H. Alshaalan

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

Olfat Al-Harazi, N. Kaya, D. Çolak, 2014, Journal of Medical Genetics.

Extraneural Metastasis of an Ependymoma: A Rare Occurrence

A. Kashgari, A. Alassiri, A. Alzahrani, 2014, The neuroradiology journal.

Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases.

Robert W. Taylor, N. Kaya, B. Plecko, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Mucolipidosis II: first report from Saudi Arabia

M. Alfadhel, W. Eyaid, M. A. Al Balwi, 2013, Annals of Saudi medicine.

Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism.

D. Trujillano, A. Rolfs, M. Alfadhel, 2015, JIMD reports.

Thoracic, abdominal and pelvic CT and US imaging features in children with hemophagocytic lymphohistocytosis

D. Manson, R. Schneider, P. Cox, 2015 .

Unusual Testicular Ultrasound Findings in a Child with Henoch-Schönlein Purpura

H. Alshaalan, Ahmad S. Alzahrani, Hanan Mohammad Shaher, 2013 .

Early Prediction of COVID-19 Ventilation Requirement and Mortality from Routinely Collected Baseline Chest Radiographs, Laboratory, and Clinical Data with Machine Learning

M. Rashid, Yahya Bokhari, Abdulrhman Aljouie, 2021, Journal of multidisciplinary healthcare.

Hepatobiliary anomalies in conjoined twins.

M. Zamakhshary, A. Al-Rabeeah, A. Al-Qahtani, 2011, Journal of pediatric surgery.

Haematological and radiological-based prognostic markers of COVID-19

S. Mir, F. Alhumaydhi, Abdulrhman Aljouie, 2021, Journal of Infection and Public Health.