A. O'meara

P. Connell, D. Brosnahan, A. Doyle, 2008, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation.

P. Veys, M. Renard, T. D. de Koning, 2017, Blood advances.

Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning.

A. Fischer, J. Tolar, J. Kurtzberg, 2013, Blood.

Risk factor analysis of outcomes after unrelated cord blood transplantation in patients with hurler syndrome.

J. Kurtzberg, M. Cavazzana‐Calvo, E. Gluckman, 2009, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Improved metabolic correction in patients with lysosomal storage disease treated with hematopoietic stem cell transplant compared with enzyme replacement therapy.

B. Bigger, J. E. Wraith, A. O’Meara, 2009, The Journal of pediatrics.

Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome

P. Veys, F. Wijburg, J. Boelens, 2006, Bone Marrow Transplantation.

Allogeneic bone marrow transplantation for lysosomal storage diseases

D. Frappaz, O. Ringdén, O. Brouwer, 1995, The Lancet.

Allogeneic bone marrow transplantation for lysosomal storage diseases. The European Group for Bone Marrow Transplantation.

D. Frappaz, O. Ringdén, O. Brouwer, 1995, Lancet.

Osteogenic sarcoma and Rothmund Thomson syndrome

P. Leavey, P. Smith, R. Sneath, 2005, Journal of Cancer Research and Clinical Oncology.

High-resolution analysis of chromosomal breakpoints and genomic instability identifies PTPRD as a candidate tumor suppressor gene in neuroblastoma.

John M Maris, Daniel Catchpoole, R. Stallings, 2006, Cancer research.

Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group.

W. Friedrich, A. Vellodi, A. Fasth, 1994, The Journal of pediatrics.

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

A. Fischer, E. Cirillo, A. Plebani, 2011, Blood.

Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q.

D Catchpoole, R. Stallings, A. Culhane, 2004, Carcinogenesis.

Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization.

R. Stallings, M. Mullarkey, M. McDermott, 2000, Cancer genetics and cytogenetics.

MicroRNA-204 increases sensitivity of neuroblastoma cells to cisplatin and is associated with a favourable clinical outcome

R. Stallings, A. Davidoff, K. Bryan, 2012, British Journal of Cancer.

Biallelic expression of the IGF2 gene in human breast disease.

N. Miller, A. McCann, I. Pedersen, 1996, Human molecular genetics.

Involvement of AMP-activated protein kinase in mediating pyrrolo-1,5-benzoxazepine–induced apoptosis in neuroblastoma cells

G. Campiani, S. Butini, D. Williams, 2016, Investigational New Drugs.

The novel pyrrolo-1,5-benzoxazepine, PBOX-6, synergistically enhances the apoptotic effects of carboplatin in drug sensitive and multidrug resistant neuroblastoma cells.

G. Campiani, S. Butini, D. Williams, 2014, Biochemical pharmacology.

N-myc oncogene amplification in paediatric tumours

A. O’Meara, S. Mcquaid, A. O'meara, 1990, Irish journal of medical science.

Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic disease

E. Wraith, K. Tylee, R. Wynn, 2007, Bone Marrow Transplantation.

Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma.

Michael Baudis, Holger Christiansen, Frank Speleman, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Widespread Dysregulation of MiRNAs by MYCN Amplification and Chromosomal Imbalances in Neuroblastoma: Association of miRNA Expression with Survival

D. Higgins, M. O'sullivan, R. Stallings, 2009, PloS one.

Primitive Myxoid Mesenchymal Tumor of Infancy: A Report of a Further Case with Locally Aggressive Behavior

M. McDermott, P. Eadie, D. Orr, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?

R. Stallings, M McDermott, A O'Meara, 2003, Cancer genetics and cytogenetics.

A new approach to the management of Broviac catheter infection.

F. Breatnach, A. O'meara, J. Rao, 1992, The Journal of hospital infection.

Identification and characterisation of an antithrombin III mutant (AT Dublin 2) with marginally decreased heparin reactivity.

M. Daly, A. O’Meara, R. Ball, 1989, Thrombosis research.

Identification and characterization of a new antithrombin III familial variant (AT Dublin) with possible increased frequency in children with cancer

M. Daly, A. O’Meara, F. Hallinan, 1987, British journal of haematology.

Langerhans cell histiocytosis — a 31 year review

P. Leavey, F. Breatnach, M. Varughese, 1991, Irish journal of medical science.

Minimal residual disease detection in childhood acute lymphoblastic leukaemia patients at multiple time‐points reveals high levels of concordance between molecular and immunophenotypic approaches

R. Stallings, M. Neat, A. O'marcaigh, 2009, British journal of haematology.

Increased antithrombin III concentration in children with acute lymphatic leukaemia receiving L-asparaginase therapy.

