| RETRACTED ARTICLE: Endothelin-1 and leptin as markers of intrauterine growth restriction MAS Nezar, AMA El-Baky, OAS Soliman, HAS Abdel-Hady, AM Hammad, ... The Indian Journal of Pediatrics 76 (5), 485-488, 2009 | 75 | 2009 |
| Vitamin E and N‐Acetylcysteine as Antioxidant Adjuvant Therapy in Children with Acute Lymphoblastic Leukemia Y Al-Tonbary, M Al-Haggar, R El-Ashry, S El-Dakroory, H Azzam, A Fouda Advances in Hematology 2009 (1), 689639, 2009 | 58 | 2009 |
| Sirenomelia (symelia apus) with Potter's syndrome in connection with gestational diabetes mellitus: a case report and literature review M Al-Haggar, S Yahia, D Abdel-Hadi, F Grill, A Al Kaissi African health sciences 10 (4), 2010 | 46 | 2010 |
| Biofeedback and cognitive behavioral therapy for Egyptian adolescents suffering from chronic fatigue syndrome MS Al-Haggar, ZA Al-Naggar, MA Abdel-Salam Journal of pediatric neurology 4 (03), 161-169, 2006 | 43 | 2006 |
| A novel homozygous p. Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome M Al-Haggar, A Madej-Pilarczyk, L Kozlowski, JM Bujnicki, S Yahia, ... European journal of human genetics 20 (11), 1134-1140, 2012 | 42 | 2012 |
| Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats HIH El-Sayyad, MMS Al-Haggar, HA El-Ghawet, IHM Bakr Nutrition 30 (3), 326-336, 2014 | 36 | 2014 |
| Impact of long-term oral iron supplementation in breast-fed infants N Abdelrazik, M Al-Haggar, H Al-Marsafawy, H Abdel-Hadi, R Al-Baz, ... The Indian Journal of Pediatrics 74 (8), 739-745, 2007 | 28 | 2007 |
| Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia A Settin, M Al Haggar, T Al Dosoky, R Al Baz, NM Abdelrazik, M Fouda, ... The Indian Journal of Pediatrics 74 (3), 255-263, 2007 | 28 | 2007 |
| Cystinosis as a lysosomal storage disease with multiple mutant alleles: phenotypic-genotypic correlations M Al-Haggar World journal of nephrology 2 (4), 94, 2013 | 24 | 2013 |
| MRI CSF flowmetry in evaluation of different neurological diseases N Ahmad, D Salama, M Al-Haggar Egyptian Journal of Radiology and Nuclear Medicine 52 (1), 53, 2021 | 23 | 2021 |
| Screening for G6PD Mediterranean mutation among Egyptian neonates with high or prolonged jaundice A Settin, M Al-Haggar, R Al-Baz, H Yousof, N Osman Haema 9 (1), 83-90, 2006 | 23 | 2006 |
| Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family M Al-Haggar, A Bakr, T Tajima, K Fujieda, A Hammad, O Soliman, ... Clinical and experimental nephrology 13 (4), 288-294, 2009 | 22 | 2009 |
| Disruptive behavior in Down syndrome children: a cross-sectional comparative study S Yahia, M El-Hadidy, AH El-Gilany, D Amdel-Hady, Y Wahba, ... Annals of Saudi medicine 34 (6), 517-521, 2014 | 20 | 2014 |
| Bioinformatics in high throughput sequencing: application in evolving genetic diseases MM Al-Haggar, BA Khair-Allaha, MM Islam, ASA Mohamed J Data Mining Genomics Proteomics 4 (131), 2153-0602.1000131, 2013 | 20 | 2013 |
| 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 | 19 | 2015 |
| Single nucleotide polymorphism of IL4C-590T and IL4RA 175V and immunological parameters in Egyptian asthmatics with different clinical phenotypes M Zedan, A Bakr, B Shouman, H Zaghloul, M Al-Haggar, M Zedan, ... J Allergy Ther 5 (189), 2, 2014 | 15 | 2014 |
| p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome M Al-Haggar, S Yahia, K Damjanovich, N Ahmad, I Hamada, ... The Indian Journal of Pediatrics 78 (1), 103-105, 2011 | 15 | 2011 |
| Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia: Cases from Mansoura, Egypt A Settin, M Al Haggar, T Al Dosok, R Al Baz, N Abdelrazik, M Fouda, ... Hematology 11 (5-6), 341-349, 2006 | 15 | 2006 |
| 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 | 14 | 2011 |
| Detection of beta-thalassaemia mutations using primer-specific amplification compared to reversed dot blot hybridization technique in Egyptian cases AA Settin, MM Al-Haggar, M Neamatallah, AM Al-Said, MM Hafez Haema 9 (3), 401-409, 2006 | 14 | 2006 |
