Hesham Alshaalan

<i>ISCA2</i> mutation causes infantile neurodegenerative mitochondrial disorder

Zuhair N. Al‐Hassnan, Mazhor Aldosary, Majid Alfadhel et al. · Journal of Medical Genetics · 2014 · 98 citations

Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism

Majid Alfadhel, Muhammad Talal Alrifai, Daniel Trujillano et al. · JIMD Reports · 2015 · 55 citations · Full text

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

Abdulrhman Aljouie, Ahmed Almazroa, Yahya Bokhari et al. · Journal of Multidisciplinary Healthcare · 2021 · 44 citations · Full text

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

Majid Alfadhel, Marwan Nashabat, Muhammad Talal Alrifai et al. · European Journal of Paediatric Neurology · 2017 · 27 citations

Isca2 Defect, Ten New Cases, Pathology +1

Pilot-randomized study on intraventricular hemorrhage with midline versus lateral head positions.

Sameer Y Al-Abdi, Maha S Nojoom, Hesham Alshaalan et al. · PubMed · 2011 · 18 citations

Interventional Neuroradiology, Pilot-randomized Study, Medicine +11