A stable intermediate in the equilibrium unfolding of Escherichia coli citrate synthase.

Por Ayed, A., Duckworth, H. W.
Publicado em 1999

Solution structure of a conserved C-terminal domain of p73 with structural homology to the SAM domain.

Por Chi, S W, Ayed, A, Arrowsmith, C H
Publicado em 1999

Myelodysplastic Syndrome with Myelofibrosis Transformed to a Precursor B-Cell Acute Lymphoblastic Leukemia: A Case Report with Review of the Literature

Por Algarni, Ayed A., Akhtari, Mojtaba, Fu, Kai
Publicado em 2012

Gastrointestinal autonomic nerve tumor of the stomach

Por Meshikhes, Abdul-Wahed N., Al-Garni, Ayed A., Al-Momen, Sami A., Al-Nahawi, Mamdouh, Abu Subaih, Jawad
Publicado em 2014

Study of a noncovalent trp repressor: DNA operator complex by electrospray ionization time-of-flight mass spectrometry.

Por Potier, N., Donald, L. J., Chernushevich, I., Ayed, A., Ens, W., Arrowsmith, C. H., Standing, K. G., Duckworth, H. W.
Publicado em 1998

Effectiveness of laparoscopic fundoplication for gastro-oesophageal reflux.

Por Khoursheed, M. A., Al-Asfoor, M., Al-Shamali, M., Ayed, A. K., Gupta, R., Dashti, H. M., Behbehani, A. I.
Publicado em 2001

Frequency and Management of Acute Poisoning Among Children Attending an Emergency Department in Saudi Arabia

Por Mansour Tobaiqy, Bandar A. Asiri, Ahmed H. Sholan, Yahya A. Alzahrani, Ayed A. Alkatheeri, Ahmed M. Mahha, Shamsia S. Alzahrani, Katie MacLure
Publicado em 2020-10-01

Circulating microRNAs as potential diagnostic biomarkers for osteoporosis

Por Mandourah, Abdullah Y., Ranganath, Lakshminarayan, Barraclough, Roger, Vinjamuri, Sobhan, Hof, Robert Van’T, Hamill, Sandra, Czanner, Gabriela, Dera, Ayed A., Wang, Duolao, Barraclough, Dong L.
Publicado no Sci Rep (2018)

Occurrence of Diarrhea and Feeding Practices among Children below Two Years of Age in Southwestern Saudi Arabia

Por Ayed A. Shati, Shamsun N. Khalil, Khalid A. Asiri, Abdulaziz Ahmed Alshehri, Yazeed A. Deajim, Mohammad S. Al-Amer, Hassan J. Alshehri, Abdulaziz Abdullah Alshehri, Fahad S. Alqahtani
Publicado em 2020-01-01

A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy

Por 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
Publicado em 2015-01-01

A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy

Por Alqahtani, Mohammad A., Shati, Ayed A., Zou, Minjing, Alsuheel, Ali M., Alhayani, Abdullah A., Al-Qahtani, Saleh M., Gilban, Hessa M., Meyer, Brain F., Shi, Yufei
Publicado no Int J Endocrinol (2015)