Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Abdullah A. Alhayani"'
Autor:
Ayed A. Shati, Own J. Al-Asmari, Abdullah A. Alhayani, Youssef A. Alqahtani, Salem A. Alshehri, Ibrahim A. Alhelali
Publikováno v:
Cardiology in the Young. 32:1677-1680
Diabetic ketoacidosis is one of the most serious and common complications of diabetes, with between 15 and 70% of new-onset type 1 diabetes mellitus worldwide presented with diabetic ketoacidosis. Supraventricular tachycardia, however, is an infreque
Autor:
Mohammad A. Alqahtani, Ayed A. Shati, Minjing Zou, Ali M. Alsuheel, Abdullah A. Alhayani, Saleh M. Al-Qahtani, Hessa M. Gilban, Brain F. Meyer, Yufei Shi
Publikováno v:
International Journal of Endocrinology, Vol 2015 (2015)
Congenital adrenal hyperplasia (CAH) due to steroid 11β-hydroxylase deficiency is the second most common form of CAH, resulting from a mutation in the CYP11B1 gene. Steroid 11β-hydroxylase deficiency results in excessive mineralcorticoids and andro
Externí odkaz:
https://doaj.org/article/f6789759e2874903a43b3c8cf939d15c
Autor:
Metrek Ali Almetrek, Abdullah A Alhayani, Ahmad A Alzoani, Mohammed A Algathradi, Saleh Fahad Abdullah Alqahtani
Publikováno v:
The Egyptian Journal of Hospital Medicine. 70:1117-1120
Background: Arterial tortuosity syndrome is one of the autosomal recessive diseases and caused by alterations (mutations) in the SLC2A10 gene. It is a rare disorder worldwide and in Saudi Arabia. Its prevalence is unknown. In the medical literature,
Autor:
Alqahtani, Saleh F.1 saleh.fahad777@gmail.com, Alzoani, Ahmad A.2, Algathradi, Mohammed A.1, Alhayani, Abdullah A.3, Almetrek, Metrek4
Publikováno v:
Egyptian Journal of Hospital Medicine. 2018, Vol. 70 Issue 7, p1117-1120. 4p.
Autor:
Shati, Ayed A., Al-Asmari, Own J., Alhayani, Abdullah A., Alqahtani, Youssef A., Alshehri, Salem A., Alhelali, Ibrahim A.
Publikováno v:
Cardiology in the Young; Oct2022, Vol. 32 Issue 10, p1677-1680, 4p