Zobrazeno 1 - 10
of 10
pro vyhledávání: '"A. S. Baduku"'
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Abstract Background Apert syndrome is a rare genetic disease that presents a diagnostic dilemma because of its similarity with other craniosynostosis syndromes. Currently, there is paucity of reports about adult patients in African medical literature
Externí odkaz:
https://doaj.org/article/5d8bd6e150794610afe064f67df41809
Autor:
T S, Baduku
Publikováno v:
Nigerian journal of clinical practice. 24(7)
There has been a slow but steady decline in the frequency of contrast fluoroscopic studies performed all over the world, including oesophagography. This trend is attributed to the increasing availability of endoscopy, computed tomography (CT), and ma
Autor:
Caleb Mohammed, A Mohammed Durosinlorun, Joel A Adze, Matthew C Taingson, Stephen B Bature, S Baduku
Publikováno v:
JOURNAL OF RESEARCH IN BASIC AND CLINICAL SCIENCES. 2
Precocious puberty is the onset of puberty before the age of 8 years in girls and 9 years in boys. There is a global trend towards earlier onset of puberty. The prevalence is not known in Nigeria. Precocious puberty has implications such as inappropr
Autor:
Shuaibu Saidu Musa, Kamaludeen Shehu, Abdullahi Y. Ashiru, Christiana Kantiyok, Abdulkadir Musa Tabari, Hauwa’u Evelyn Yusuf, Tokan S. Baduku, Musa Abubakar Kana, Salamatu Jibrin, Jimoh M. Ibrahim, Halimah Safiyan, Jenifer Ahmed, Henrique Barros, Ashel Dache Sunday, Stephanie J. London
Publikováno v:
Paediatric and Perinatal Epidemiology
Background:Developing countries bear the burden of childhood stunting but lack resources for cohort studies to develop preventive strategies. To enable future prospective studies, we designed and tested the Child Electronic Growth Monitoring System (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0b977b929b4742d6731a77bb14277e9
https://hdl.handle.net/10216/143099
https://hdl.handle.net/10216/143099
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Background Apert syndrome is a rare genetic disease that presents a diagnostic dilemma because of its similarity with other craniosynostosis syndromes. Currently, there is paucity of reports about adult patients in African medical literature. Therefo
Publikováno v:
Journal of Radiation Medicine in the Tropics. 1:79
Background: Seizures are intracranial neuronal disorders that are observed globally but often poorly investigated and managed in developing countries. The advent of modern diagnostic tools, such as computed tomography (CT) and magnetic resonance imag
Publikováno v:
Archives of International Surgery. 9:67
Background: Head injuries are common causes of morbidity and mortality in trauma patients. Computed tomography (CT) is an important imaging modality in the management of patients with a head injury. This study aimed at documenting the pattern of CT f
Autor:
Farman B Isah, Tokan S. Baduku
Publikováno v:
Archives of International Surgery. 9:16
Sinonasal phycomycosis or zygomycosis is an opportunistic infection caused by mold fungi belonging to the class Zygomycetes. These fungi are widely distributed in nature and mainly infect immunosuppressed patients. Herein, we present the rare case of
Publikováno v:
Community Mental Health Journal. 45:19-25
We report a prospective follow-up of 81 patients recently discharged from the hospital. Their hospital attendance pattern, medication compliance, mental state and social functioning were measured. Defaulters were followed up in the community. At 3 mo
Publikováno v:
Archives of International Surgery. 5:184
Mucoepidermoid carcinoma (MEC) of the sinonasal area is very rare and frequently misclassified. We report a 43-year-old woman who presented with persistent nasal blockage, epistaxis, progressive right cheek swelling and ipsilateral proptosis. The aff