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The Journal of Hand Surgery, European Volume|September 30, 2009
Narakas classification of obstetric brachial plexus palsy revisitedM M Al-Qattan, A A F El-Sayed, A Y Al-Zahrani, et al.The Journal of Hand Surgery, European Volume|February 26, 2010
Obstetric brachial plexus palsy in newborn babies of diabetic and non-diabetic mothersM M Al-Qattan, A A F El-Sayed, A Y Al-Zahrani, et al.The Journal of Hand Surgery, European Volume|December 25, 2009
Obstetric brachial plexus palsy: a comparison of affected infants delivered vaginally by breech or cephalic presentationM M Al-Qattan, A A F El-Sayed, A Y Al-Zahrani, et al.BMC Medical Education|October 26, 2012
Constructing a question bank based on script concordance approach as a novel assessment methodology in surgical educationSalah A Aldekhayel, Nahar A Alselaim, Mohi Eldin Magzoub, et al.Biomed Research International|November 30, 2013
Salamander-derived, human-optimized nAG protein suppresses collagen synthesis and increases collagen degradation in primary human fibroblastsMohammad M Al-Qattan, Medhat K Shier, Mervat M Abd-Alwahed, et al.Biology Letters|February 6, 2020
Prehistoric baseline reveals substantial decline of oyster reef condition in a Gulf of Mexico conservation priority areaStephen G Hesterberg, Gregory S Herbert, Thomas J Pluckhahn, et al.American Journal of Human Genetics|May 20, 2014
Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDHRanad Shaheen, Zuhair Rahbeeni, Amal Alhashem, et al.Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|January 21, 2021
Screening for PIK3CA mutations among Saudi women with ovarian cancerWedad Saeed Al-Qahtani, Manal Abduallah Alduwish, Ebtesam M Al-Olayan, et al.Journal of Biomedical Materials Research. Part B, Applied Biomaterials|October 7, 2021
Toward allogenizing a xenograft: Xenogeneic cardiac scaffolds recellularized with human-induced pluripotent stem cells do not activate human naïve neutrophilsReem S Al-Hejailan, Razan H Bakheet, Mashael M Al-Saud, et al.American Journal of Human Genetics|March 26, 2019
Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in HumansRanad Shaheen, Nan Jiang, Fatema Alzahrani, et al.Pageof 42