| β-thalassemia distribution in the old world: an ancient disease seen from a historical standpoint V De Sanctis, C Kattamis, D Canatan, AT Soliman, H Elsedfy, M Karimi, ... Mediterranean journal of hematology and infectious diseases 9 (1), 2017 | 383 | 2017 |
| Efficacy and safety of a novel combination of two oral chelators deferasirox/deferiprone over deferoxamine/deferiprone in severely iron overloaded young beta thalassemia major … MS Elalfy, AM Adly, Y Wali, S Tony, A Samir, YI Elhenawy European Journal of Haematology 95 (5), 411-420, 2015 | 121 | 2015 |
| Characterization of PRF1, STX11 and UNC13D genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis AC Horne, KG Ramme, E Rudd, C Zheng, Y Wali, Z Al‐Lamki, A Gürgey, ... British journal of haematology 143 (1), 75-83, 2008 | 115 | 2008 |
| Impact of the coronavirus disease 2019 (COVID‐19) pandemic on pediatric oncology care in the Middle East, North Africa, and West Asia region: a report from the Pediatric … R Saab, A Obeid, F Gachi, H Boudiaf, L Sargsyan, K Al‐Saad, ... Cancer 126 (18), 4235-4245, 2020 | 87 | 2020 |
| Physical fitness indices and anthropometrics profiles in schoolchildren with sickle cell trait/disease H Moheeb, YA Wali, MS El‐Sayed American journal of hematology 82 (2), 91-97, 2007 | 73 | 2007 |
| Preliminary data on COVID-19 in patients with hemoglobinopathies: a multicentre ICET-A study V De Sanctis, D Canatan, JLV Corrons, M Karimi, S Daar, C Kattamis, ... Mediterranean journal of hematology and infectious diseases 12 (1), 2020 | 62 | 2020 |
| Orbital infarction in sickle cell disease A Ganesh, S Al-Zuhaibi, A Pathare, R William, R Al-Senawi, A Al-Mujaini, ... American journal of ophthalmology 146 (4), 595-601. e1, 2008 | 61 | 2008 |
| Decreased bone mineral density in prepubertal children with sickle cell disease: correlation with growth parameters, degree of siderosis and secretion of growth factors AT Soliman, H Bererhi, A Darwish, MM Alzalabani, Y Wali, B Ansari Journal of tropical pediatrics 44 (4), 194-198, 1998 | 60 | 1998 |
| Pulsed high-dose dexamethasone therapy in children with chronic idiopathic thrombocytopenic purpura YA Wali, ZA Lamki, W Shah, M Zacharia, A Hassan Pediatric hematology and oncology 19 (5), 329-335, 2002 | 56 | 2002 |
| Coagulation abnormalities in type 1 Gaucher disease in children A Deghady, I Marzouk, A El-Shayeb, Y Wali Pediatric hematology and oncology 23 (5), 411-417, 2006 | 53 | 2006 |
| A prospective study of soft-tissue ultrasonography in sickle cell disease patients with suspected osteomyelitis RR William, SS Hussein, WD Jeans, YA Wali, ZA Lamki Clinical Radiology 55 (4), 307-310, 2000 | 53 | 2000 |
| Vincristine‐induced neuropathy in pediatric patients with acute lymphoblastic leukemia in Oman: Frequent autonomic and more severe cranial nerve involvement HF Nazir, A AlFutaisi, M Zacharia, M Elshinawy, ST Mevada, A Alrawas, ... Pediatric blood & cancer 64 (12), e26677, 2017 | 50 | 2017 |
| Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and α-thalassemia trait YA Wali, Z Al-Lamki, SS Hussein, H Bererhi, D Kumar, S Wasifuddin, ... Pediatric hematology and oncology 19 (7), 491-500, 2002 | 47 | 2002 |
| Evaluation of early corticosteroid therapy in management of pediatric septic shock in pediatric intensive care patients: a randomized clinical study A El-Nawawy, D Khater, H Omar, Y Wali The Pediatric infectious disease journal 36 (2), 155-159, 2017 | 45 | 2017 |
| Craving for ice and iron-deficiency anemia: a case series from Oman YM Osman, YA Wali, OM Osman Pediatric hematology and oncology 22 (2), 127-131, 2005 | 42 | 2005 |
| A comparison of two transfusion regimens in the perioperative management of children with sickle cell disease undergoing adenotonsillectomy YA Wali, HA Okbi, RA Abri Pediatric hematology and oncology 20 (1), 7-13, 2003 | 40 | 2003 |
| Impact of Burden of thalassemia major on health-related quality of Life in omani children ST Mevada, M Al Saadoon, M Zachariah, AH Al Rawas, Y Wali Journal of pediatric hematology/oncology 38 (5), 384-388, 2016 | 36 | 2016 |
| Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area MH Qari, Y Wali, MH Albagshi, M Alshahrani, A Alzahrani, IA Alhijji, ... Orphanet journal of rare diseases 8, 1-12, 2013 | 34 | 2013 |
| Effect of poloxamer 188 vs placebo on painful vaso-occlusive episodes in children and adults with sickle cell disease: a randomized clinical trial JF Casella, BA Barton, J Kanter, LV Black, S Majumdar, A Inati, Y Wali, ... Jama 325 (15), 1513-1523, 2021 | 33 | 2021 |
| Sevuparin for the treatment of acute pain crisis in patients with sickle cell disease: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial BJ Biemond, A Tombak, Y Kilinc, M Al-Khabori, M Abboud, M Nafea, ... The Lancet Haematology 8 (5), e334-e343, 2021 | 32 | 2021 |
