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of 25
pro vyhledávání: '"Ahmadu, Baba Usman"'
Autor:
Ahmadu Baba Usman, Pembi Emmanuel, Dogo Belmont Manchan, Akoma chinyere, Ovansa Emmanuel Onimisi, Mava Yakubu, Kenji Hirayama
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 195 (2019)
Pellagra is a nutritional disorder of niacin deficiency which is characterized by triad of dermatitis, diarrhea and dementia. It is often seen in a state of poor nutrition among alcoholics, homeless and patients suffering from malabsorption. Though s
Externí odkaz:
https://doaj.org/article/ac7ad071820f49f5bcd147e9f447ad13
Autor:
Muhammad Faruk Bashir, Hassan Abdullahi Elechi, Mohammed Garba Ashir, Adamu Ibrahim Rabasa, David Nadeba Bukbuk, Ahmadu Baba Usman, Modu Gofama Mustapha, Mohammad Arab Alhaji
Publikováno v:
Journal of Tropical Medicine, Vol 2016 (2016)
Background. Tetanus toxoid immunisation of pregnant mother has remained the most effective strategy in eliminating neonatal tetanus. Impaired production and/or transplacental transfer of antibodies may affect the effectiveness of this strategy. We st
Externí odkaz:
https://doaj.org/article/b24e2a198f764cbcb23052904e1dc009
Autor:
Ahmadu Baba Usman, Abdulrasheed A Nasir, Simon Pius, Awwal Abubakar, Talba Aliyu, Mustapha Bello
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Despite advances in obstetric and neonatal care, subgaleal haemorrhage continues to create significant challenges to health personnel, especially in poor human resource/ facility settings, where a specialist may not always be readily available, there
Autor:
Simon Pius, Adzu Yusuf, Yakubu Sani, Harifarta Difirwiti, Ahmadu Baba Usman, Tope Bello, Mustapha Bello
Publikováno v:
Open Journal of Pediatrics. :58-65
Background: Achondrogenesis type II is a lethal form of osteochondrodysplasia characterized by short trunk, disproportionately large head, prominent forehead, micrognathia, extreme micromelia, anasarca, large abdomen and poor ossification of the bone
Autor:
Pembi Emmanuel, Apollos Nachanuya, Ovansa Emmanuel Onimisi, AM Abubakar, HA Nggada, Ahmadu Baba Usman, Adewale O. Oyinloye
Publikováno v:
Journal of Nepal Paediatric Society. 38:122-124
DOI: https://doi.org/10.3126/jnps.v38i2.19623 Duchene muscular dystrophy is an x-linked recessive genetic disorder which present with progressive muscle weakness in children. It is often complicated by child becoming wheelchair bound by age 12. This
Akademický článek
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Autor:
Dogo Belmont Manchan, Pembi Emmanuel, Ovansa Emmanuel Onimisi, Akoma chinyere, Kenji Hirayama, Ahmadu Baba Usman, Mava Yakubu
Publikováno v:
The Pan African Medical Journal
Pellagra is a nutritional disorder of niacin deficiency which is characterized by triad of dermatitis, diarrhea and dementia. It is often seen in a state of poor nutrition among alcoholics, homeless and patients suffering from malabsorption. Though s
Autor:
Ahmadu, Baba Usman1 ahmadu4u2003@yahoo.com, Nnanubumom, Andy Angela1, Mohammed, Hussaini1, Sharah, Joshua Habila1, Evelyn, Bitrus Elesa1, Francis, Zoba Joseph1
Publikováno v:
Internet Journal of Medical Update. Jan2014, Vol. 9 Issue 1, p41-44. 4p. 2 Charts.
Publikováno v:
Ethiopian Journal of Health Sciences. Jul2013, Vol. 23 Issue 2, p174-177. 4p.
Publikováno v:
Journal of Pediatric Infectious Diseases. May2013, Vol. 8 Issue 2, p93-96. 4p.