| A large kindred with X‐linked neutropenia with an I294T mutation of the Wiskott‐Aldrich syndrome gene K Beel, MM Cotter, J Blatny, J Bond, G Lucas, F Green, V Vanduppen, ... British journal of haematology 144 (1), 120-126, 2009 | 121 | 2009 |
| Coagulation indices in very preterm infants from cord blood and postnatal samples E Neary, N McCallion, B Kevane, M Cotter, K Egan, I Regan, C Kirkham, ... Journal of Thrombosis and Haemostasis 13 (11), 2021-2030, 2015 | 66 | 2015 |
| Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARS JP Casey, S Slattery, M Cotter, AA Monavari, I Knerr, J Hughes, EP Treacy, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2015 | 61 | 2015 |
| High responding factor VIII inhibitors in mild haemophilia–is there a link with recent changes in clinical practice? Cotter, Byrne Haemophilia 6 (2), 113-115, 2000 | 52 | 2000 |
| Laboratory Coagulation Parameters in Extremely Premature Infants Born Earlier than 27 Gestational Weeks upon Admission to a Neonatal Intensive Care Unit E Neary, I Okafor, F Al-Awaysheh, C Kirkham, K Sheehan, C Mooney, ... Neonatology 104 (3), 222-227, 2013 | 32 | 2013 |
| 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 |
| Successful treatment with rituximab and mycophenolate mofetil of refractory autoimmune hemolytic anemia post‐hematopoietic stem cell transplant for dyskeratosis congenita due … N O'Connell, M Goodyer, M Gleeson, L Storey, M Williams, M Cotter, ... Pediatric transplantation, 2013 | 24 | 2013 |
| Successful use of gemtuzumab ozogamicin in a child with relapsed CD33-positive acute lymphoblastic leukaemia. M Cotter, S Rooney, A O'Marcaigh, OP Smith British journal of haematology 122 (4), 2003 | 22 | 2003 |
| Catalogue of inherited disorders found among the Irish Traveller population SA Lynch, E Crushell, DM Lambert, N Byrne, K Gorman, MD King, ... Journal of Medical Genetics 55 (4), 233-239, 2018 | 20 | 2018 |
| Sickle cell disease: time for a targeted neonatal screening programme. C Gibbons, R Geoghegan, H Conroy, S Lippacott, D O'Brien, P Lynam, ... Irish Medical Journal, 2015 | 19 | 2015 |
| Successful treatment of a refractory verruca in a child with acute lymphoblastic leukaemia with topical cidofovir AM Tobin, M Cotter, AD Irvine, B Kirby The British journal of dermatology 152 (2), 386-388, 2005 | 18 | 2005 |
| Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF2 mutation. M Gleeson, A O'Marcaigh, M Cotter, D Brosnahan, T Vulliamy, OP Smith British journal of haematology 159 (5), 2012 | 15 | 2012 |
| Breaking bad news--parents' experience of learning that their child has leukaemia. J Oshea, O Smith, A O'Marcaigh, C McMahon, R Geoghegan, M Cotter Irish medical journal 100 (9), 588-590, 2007 | 13 | 2007 |
| Perinatal factors affecting coagulation parameters at birth in preterm and term neonates: a retrospective cohort study H Go, H Ohto, KE Nollet, N Kashiwabara, K Ogasawara, M Chishiki, ... American Journal of Perinatology 36 (14), 1464-1470, 2019 | 11 | 2019 |
| Successful treatment of acute Epstein–Barr virus infection associated with X‐linked lymphoproliferative disorder with rituximab J Bond, R Shahdadpuri, C Mc Mahon, A O'marcaigh, M Cotter, O Smith Pediatric Blood & Cancer 49 (5), 761-762, 2007 | 11 | 2007 |
| Tinzaparin is safe and effective in the management of hemodialysis catheter thrombosis C Quinlan, M Bates, M Cotter, M Riordan, M Waldron, A Awan ASAIO journal 58 (3), 288-290, 2012 | 9 | 2012 |
| Plasmacytoma occurring in scar tissue. M Cotter, H Enright British journal of haematology 121 (5), 2003 | 9 | 2003 |
| A retrospective study of myeloid leukaemia in children with Down syndrome in Ireland GP Dowling, A Piccin, KT Gavin, DR Betts, A Malone, M Cotter, A Sills, ... Irish Journal of Medical Science (1971-) 189, 979-984, 2020 | 6 | 2020 |
| The challenges of pregnancy management in pyridoxine nonresponsive homocystinuria: The Irish experience C Hart, J McNulty, M Cotter, F Al Jasmi, E Crushell, AA Monavari JIMD reports 61 (1), 34-41, 2021 | 5 | 2021 |
| Sideroblastic anaemia and primary adrenal insufficiency due to a mitochondrial respiratory chain disorder in the absence of mtDNA deletion MJ O'Grady, AA Monavari, M Cotter, NP Murphy Case Reports 2015, bcr2014208514, 2015 | 5 | 2015 |
Naomi McCallionAssociate Professor, RCSI在 rcsi.com 的电子邮件经过验证
