| Treatment of E pstein B arr virus‐induced haemophagocytic lymphohistiocytosis with rituximab‐containing chemo‐immunotherapeutic regimens DB Chellapandian, R Das, K Zelley, SJ Wiener, H Zhao, DT Teachey, ... British journal of haematology 162 (3), 376-382, 2013 | 268 | 2013 |
| A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8 C Eidenschenk, J Dunne, E Jouanguy, C Fourlinnie, L Gineau, D Bacq, ... The American Journal of Human Genetics 78 (4), 721-727, 2006 | 144 | 2006 |
| Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference S Lobitz, P Telfer, E Cela, B Allaf, M Angastiniotis, C Backman Johansson, ... British journal of haematology 183 (4), 648-660, 2018 | 114 | 2018 |
| Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome C McMahon, A Will, P Hu, GN Shah, WS Sly, OP Smith Blood, The Journal of the American Society of Hematology 97 (7), 1947-1950, 2001 | 105 | 2001 |
| Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis MJ King, P Telfer, H MacKinnon, L Langabeer, C McMahon, P Darbyshire, ... Cytometry Part B: Clinical Cytometry: The Journal of the International …, 2008 | 97 | 2008 |
| Increased angiogenesis in bone marrow of children with acute lymphoblastic leukaemia has no prognostic significance MA Pule, C Gullmann, D Dennis, C McMahon, M Jeffers, OP Smith British Journal of Haematology 118 (4), 991-998, 2002 | 77 | 2002 |
| Central venous access devices in children with congenital coagulation disorders: complications and long‐term outcome C McMahon, J Smith, K Khair, R Liesner, IM Hann, OP Smith British journal of haematology 110 (2), 461-468, 2000 | 66 | 2000 |
| The impact of ultrasonographic placental architecture on antenatal course, labor and delivery in a low-risk primigravid population SM Cooley, JC Donnelly, T Walsh, C McMahon, J Gillan, MP Geary The Journal of Maternal-Fetal & Neonatal Medicine 24 (3), 493-497, 2011 | 40 | 2011 |
| The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency C McMahon, J Smith, C Goonan, M Byrne, OP Smith British journal of haematology 119 (3), 789-791, 2002 | 39 | 2002 |
| South‐east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects H Guizouarn, F Borgese, N Gabillat, P Harrison, JS Goede, C McMahon, ... British journal of haematology 152 (5), 655-664, 2011 | 34 | 2011 |
| Protein C and free protein S in children with sickle cell anemia A Piccin, C Murphy, E Eakins, A Kinsella, C McMahon, OP Smith, ... Annals of hematology 91 (10), 1669-1671, 2012 | 32 | 2012 |
| Newborn screening for sickle cell disease in Europe Y Daniel, J Elion, B Allaf, C Badens, MJ Bouva, I Brincat, E Cela, ... International Journal of Neonatal Screening 5 (1), 15, 2019 | 31 | 2019 |
| Composition and significance of splenic Gamna-Gandy bodies in sickle cell anemia A Piccin, H Rizkalla, O Smith, C McMahon, C Furlan, C Murphy, G Negri, ... Human pathology 43 (7), 1028-1036, 2012 | 31 | 2012 |
| Liver biopsy in Irish hepatitis C‐infected patients with inherited bleeding disorders C McMahon, R Pilkington, EO Shea, D Kelleher, OP Smith British Journal of Haematology 109 (2), 354-359, 2000 | 31 | 2000 |
| The treatment of flexion contracture of the knee using the Ilizarov technique in a child with haemophilia B PD Kiely, C McMahon, OP Smith, DP Moore Haemophilia 9 (3), 336-339, 2003 | 28 | 2003 |
| Sickle cell disease and dental treatment A Piccin, P Fleming, E Eakins, E McGovern, OP Smith, C McMahon J Ir Dent Assoc 54 (2), 75-79, 2008 | 27 | 2008 |
| Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH‐binding lobe of cytochrome b5 reductase MJ Percy, LJ Crowley, CA Davis, MF McMullin, G Savage, J Hughes, ... British journal of haematology 129 (6), 847-853, 2005 | 27 | 2005 |
| Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification M Cotter, T Connell, E Colhoun, OP Smith, C McMahon Journal of Pediatric Hematology/Oncology 27 (2), 115-117, 2005 | 26 | 2005 |
| CALR mutations are rare in childhood essential thrombocythemia. SE Langabeer, K Haslam, C McMahon Pediatric Blood & Cancer 61 (8), 1523-1523, 2014 | 21 | 2014 |
| Intranasal fentanyl versus intravenous morphine in the emergency department treatment of severe painful sickle cell crises in children: study protocol for a randomised … MJ Barrett, J Cronin, A Murphy, S McCoy, J Hayden, T Grant, A Wakai, ... Trials 13 (1), 1-7, 2012 | 20 | 2012 |
