Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maryam Amodu-Sanni"'
Autor:
Khadijat Omeneke Isezuo, Maryam Amodu-Sanni, Usman Muhammad Sani, Bilkisu Ilah Garba, Usman Muhammad Waziri, Murtala Muhammad Ahmad, Mikailu Abubakar Jangebe, Faruk Abubakar, Ibrahim Lawal Mada
Publikováno v:
Sahel Medical Journal, Vol 25, Iss 1, Pp 32-36 (2022)
Kwashi tremors or Kwashi shakes are uncommon neurological complications of unknown etiology seen in edematous forms of severe acute malnutrition (SAM) during rehabilitation phase of treatment. Four patients with SAM seen in our facility within a 30-m
Externí odkaz:
https://doaj.org/article/7101c24a8caf4a5bb3434e4ed3fa189e
Autor:
Fatima B. Jiya, Paul K. Ibitoye, Nma M. Jiya, Maryam Amodu-Sanni, Yahaya Mohammed, Dada M. Aquib, Lukman K. Coker
Publikováno v:
African Journal of Laboratory Medicine, Vol 10, Iss 1, Pp e1-e4 (2021)
Introduction: Emphysematous pyelonephritis is a life-threatening necrotising bacterial infection of the kidneys. It is rare among children and can be fatal if not promptly identified and treated. Case presentation: A 7-month-old male infant presente
Externí odkaz:
https://doaj.org/article/fdf6bff557f344b593ed69676c0adeef
Autor:
K. Omeneke Isezuo, Maryam Amodu-Sanni, Asma’u Adamu, B. Ilah Garba, F Jiya, Tahir Yusuf Bello, M. Omoshalewa Ugege, Baba Jibrin
Publikováno v:
Annals of Basic and Medical Sciences. 2
Background: Severe acute malnutrition (SAM) affects more than 20 million children worldwide, and it is highly prevalent in the African region where health systems are also coping with other highly prevalent infectious and non-infectious diseases. Wor
Autor:
Maryam Amodu-Sanni, Dada Muhammed Aquib, PK Ibitoye, FB Jiya, Lukman K. Coker, Nma M Jiya, Yahaya Mohammed
Publikováno v:
African Journal of Laboratory Medicine
African Journal of Laboratory Medicine, Vol 10, Iss 1, Pp e1-e4 (2021)
African Journal of Laboratory Medicine, Vol 10, Iss 1, Pp e1-e4 (2021)
Introduction: Emphysematous pyelonephritis is a life-threatening necrotising bacterial infection of the kidneys. It is rare among children and can be fatal if not promptly identified and treated. Case presentation: A 7-month-old male infant presented