| Thalassemia intermedia: An overview RM Shawky, TM Kamal Egyptian Journal of Medical Human Genetics 13 (3), 245-255, 2012 | 62 | 2012 |
| Bone mineral density and calcium metabolism in adolescents with beta-thalassemia major. AA Tantawy, M El Kholy, T Moustafa, HH Elsedfy Pediatric endocrinology reviews: PER 6, 132-135, 2008 | 40 | 2008 |
| Study of the C677T and 1298AC polymorphic genotypes of MTHFR Gene in autism spectrum disorder F El-Baz, M Abd El-Aal, TM Kamal, AA Sadek, AA Othman Electronic Physician 9 (9), 5287, 2017 | 31 | 2017 |
| Cytokine gene polymorphism [tumor necrosis factor-alpha (–308), IL-10 (–1082), IL-6 (–174), IL-17F, 1RaVNTR] in pediatric patients with primary immune thrombocytopenia and … GM Mokhtar, NMS El-Beblawy, AA Adly, NS Elbarbary, TM Kamal, ... Blood Coagulation & Fibrinolysis 27 (3), 313-323, 2016 | 26 | 2016 |
| Study of genotype–phenotype correlation of methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in a sample of Egyptian autistic children RM Shawky, F El-baz, TM Kamal, RM Elhossiny, MA Ahmed, GH El Nady Egyptian Journal of Medical Human Genetics 15 (4), 335-341, 2014 | 22 | 2014 |
| Angiotensinogen M235T gene polymorphism is a genetic determinant of cerebrovascular and cardiopulmonary morbidity in adolescents with sickle cell disease MS ElAlfy, FSE Ebeid, TM Kamal, DS Eissa, EAR Ismail, SH Mohamed Journal of Stroke and Cerebrovascular Diseases 28 (2), 441-449, 2019 | 13 | 2019 |
| Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene ZA El-Kabbany, RT Hamza, DM Shinkar, TM Kamal, RI Abdelmageed, ... International Journal of Pediatrics and Adolescent Medicine 6 (1), 21-24, 2019 | 11 | 2019 |
| Klf10 gene, a secondary modifier and a pharmacogenomic biomarker of hydroxyurea treatment among patients with hemoglobinopathies MS Elalfy, NHK El Sherif, TM Kamal, NH Aly Journal of Pediatric Hematology/Oncology 39 (3), e155-e162, 2017 | 11 | 2017 |
| Dopamine D4 receptor gene polymorphism in a sample of Egyptian children with attention-deficit hyperactivity disorder (ADHD) F ElBaz Mohamed, TM Kamal, SS Zahra, MAH Khfagy, AM Youssef Journal of child neurology 32 (2), 188-193, 2017 | 9 | 2017 |
| Genotyping of mannose-binding lectin (MBL2) codon 54 and promoter alleles in Egyptian infants with acute respiratory tract infections RM Shawky, SM Abd El-Fattah, TM Kamal, MA Esa, GH El Nady Egyptian Journal of Medical Human Genetics 15 (1), 31-38, 2014 | 8 | 2014 |
| Molecular characterization of X chromosome fragility in idiopathic mental retardation HAH Omar, TM Kamal, HS Abd-Alkhalek, GH El Nady, MSZ Salem Egyptian Journal of Medical Human Genetics 17 (2), 165-172, 2016 | 6 | 2016 |
| enzymatic Preparation of low-Phenylalanine Formula Derived from Skim Milk Hydrolysate for Phenyl ketonuric Patients AE Shehata, MNI El-Magdoub, TM Kamal, HA Mohamed Egyptian Journal of Medical Human Genetics 9 (1), 51-71, 2008 | 6 | 2008 |
| A study of dopamine D2 receptor Taq1 a alleles in children with attention-deficit hyperactivity disorder MM Moro, HH El-Gebaly, EA Zaky, TM Kamal Current Pediatric Research 23 (1), 9-16, 2019 | 5 | 2019 |
| A study of human killer cell immunoglobulin-like receptor and multidrug resistance gene polymorphisms in children with immune thrombocytopenia NMS El-Beblawy, NS Elbarbary, TM Kamal, PM Mahmoud Clinical and Applied Thrombosis/Hemostasis 22 (5), 429-440, 2016 | 5 | 2016 |
| Prenatal diagnosis of β-thalassemia via automated DHPLC analysis of fetal cells in maternal circulation RM Shawky, AS Khalifa, GM Mokhtar, MM Rifaat, TM Kamal, NA Elhawary, ... Egypt J Med Hum Genet 4 (2), 1-8, 2003 | 5 | 2003 |
| Biochemical and molecular study of cystic fibrosis among high risk group patients with chronic lung disease RM Shawky, KA Abd El Khalek, SM Abdel Fattah, SE Moselhi, MM Rifaat, ... Egypt J Med Genet 4 (1), 97-112, 2003 | 4 | 2003 |
| Genotypic spectrum of 21-hydroxylase deficiency in an endogamous population RAA Mahmoud, NH Amr, NN Toaima, TM Kamal, HH Elsedfy Journal of Endocrinological Investigation, 1-13, 2022 | 3 | 2022 |
| Assessment of glucokinase regulatory protein rs1260326 gene variant polymorphism in the development of nonalcoholic fatty liver disease among Egyptian obese children M Eladawy, TM Kamal, K Ibrahim, F Elbaz Egyptian Liver Journal 6 (2), 37-41, 2016 | 3 | 2016 |
| Protein substitution to produce a processed cheese with high branched-chain amino acids of medical and genetic importance HAM El-Shazly, RA Awad, EAY Essawy, TM Kamal, WM Salama Egyptian Journal of Medical Human Genetics 11 (2), 121-133, 2010 | 3 | 2010 |
| A lymphotoxin-alpha gene polymorphism and asthma in Egyptian children NA El Hawary, TM Kamal The Egyptian Journal of Medical Human Genetics 7 (1), 7-14, 2006 | 3 | 2006 |
