Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Abdullah A. Alhayani"'
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:
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:
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:
Al-Hassnan ZN; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia; Department of Medical Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia. Electronic address: zhassnan@kfshrc.edu.sa., Al-Fayyadh M; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Al-Ghamdi B; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Shafquat A; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Mallawi Y; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Al-Hadeq F; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Tulbah S; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Shinwari ZMA; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Almesned A; Prince Sultan Cardiac Center, Qassim, Saudi Arabia., Alakhfash A; Prince Sultan Cardiac Center, Qassim, Saudi Arabia., Al Fadly F; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Hersi AS; Cardiac Sciences Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia., Alhayani A; Maternity and Children Hospital, Abha, Saudi Arabia., Al-Hashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia., Arafah D; Maternity and Children Hospital, Makkah, Saudi Arabia., Dzimiri N; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Meyer B; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Rababh M; Cardiovascular Genetics Program, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Al-Manea W; Heart Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Publikováno v:
Heart rhythm [Heart Rhythm] 2017 Aug; Vol. 14 (8), pp. 1191-1199. Date of Electronic Publication: 2017 Apr 22.