M. Daly, A. O’Meara, F. Hallinan, 1988, Medical and pediatric oncology.

Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation.

A. Fischer, A. Schulz, W. Friedrich, 2008, Blood.

New autoimmune diseases after cord blood transplantation: a retrospective study of EUROCORD and the Autoimmune Disease Working Party of the European Group for Blood and Marrow Transplantation.

M. Labopin, D. Farge, A. Vora, 2013, Blood.

Intensive enteral nutrition support in paediatric bone marrow transplantation

B. Bourke, A. O’Meara, A. Langdana, 2001, Bone Marrow Transplantation.

Paediatric umbilical cord blood transplantation.

A. O'marcaigh, E. Lawlor, A. O’Meara, 2012, Irish medical journal.

Extrarenal Wilms' tumor.

R. Fitzgerald, F. Breatnach, J. Kelleher, 1993, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

The management of thoracic inlet syndrome associated with Hurler's syndrome: a novel surgical technique.

L. Nölke, Rauf M Ahsan, S. Early, 2009, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Severe osteopenia with recurrent fractures after bone marrow transplant for Wiskott-Aldrich syndrome: a case report.

D. Reidy, E. Fogarty, I. Talkhani, 2000, Journal of pediatric orthopedics.

Ploidy changes between diagnosis and relapse in childhood renal tumours

A. Kelsey, E. Kay, S. Gururangan, 2004, Urological Research.

DNA quantitation of Wilms' tumour (nephroblastoma) using flow cytometry and image analysis.

M. Leader, S. Gururangan, A. O’Meara, 1992, Journal of clinical pathology.

Confirmation of FWT1 as a Wilms’ tumour susceptibility gene and phenotypic characteristics of Wilms’ tumour attributable to FWT1

Michael R. Stratton, Dick Variend, Richard Grundy, 1998, Human Genetics.

Evolution of unbalanced gain of distal chromosome 2p in neuroblastoma

R. Stallings, A. O’Meara, D. Catchpoole, 2004, Cytogenetic and Genome Research.

Identification of a leukocyte alloantigen with a high-frequency expression in leukemia patients.

T. Cotter, R. O'Connor, J. G. Bradley, 1989, Blood.

Incidence and prevalence of mucopolysaccharidosis type 1 in the Irish republic

S. Lynch, S. Lynch, D. Lambert, 2008, Archives of Disease in Childhood.

Mobility in Hurler Syndrome

E. Fogarty, F. Dowling, Colm C Taylor, 2006, Journal of pediatric orthopedics.

Ifosfamide nephrotoxicity in paediatric cancer patients

F. Breatnach, P. Deasy, J. Brady, 1994, European Journal of Pediatrics.

Hip dysplasia in Hurler's syndrome: orthopaedic management after bone marrow transplantation.

E. Fogarty, F. Dowling, D. Moore, 1996, Journal of pediatric orthopedics.

Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation.

K. White, R. Sakkers, P. Orchard, 2016, The Journal of bone and joint surgery. American volume.

A Long-term Retrospective Evaluation of Functional and Radiographic Outcomes of Pediatric Hip Surgery in Hurler Syndrome

K. Mulhall, E. Fogarty, E. Crushell, 2015, Journal of pediatric orthopedics.

Recognition of unusual presentation of natural killer cell leukemia

D. Reen, C. Gardiner, A. O’Meara, 1995, American journal of hematology.

Pharmacokinetically guided dosing of carboplatin in paediatric cancer patients with bilateral nephrectomy

A. Boddy, R. Grundy, A. Glaser, 2004, Cancer Chemotherapy and Pharmacology.

Recent experience with intensive combination chemotherapy for treatment of childhood acute lymphoblastic leukaemia

A. Staines, F. Breatnach, E. Vandenberghe, 1989, Irish journal of medical science.

The effect of methotrexate on in vitro immunoglobulin production.

D. Reen, A. O’Meara, J. Brazil, 1985, Journal of immunopharmacology.

Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation.

P. Veys, M. Renard, T. D. de Koning, 2017, Blood advances.

Indications for admission, treatment and improved outcome of paediatric haematology/oncology patients admitted to a tertiary paediatric ICU

A. O'marcaigh, K. Butler, D. Mannion, 2011, Irish journal of medical science.

Reactivity of P-glycoprotein monoclonal antibodies in childhood cancers.

