Anie, Agnes Jonathan
Publikováno v:
OMICS : a Journal of Integrative Biology
Sickle cell disease (SCD) is one of the most common blood disorders impacting planetary health. Over 300,000 newborns are diagnosed with SCD each year globally, with an increasing trend. The sickle cell disease ontology (SCDO) is the most comprehensi
Autor:
Dennis L. Chao, Assaf P. Oron, Guillaume Chabot-Couture, Alayo Sopekan, Uche Nnebe-Agumadu, Imelda Bates, Frédéric B. Piel, Obiageli E. Nnodu
IntroductionAnaemia is a major cause of morbidity and mortality among children in sub-Saharan Africa. Anaemia has many aetiologies best addressed by different treatments, so regional studies of the aetiology of anaemia may be required.MethodsWe analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a6332a7c35e52db02c32a3c0a7047d0
https://doi.org/10.1101/2022.03.23.22272825
https://doi.org/10.1101/2022.03.23.22272825
Autor:
Emmanuel Chide, Okocha, Joyce, Gyamfi, Nessa, Ryan, Oluwatoyin, Babalola, Eno-Abasi, Etuk, Reuben, Chianumba, Maxwell, Nwegbu, Hezekiah, Isa, Anazoeze Jude, Madu, Samuel, Adegoke, Uche, Nnebe-Agumandu, Biobele, Brown, Emmanuel, Peprah, Obiageli E, Nnodu
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Frontiers in Genetics
Frontiers in Genetics
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,