Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hafsat W Idris"'
Publikováno v:
Nigerian Journal of Paediatrics. 48:50-53
Gangliosidoses belong to the group of genetic lipid metabolism disorders, caused by defects of lysosome enzymes, inherited as an autosomal recessive trait. Gangliosidosis GM1 is caused by the deficiency of the acid beta-galactosidase (GLB11) resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93e65217ca45914d7864b17e75e52aaf
https://doi.org/10.4314/njp.v48i1.10
https://doi.org/10.4314/njp.v48i1.10
Publikováno v:
Sub-Saharan African Journal of Medicine. 5:29
Xerophthalmia is an important cause of preventable blindness in Nigerian children. Vitamin A deficiency is not the only cause of staphyloma. The vitamin A deficiency can lead to degenerative changes with subsequent softening of the cornea and protrus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70d4cbd02159aee93305a241ae5987b8
https://doi.org/10.4103/ssajm.ssajm_23_17
https://doi.org/10.4103/ssajm.ssajm_23_17
Autor:
Olumide Olatokunbo Jarrett, M Ugochi Ibekwe, AO Oduwole, Bolanle Fetuga, Tamunopriye Jaja, Omotayo Adesiyun, Hafsat W Idris, Kayode Adeniran, Salma Suwaid, Jerome B. E. Elusiyan, Iroro Yarhere, NA Akani, Yahaya S. Alkali, Oliver Blankenstein
Publikováno v:
Hormone research in paediatrics. 85(1)
Background: Congenital hypothyroidism is a common congenital endocrine disorder prevailing all over the world. No nationwide screening exists for any sub-Saharan country. We present normative cord and capillary thyroid-stimulating hormone (TSH) value
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6e4a217de06452de97e4c21f900b60b
https://pubmed.ncbi.nlm.nih.gov/26670140
https://pubmed.ncbi.nlm.nih.gov/26670140
Publikováno v:
Sub-Saharan African Journal of Medicine. 4:87
Currently, up to 65 million Africans have chronic hepatitis B (CHB) infection, with the majority acquiring it in the first 5 years of life and living in Nigeria. Lamivudine is generally accepted for use as the first-line treatment of CHB in children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67330927f66ff70b5aa50e1d59f7466a
https://doi.org/10.4103/ssajm.ssajm_21_17
https://doi.org/10.4103/ssajm.ssajm_21_17