T. Tsuruo, A. Imamura, P. Johnson, 1992, Oncology.

MicroRNA-184 inhibits neuroblastoma cell survival through targeting the serine/threonine kinase AKT2

M. O'sullivan, R. Stallings, P. Buckley, 2010, Molecular Cancer.

ACYCLOVIR FOR TREATMENT OF MUCOCUTANEOUS HERPES INFECTION IN A CHILD WITH LEUKÆMIA

W. Brigden, I. Hillary, A. O'meara, 1979, The Lancet.

Neuroblastoma--a surgical perspective.

P. Losty, R. Fitzgerald, F. Breatnach, 1993, European Journal of Surgical Oncology.

Terminal deoxynucleotidyl transferase positivity in neuroblastoma.

E. Lawlor, F. Breatnach, T. Finn, 1985, Acta Haematologica.

Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndrome.

M. O'sullivan, W. Reardon, R. Shahdadpuri, 2008, Clinical dysmorphology.

Excessive Blinking and Ataxia in a Child With Occult Neuroblastoma and Voltage-Gated Potassium Channel Antibodies

M. King, A. O’Meara, A. McKeon, 2012, Pediatrics.

Foot and Ankle Abnormalities in the Hurler Syndrome: Additions to the Phenotype

J. Noel, J. Kennedy, P. Kelly, 2013, Journal of pediatric orthopedics.

Reference Values for Urinary HMMA, HVA, Noradrenaline, Adrenaline, and Dopamine Excretion in Children Using Random Urine Samples and HPLC with Electrochemical Detection

W. Tormey, A. O’Meara, M. Fitzgibbon, 1992, Annals of clinical biochemistry.

Molecular cytogenetic analysis of recurrent unbalanced t(11;17) in neuroblastoma.

R. Stallings, A. O’Meara, F. Breatnach, 2004, Cancer genetics and cytogenetics.

Antithrombin Dublin (−3 Val → Glu): an N‐terminal variant which has an aberrant signal peptidase cleavage site

R. Carrell, M. Daly, P. Harper, 1990, FEBS letters.

The state of research into children with cancer across Europe: new policies for a new decade

R. Pieters, G. Lewison, G. Vassal, 2011, ecancermedicalscience.

Increased frequencies of the killer immunoglobulin-like receptor genes KIR2DL2 and KIR2DS2 are associated with neuroblastoma.

R. Stallings, S. Keating, C. Gardiner, 2015, Tissue antigens.

Successful allogeneic bone marrow transplant for Niemann–Pick disease type C2 is likely to be associated with a severe ‘graft versus substrate’ effect

A. Shabani, B. Bigger, J. E. Wraith, 2010, Journal of Inherited Metabolic Disease.

Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2.

J. E. Wraith, J. Imrie, E. O'Mahony, 2013, Molecular genetics and metabolism.

Fatal and unanticipated cardiorespiratory disease in a two-year-old child with hurler syndrome following successful stem cell transplant.

A. O’Meara, M. McDermott, R. Wynn, 2013, JIMD reports.

The Use of Complementary and Alternative Medicine by Irish Pediatric Cancer Patients

D. Graham, M. O'Reilly, M. Devins, 2013, Journal of pediatric hematology/oncology.

Persistent Complete Response After Single-agent Sunitinib Treatment in a Case of TFE Translocation Positive Relapsed Metastatic Pediatric Renal Cell Carcinoma

N. Sebire, Tanzina Chowdhury, A. Cherian, 2013, Journal of pediatric hematology/oncology.

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

S. Seal, M. Stratton, N. Rahman, 2005, Journal of Medical Genetics.

Evaluation of Ki-67 reactivity in neuroblastoma using paraffin embedded tissue.

P. Dervan, H. Magee, R. Ball, 1995, Pathology, Research and Practice.

Primary hepatic tumours in children: A 26—year review

S. Gururangan, E. Guiney, R. Fitzgerald, 1992, Journal of surgical oncology.

The Changing Role of Surgery in the Management of Rhabdomyosarcoma

A. Staines, R. Fitzgerald, F. Breatnach, 1992, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Genetic abnormalities in a pre and post-chemotherapy hepatoblastoma

R. Stallings, M. Mullarkey, M. McDermott, 2002, Cytogenetic and Genome Research.

Excessive Blinking and Ataxia in a Child With Occult Neuroblastoma and Voltage-Gated Potassium Channel Antibodies

M. King, A. McKeon, N. Allen, 2012, Pediatrics.

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

A. Fischer, E. Cirillo, A. Plebani, 2011, Blood.

Risk Factor Analysis of Outcomes after Unrelated Cord Blood Transplantation for Children with Hurler’s Syndrome. An Eurocord-Duke University Collaborative Study.

J. Kurtzberg, M. Cavazzana‐Calvo, E. Gluckman, 2007 .