Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Adesiyun, O. A."'
Autor:
Abdur-Rahman, Lukman, Raji, T, Lawal, Abdulwahab, Nasir, Abdulrasheed, Adesiyun, O, Abdulkadir, Mohammed, Sayomi, Olayinka, Ayinmode, Iyehunwa, Oyinloye, I, Bolaji, B, Adegboye, K, Adegboye, M, Adeoye, P, Oyedepo, Olanrewaju, Olafimihan, Bola, Olatunbosun, Luqman, Shittu, Akeem, Arinpe, Salahudeen, Deborah, Alonge, Zainab, Rufai
Publikováno v:
Journal of Clinical Sciences; Oct-Dec2023, Vol. 20 Issue 4, p135-140, 6p
Akademický článek
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Autor:
Oyinloye, O. I.1 oyinbuk2001@yahoo.com, Adesiyun, O. A. M.1, Atobatele, M. O.1, Fawole, A. A.1,2
Publikováno v:
Annals of African Medicine. Sep2014, Vol. 13 Issue 3, p138-141. 4p. 2 Black and White Photographs.
Autor:
Adeniji, K. A., Adesiyun, O. A., Nasir, A. A., Abdulmajeed, A. A., Ololu-Zabair, H. T., Oyinloye, A. A., Ayinde, A. A.
Publikováno v:
East African Medical Journal; Vol 93, No 6 (2016); 255-257
Multicystic dysplastic kidney (MCDK) is a congenital, non-heritable maldevelopment in which the renal cortex is replaced by numerous cysts of varying sizes. Typically, MCDK is a unilateral disorder in 76% of cases and bilateral in 24%. The latter is
Publikováno v:
Europe PubMed Central
The Neonatal Intensive Care Unit (NICU) of our hospital has a 30% survival rate among babies born premature weighing1,000g. This hospital serves about 10 million people; there was no retinopathy of prematurity (ROP) screening program in place in Nige
Autor:
Adedoyin, OT, Ibrahim, M, Johnson, WBR, Ojuawo, AO, Mokuolu, OA, Ernest, SK, Adesiyun, O, Adegboye, AO, Akanbi II, AA, Odimayo, S, Adebara, OV, Saka, AO
Publikováno v:
Tropical Journal of Health Sciences; Vol 20, No 1 (2013); 31-36
No Abstract.
Publikováno v:
Case Reports in Urology.
Duplex collecting system is a congenital genitourinary anomaly commonly found incidentally. Our experience with a duplex system associated with giant hydroureter presenting as mobile abdominal swelling that was noticed from birth, constipation, and f
Publikováno v:
SAMJ: South African Medical Journal, Volume: 99, Issue: 5, Pages: 313-313, Published: MAY 2009
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1575::75a512b3b719bb81416de6ca3d7aad73
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742009000500016&lng=en&tlng=en
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742009000500016&lng=en&tlng=en
Publikováno v:
African Journal of Paediatric Surgery; Vol 2, No 1 (2005); 35-36
A case of spontaneous neonatal gastric perforation in a preterm baby presenting as an acute abdomen is presented. The challenges faced at diagnosis are highlighted and the literature is reviewed on the topic.Keywords: gastric perforation, neonate Afr
Autor:
Nasir A Abdulraseed, Abdur-Rahman Lukman Olajide, Adeniran James Olaniyi, Ibrahim O O Kashim, Adesiyun O A Morohunfade, Abdulkadir A. Yisau
Publikováno v:
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association
Background/Aim: Enteric duplication (ED) is a rare congenital anomaly that can occur anywhere along the alimentary tract from the mouth , down to the anus and the nearby organs. This uncommon anomaly may be asymptomatic or presents with vague symptom