Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment

gan Inusa, Baba P. D., Hsu, Lewis L., Kohli, Neeraj, Patel, Anissa, Ominu-Evbota, Kilali, Anie, Kofi A., Atoyebi, Wale
Cyhoeddwyd yn Int J Neonatal Screen (2019)

Low-dose hydroxycarbamide therapy may offer similar benefit as maximum tolerated dose for children and young adults with sickle cell disease in low-middle-income settings

gan Inusa, Baba Psalm Duniya, Atoyebi, Wale, Hassan, Abdul Aziz, Idhate, Tushar, Dogara, Livingstone, Ijei, Ifeoma, Qin, Yewen, Anie, Kofi, Lawson, Juliana Olufunke, Hsu, Lewis
Cyhoeddwyd yn F1000Res (2018)

Utilising the ‘Getting to Outcomes(®)’ Framework in Community Engagement for Development and Implementation of Sickle Cell Disease Newborn Screening in Kaduna State, Nigeria

gan Inusa, Baba P.D., Anie, Kofi A., Lamont, Andrea, Dogara, Livingstone G., Ojo, Bola, Ijei, Ifeoma, Atoyebi, Wale, Gwani, Larai, Gani, Esther, Hsu, Lewis
Cyhoeddwyd yn Int J Neonatal Screen (2018)

Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic

gan Roy, Noémi B. A., Telfer, Paul, Eleftheriou, Perla, de la Fuente, Josu, Drasar, Emma, Shah, Farrukh, Roberts, David, Atoyebi, Wale, Trompeter, Sara, Layton, D. Mark, Lugthart, Sanne, Stuart‐Smith, Sara, Chakravorty, Subarna, Wright, Josh, Porter, John, Inusa, Baba, Howard, Jo
Cyhoeddwyd yn Br J Haematol (2020)

A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

gan Roy, Noémi B. A., Wilson, Edward A., Henderson, Shirley, Wray, Katherine, Babbs, Christian, Okoli, Steven, Atoyebi, Wale, Mixon, Avery, Cahill, Mary R., Carey, Peter, Cullis, Jonathan, Curtin, Julie, Dreau, Helene, Ferguson, David J. P., Gibson, Brenda, Hall, Georgina, Mason, Joanne, Morgan, Mary, Proven, Melanie, Qureshi, Amrana, Sanchez Garcia, Joaquin, Sirachainan, Nongnuch, Teo, Juliana, Tedgård, Ulf, Higgs, Doug, Roberts, David, Roberts, Irene, Schuh, Anna
Cyhoeddwyd yn Br J Haematol (2016)

Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients

gan Telfer, Paul, de la Fuente, Josu, Sohal, Mamta, Brown, Ralph, Eleftheriou, Perla, Roy, Noémi, Piel, Frédéric B., Chakravorty, Subarna, Gardner, Kate, Velangi, Mark, Drasar, Emma, Shah, Farrukh, Porter, John B., Trompeter, Sara, Atoyebi, Wale, Szydlo, Richard, Anie, Kofi A., Ryan, Kate, Sharif, Joseph, Wright, Josh, Astwood, Emma, Nicolle, C. Sarah, Webster, Amy, Roberts, David J., Lugthart, Sanne, Kaya, Banu, Awogbade, Moji, Rees, David C., Hollingsworth, Rob, Inusa, Baba, Howard, Jo, Layton, D. Mark
Cyhoeddwyd yn Haematologica (2020)