Ahmad Alodaib

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud et al. · Brain · 2013 · 182 citations · Full text

Life Sciences, Genetics, Neurology +15

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1

Yiran Guo, Melissa Kartawinata, Jiankang Li et al. · Blood · 2014 · 119 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease

Ahmad Alodaib, Nara Sobreira, Wendy Gold et al. · European Journal of Human Genetics · 2016 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Physiological Perspectives on the Use of Triheptanoin as Anaplerotic Therapy for Long Chain Fatty Acid Oxidation Disorders

Evgenia Sklirou, Ahmad Alodaib, Steven F. Dobrowolski et al. · Frontiers in Genetics · 2021 · 38 citations · Full text

Life Sciences, Cardiology, Physiology +17

Lipidomics Profiling of Patients with Low Bone Mineral Density (LBMD)

Shereen M. Aleidi, Mysoon M. Al‐Ansari, Eman A. Alnehmi et al. · International Journal of Molecular Sciences · 2022 · 37 citations · Full text

Medicine, Endocrinology, Bone Metabolism +16