Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bawazir, Maryam A."'
Autor:
Kentab, Amal, Muddathir, H.H., Salih, M.A., Mushiba, Aziza M., Zada, A.P., Bamajboor, Mohammed S., Zameer, Sadique, AlBassam, Fahad, Mahmoud, Adel, Alnawfal, A.A., AlAmr, Mushari, Bawazir, Maryam, Al Rumayyan, Ahmed, Al-Twaijri, Waleed, Alrifai, Muhammed Talal, Al Hajjaj, Sumayah, Saleh, Mohammed M., Hamhom, Abdulrahim M., Al-Otaibi, Ali, AlGhamdi, Malak, Housawi, Yousef, Aljadhai, Yaser I., Alameer, Seham, Almannai, Mohammed, Jad, Lamyaa A., Alwadei, Ali H., Tabassum, Sadia, Alsaman, Abdulaziz, AlAsmari, Ali, Al Mutairi, Fuad, Althiyab, Hamad, Bashiri, Fahad A., AlHumaidi, Suzan, Alfadhel, Majid, Mink, Jonathan W., AlHashim, Aqeela, Faqeih, Eissa A.
Publikováno v:
In Pediatric Neurology June 2024 155:149-155
Akademický článek
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Autor:
Alsubaie, Sarah S., Gosadi, Ibrahim M., Alsaadi, Basma M., Albacker, Nouf B., Bawazir, Maryam A., Bin-Daud, Nada, Almanie, Waad B., Alsaadi, Muslim M., Alzamil, Fahad A.
Publikováno v:
Saudi Medical Journal
Objectives: To assess the prevalence of vaccine hesitancy and its determinants among Saudi parents. In addition, we explored the relationship between vaccine hesitancy and child’s immunization status. Methods: A cross-sectional study was conducted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b16673290fdd5b4dec954ea146332dd
http://europepmc.org/articles/PMC6969619
http://europepmc.org/articles/PMC6969619
Permanent neonatal diabetes may occur either in isolation or associated with multi-organ syndromes. It is caused by mutations in the genes responsible for pancreatic β cell mass or function. We report new cases of consanguineous parents from Saudi A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=sharePrprorg::9abc1c743ae43759103daeb1d3a54a12
Autor:
Mir, Ali, Almudhry, Montaha, Alghamdi, Fouad, Albaradie, Raidah, Ibrahim, Mona, Aldurayhim, Fatimah, Alhedaithy, Abdullah, Alamr, Mushari, Bawazir, Maryam, Mohammad, Sahar, Abdelhay, Salma, Bashir, Shahid, Housawi, Yousef
Publikováno v:
Human Genetics; Jan2022, Vol. 141 Issue 1, p81-99, 19p