Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Kofi A. Anie"'
Autor:
Vivian Paintsil, Mwashungi Ally, Hezekiah Isa, Kofi A. Anie, Josephine Mgaya, Malula Nkanyemka, Victoria Nembaware, Yaa Gyamfua Oppong-Mensah, Flora Ndobho, Lulu Chirande, Abel Makubi, Obiageli Nnodu, Ambroise Wonkam, Julie Makani, Kwaku Ohene-Frempong
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Introduction: Sickle Cell Disease (SCD) causes significant morbidity and mortality particularly in sub-Saharan Africa (SSA) where it contributes to early childhood deaths. There is need to standardize treatment guidelines to help improve overall SCD
Externí odkaz:
https://doaj.org/article/eef189073a754243aefe378963934b3e
Autor:
Paul Telfer, Josu de la Fuente, Mamta Sohal, Ralph Brown, Perla Eleftheriou, Noémi Roy, Frédéric B. Piel, Subarna Chakravorty, Kate Gardner, Mark Velangi, Emma Drasar, Farrukh Shah, John B. Porter, Sara Trompeter, Wale Atoyebi, Richard Szydlo, Kofi A. Anie, Kate Ryan, Joseph Sharif, Josh Wright, Emma Astwood, C. Sarah Nicolle, Amy Webster, David J. Roberts, Sanne Lugthart, Banu Kaya, Moji Awogbade, David C. Rees, Rob Hollingsworth, Baba Inusa, Jo Howard, D. Mark Layton
Publikováno v:
Haematologica, Vol 105, Iss 11 (2020)
Externí odkaz:
https://doaj.org/article/6c8eb0ee441b42e3b6284c91f79e18c8
Autor:
Baba P. D. Inusa, Lewis L. Hsu, Neeraj Kohli, Anissa Patel, Kilali Ominu-Evbota, Kofi A. Anie, Wale Atoyebi
Publikováno v:
International Journal of Neonatal Screening, Vol 5, Iss 2, p 20 (2019)
Sickle cell disease (SCD) is a monogenetic disorder due to a single base-pair point mutation in the β-globin gene resulting in the substitution of the amino acid valine for glutamic acid in the β-globin chain. Phenotypic variation in the clinical p
Externí odkaz:
https://doaj.org/article/ee665d2335a34305a728dec41244524c
Autor:
Baba P.D. Inusa, Kofi A. Anie, Andrea Lamont, Livingstone G. Dogara, Bola Ojo, Ifeoma Ijei, Wale Atoyebi, Larai Gwani, Esther Gani, Lewis Hsu
Publikováno v:
International Journal of Neonatal Screening, Vol 4, Iss 4, p 33 (2018)
Background: Sickle Cell Disease (SCD) has been designated by WHO as a public health problem in sub-Saharan Africa, and the development of newborn screening (NBS) is crucial to the reduction of high SCD morbidity and mortality. Strategies from the fie
Externí odkaz:
https://doaj.org/article/3e76c2fb5f4645d7a273ba0e5c14a4c6
Autor:
Marsha J. Treadwell, Kofi A. Anie
Publikováno v:
Hematology/Oncology Clinics of North America. 36:1137-1149
Publikováno v:
Patient Preference and Adherence. 16:1423-1437
Thalassaemia is one of the commonest inherited genetic disorders world-wide with around 25,000 births of the most severely affected transfusion dependent children annually. Patients with transfusion dependent thalassaemia require regular blood transf
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:
Emma Astwood, Josh Wright, Joseph Sharif, Mark Velangi, Amy P. Webster, Paul Telfer, Wale Atoyebi, Noémi B. A. Roy, D. Mark Layton, Banu Kaya, Jo Howard, Sara Trompeter, Mamta Sohal, Moji Awogbade, C. Sarah Nicolle, Kate Ryan, Rob Hollingsworth, Josu de la Fuente, Richard Szydlo, Emma Drasar, Kate Gardner, Baba Inusa, David C. Rees, Farrukh Shah, Subarna Chakravorty, John Porter, Perla Eleftheriou, Sanne Lugthart, Ralph Brown, Kofi A. Anie, Frédéric B. Piel, David J. Roberts
Publikováno v:
Haematologica
Publikováno v:
The Lancet Child & Adolescent Health. 5:7-9
Autor:
Mahmoud U Sani, David Nana Adjei, Gordon Awandare, Vivian Paintsil, Obiageli Nnodu, Jonathan Stiles, Kofi A Anie, Solomon Fiifi Ofori-Acquah, Julie Makani, Edeghonghon Olayemi, Najibah Aliyu Galadanci, Furahini Tluway, Peter Mensah, Joseph Sarfo-Antwi, Henry Nwokobia, Awwal Gambo, Adebola Benjamin, Arafa Salim, Judith A Osae-Larbi, Amma Benneh-Akwasi Kuma, Anita Ghansah, Catherine Segbefia, Solomon F Ofori-Acquah, William Kudzi, Vivian Painstil, Aisha Kuliya-Gwarzo, Adullahi Shehu, Baba Musa, Mahmoud Sani, Najibah Aliyu Galandanci, Alashle Abimiku, Ameh Adeyefa, Obiageli E. Nnodu, Michael Akinsete, Olufunto Kalejaiye, Titilope Adeyemo, Flora Ndobho, Josephine Mgaya, Siana Nkya, Flordeliza Villanueva, Samit Ghosh, Solomon Ofori-Acquah, Ryan Minster
Publikováno v:
BMJ Open, Vol 11, Iss 7 (2021)
BMJ Open
BMJ Open
ObjectivesTo provide lay information about genetics and sickle cell disease (SCD) and to identify and address ethical issues concerning the Sickle Cell Disease Genomics of Africa Network covering autonomy and research decision-making, risk of SCD com