Epidemiology of childhood type 1 diabetes mellitus in Nile Delta, northern Egypt-a retrospective study MAEM El-Ziny, NAB Salem, AK El-Hawary, NM Chalaby, AAE Elsharkawy Journal of clinical research in pediatric endocrinology 6 (1), 9, 2014 | 109 | 2014 |
Association of ghrelin and leptin with reproductive hormones in constitutional delay of growth and puberty MM El-Eshmawy, IA Abdel Aal, AK El Hawary Reproductive Biology and Endocrinology 8, 1-6, 2010 | 73 | 2010 |
Helicobacter pylori infection might be responsible for the interconnection between type 1 diabetes and autoimmune thyroiditis MM El-Eshmawy, AK El-Hawary, SS Abdel Gawad, AA El-Baiomy Diabetology & metabolic syndrome 3, 1-7, 2011 | 56 | 2011 |
Leptin, insulin and thyroid hormones in a cohort of Egyptian obese Down syndrome children: a comparative study S Yahia, RM El-Farahaty, AK El-Hawary, MA El-Hussiny, H Abdel-Maseih, ... BMC endocrine disorders 12, 1-7, 2012 | 49 | 2012 |
Effect of tactile/kinesthetic massage therapy on growth and body composition of preterm infants MA Elmoneim, HA Mohamed, A Awad, A El-Hawary, N Salem, R El Helaly, ... European journal of pediatrics 180, 207-215, 2021 | 31 | 2021 |
Safety and metabolic impact of Ramadan fasting in children and adolescents with type 1 diabetes A El-Hawary, N Salem, A Elsharkawy, A Metwali, A Wafa, N Chalaby, ... Journal of Pediatric Endocrinology and Metabolism 29 (5), 533-541, 2016 | 27 | 2016 |
HLA-DQB1* alleles and genetic susceptibility to type 1 diabetes mellitus YM Mosaad, FA Auf, SS Metwally, AA Elsharkawy, AK El-Hawary, ... World journal of diabetes 3 (8), 149, 2012 | 25 | 2012 |
Bone mineral status in children with epilepsy: biochemical and radiologic markers B Hasaneen, RM Elsayed, N Salem, A Elsharkawy, N Tharwat, K Fathy, ... Journal of Pediatric Neurosciences 12 (2), 138-143, 2017 | 24 | 2017 |
Bone mineral density in newly diagnosed children with neuroblastoma YA Al‐Tonbary, MA El‐Ziny, AA Elsharkawy, AK El‐Hawary, R El‐Ashry, ... Pediatric blood & cancer 56 (2), 202-205, 2011 | 23 | 2011 |
Fanconi Bickel Syndrome: Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families M Al-Haggar, O Sakamoto, A Shaltout, A El-Hawary, Y Wahba, ... Case Reports in Nephrology 2011 (1), 754369, 2011 | 16 | 2011 |
Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome M Al‐Haggar, N Salem, Y Wahba, N Ahmad, L Jonard, D Abdel‐Hady, ... Pediatric Diabetes 16 (4), 305-316, 2015 | 15 | 2015 |
Quality of life of children with bronchial asthma and their caregivers: a hospital-based study AH El-Gilany, T El Desoky, AK El-Hawary, M Farrag Prog Med Sci 2 (1), 1-8, 2018 | 13 | 2018 |
Serum interferon-alpha level in first degree relatives of systemic lupus erythematosus patients: Correlation with autoantibodies titers D Shahin, AM El-Refaey, AK El-Hawary, AA Salam, S Machaly, ... Egyptian Journal of Medical Human Genetics 12 (2), 139-146, 2011 | 12 | 2011 |
Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience W Laimon, M El-Ziny, A El-Hawary, A Elsharkawy, NAB Salem, ... Acta Diabetologica 58 (12), 1689-1700, 2021 | 10 | 2021 |
Prepubertal gynecomastia is not always idiopathic: case series and review of the literature W Laimon, A El-Hawary, H Aboelenin, M Elzohiri, S Abdelmaksoud, ... European Journal of Pediatrics 180, 977-982, 2021 | 9 | 2021 |
The emergence of systemic lupus erythematosus in hypothyroid patients: two case reports and mini review A Bakr, W Laimon, MA El-Ziny, A Hammad, AK El-Hawary, AA Elsharkawy, ... Lupus 23 (8), 825-828, 2014 | 9 | 2014 |
Acute flaccid paralysis in a patient with sacral dimple M Mostafa, N Nasef, T Barakat, AK El-Hawary, H Abdel-Hady World Journal of Clinical Pediatrics 2 (3), 26, 2013 | 6 | 2013 |
Bisphenol-a and risk of obesity among a sample of Egyptian children: role of adiponectin as biomarker of exposure HM Abo El-Atta, AM El-Mansoury, AK El-Hawary, MEM Abdel-Naby, ... Mansoura Journal of Forensic Medicine and Clinical Toxicology 26 (1), 39-52, 2018 | 5 | 2018 |
Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations M Al-Haggar, A Taranta, A El-Hawary, A Al-Said, AA Shaban, Y Wahba Middle East Journal of Medical Genetics 1 (2), 71-75, 2012 | 4 | 2012 |
Assessment of bone mineral density in children with congenital cyanotic heart disease AA Elsharkawy, AK El-Hawary, GA Alsawah, HM Aboelenin, MH Awad Cardiology in the Young 32 (1), 71-76, 2022 | 3 | 2022 |