Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Walaa Alzahrani"'
Autor:
Murad Aljiffry, Walaa Alzahrani, Afnan Saeed, Israa Alsulami, Anas H. Alzahrani, Osman O. Al-Radi, Esraa A. Alshehrani, Fatemah Albugmi
Publikováno v:
Cureus
Introduction Perforated peptic ulcer disease (PPUD) is associated with a high postoperative mortality and morbidity rates especially within the first 90 days. The size and site of the ulcer may contribute to the prognosis of PPUD. In this study, we w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74db7b1b33de80cdf01e1d80923665d7
https://doi.org/10.7759/cureus.9790
https://doi.org/10.7759/cureus.9790
Autor:
Rasha Alharbi, Walaa Alzahrani, Dalia Sindi, Amani AlMutairi, Nisar Haider Zaidi, Dur Alsobhi, Yasmina Nezar Mohamed, Fatma K. Al-Thoubaity
Publikováno v:
Cureus
Objectives The heterogenicity of breast cancer (BC) is determined by the status of human epidermal growth factor receptor 2 (HER2/neu), estrogen receptor (ER), and progesterone receptor (PR). Triple-positive BC (TPBC) expresses the amplification/over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e90c52874a2adb2a5d79720a45c61d
http://europepmc.org/articles/PMC6935344
http://europepmc.org/articles/PMC6935344
Autor:
Sherif M. El-Desoky, Marwa Abdullah Bayazeed, Khalid Alhasan, Nada Abdullatif Hefni, Jameela A. Kari, Osama Y Safdar, Sara Nawfal Sharief, Walaa Alzahrani, Iman Ibrahim Nazer
Publikováno v:
World journal of pediatrics : WJP. 15(2)
Congenital and infantile nephrotic syndrome (CNS and INS) are rare inherited defects in glomerular filtration involving a variety of gene mutations. This study aimed to analyze all genetic mutations associated with congenital and infantile nephrotic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fce8737cc9e5301094122f1619621f24
https://pubmed.ncbi.nlm.nih.gov/30721404
https://pubmed.ncbi.nlm.nih.gov/30721404