| MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options AW El-Hattab, AM Adesina, J Jones, F Scaglia Molecular genetics and metabolism 116 (1-2), 4-12, 2015 | 641 | 2015 |
| Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options AW El-Hattab, F Scaglia Neurotherapeutics 10 (2), 186-198, 2013 | 353 | 2013 |
| Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management PL Magoulas, AW El-Hattab Orphanet journal of rare diseases 7, 1-6, 2012 | 284 | 2012 |
| Mitochondrial DNA maintenance defects AW El-Hattab, WJ Craigen, F Scaglia Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1863 (6 …, 2017 | 270 | 2017 |
| Mitochondrial cardiomyopathies AW El-Hattab, F Scaglia Frontiers in Cardiovascular Medicine 3, 25, 2016 | 201 | 2016 |
| Therapies for mitochondrial diseases and current clinical trials AW El-Hattab, AM Zarante, M Almannai, F Scaglia Molecular genetics and metabolism 122 (3), 1-9, 2017 | 200 | 2017 |
| Restoration of impaired nitric oxide production in MELAS syndrome with citrulline and arginine supplementation AW El-Hattab, JW Hsu, LT Emrick, LJC Wong, WJ Craigen, F Jahoor, ... Molecular genetics and metabolism 105 (4), 607-614, 2012 | 169 | 2012 |
| Expanding the genetic heterogeneity of intellectual disability S Anazi, S Maddirevula, V Salpietro, YT Asi, S Alsahli, A Alhashem, ... Human genetics 136, 1419-1429, 2017 | 150 | 2017 |
| Disorders of carnitine biosynthesis and transport AW El-Hattab, F Scaglia Molecular genetics and metabolism 116 (3), 107-112, 2015 | 139 | 2015 |
| Inborn errors of metabolism AW El-Hattab Clinics in perinatology 42 (2), 413-439, 2015 | 134 | 2015 |
| Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases AW El-Hattab, J Suleiman, M Almannai, F Scaglia Molecular genetics and metabolism 125 (4), 315-321, 2018 | 127 | 2018 |
| Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects AW El-Hattab, FY Li, J Shen, BR Powell, EV Bawle, DJ Adams, E Wahl, ... Genetics in Medicine 12 (1), 19-24, 2010 | 119 | 2010 |
| Serine biosynthesis and transport defects AW El-Hattab Molecular genetics and metabolism 118 (3), 153-159, 2016 | 108 | 2016 |
| Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate WL Charng, E Karaca, Z Coban Akdemir, T Gambin, MM Atik, S Gu, ... BMC medical genomics 9, 1-14, 2016 | 105 | 2016 |
| Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin Y Bayram, E Karaca, ZC Akdemir, EO Yilmaz, GA Tayfun, H Aydin, ... The Journal of clinical investigation 126 (2), 762-778, 2016 | 104 | 2016 |
| MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations AW El-Hattab, FY Li, E Schmitt, S Zhang, WJ Craigen, LJC Wong Molecular genetics and metabolism 99 (3), 300-308, 2010 | 104 | 2010 |
| Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disorders AW El-Hattab, LT Emrick, WJ Craigen, F Scaglia Molecular genetics and metabolism 107 (3), 247-252, 2012 | 103 | 2012 |
| Carnitine inborn errors of metabolism M Almannai, M Alfadhel, AW El-Hattab Molecules 24 (18), 3251, 2019 | 93 | 2019 |
| Mitochondrial cytopathies AW El-Hattab, F Scaglia Cell Calcium 60 (3), 199-206, 2016 | 92 | 2016 |
| Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency FY Li, AW El‐Hattab, EV Bawle, RG Boles, ES Schmitt, F Scaglia, ... Human mutation 31 (8), E1632-E1651, 2010 | 91 | 2010 |
