Autosomal recessive polycystic kidney disease (ARPKD) in a Nigerian newborn: a case report

por Bolaji, Olufunke, Erinomo, Olagoke, Adebara, Olufunmilayo, Okolugbo, Julia, Onumajuru, Bartholomew, Akanni, Taiwo, Adebami, Olusegun
Publicado 2018

Strengthening retinopathy of prematurity screening and treatment services in Nigeria: a case study of activities, challenges and outcomes 2017-2020

por Ademola-Popoola, Dupe S, Fajolu, Iretiola B, Gilbert, Clare, Olusanya, Bolutife A, Onakpoya, Oluwatoyin H, Ezisi, Chinyelu N, Musa, Kareem O, Chan, Robison Vernon Paul, Okeigbemen, Valentina W, Muhammad, Rilwan C, Malik, Aeesha N J, Adio, Adedayo O, Bodunde, Olubunmi T, Rafindadi, Abdulkadir L, Oluleye, Tunji S, Tongo, Olukemi O, Badmus, Sarat A, Adebara, Olufunmilayo V, Padhi, Tapas Ranjan, Ezenwa, Beatrice N, Obajolowo, Tokunbo S, Olokoba, Lateefat B, Olatunji, Victoria A, Babalola, Yewande Olubunmi, Ugalahi, Mary O, Adenekan, Adetunji, Adesiyun, Omotayo O, Sahoo, Jagdish, Miller, Marilyn T, Uhumwangho, Odarosa M, Olagbenro, Adeduntan S, Adejuyigbe, Ebunoluwa A, Ezeaka, Chinyere V C, Mokuolu, Olugbenga, Ogunlesi, Tinuade A, Ogunfowora, Olusoga B, Abdulkadir, Isa, Abdullahi, Fatima L, Fabiyi, Abosede T, Hassan, Laila H L, Baiyeroju, Aderonke M, Opara, Peace I, Oladigbolu, Kehinde, Eneh, Augusta U, Fiebai, Bassey E, Mahmud-Ajeigbe, Fatima A, Peter, Elijah N, Abdullahi, Hawwa S
Publicado 2021