List of works - Corrina McMahon

A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8.

scientific article

A prenatal origin of childhood essential thrombocythaemia ⬇️

scientific article published on August 16, 2013

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphoma

scientific article published on 06 July 2013

CALR mutations are rare in childhood essential thrombocythemia

scientific article published on 13 February 2014

Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification.

scientific article

Composition and significance of splenic Gamna-Gandy bodies in sickle cell anemia ⬇️

scientific article published on November 12, 2011

Congenital JAK2V617F polycythemia vera: where does the genotype-phenotype diversity end?

scientific article published on 01 November 2008

Distinct driver mutation profiles of childhood and adolescent essential thrombocythemia.

scientific article published on 17 August 2014

Esophageal strictures during treatment for acute lymphoblastic leukemia

scientific article published on 01 March 2010

Increased angiogenesis in bone marrow of children with acute lymphoblastic leukaemia has no prognostic significance

scientific article published on 01 September 2002

Intranasal fentanyl versus intravenous morphine in the emergency department treatment of severe painful sickle cell crises in children: study protocol for a randomised controlled trial.

scientific article

Protein C and free protein S in children with sickle cell anemia

scientific article published on 21 March 2012

Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser

scientific article published on 17 April 2014

Sickle cell disease and dental treatment.

scientific article published on April 2008

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

scientific article published on 23 January 2011

Successful use of protease inhibitors in HIV‐infected haemophilia patients ⬇️

scientific article published on June 1, 1998

The JAK2 V617F mutation in pediatric myeloproliferative neoplasms: how and when?

scientific article published on 02 January 2014

The correlation of ultrasonographic placental architecture with placental histology in the low-risk primigravid population

scientific article published in September 2013

The impact of positive acquired thrombophilia serology on ultrasound, obstetric outcome and the placenta in a low-risk primigravid population

scientific article published on March 2011

The molecular landscape of childhood myeloproliferative neoplasms.

scientific article published on 12 June 2014

The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency

scientific article published on 01 December 2002

The treatment of flexion contracture of the knee using the Ilizarov technique in a child with haemophilia B ⬇️

scientific article published on May 1, 2003

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

scientific article published in July 2008

Vaccine-Preventable Admissions to an Irish Paediatric Intensive Care

scientific article published on 10 May 2017

List of works by Corrina McMahon

A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8.

A prenatal origin of childhood essential thrombocythaemia ⬇️

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphoma

CALR mutations are rare in childhood essential thrombocythemia

Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification.

Composition and significance of splenic Gamna-Gandy bodies in sickle cell anemia ⬇️

Congenital JAK2V617F polycythemia vera: where does the genotype-phenotype diversity end?

Distinct driver mutation profiles of childhood and adolescent essential thrombocythemia.

Esophageal strictures during treatment for acute lymphoblastic leukemia

Increased angiogenesis in bone marrow of children with acute lymphoblastic leukaemia has no prognostic significance

Intranasal fentanyl versus intravenous morphine in the emergency department treatment of severe painful sickle cell crises in children: study protocol for a randomised controlled trial.

Protein C and free protein S in children with sickle cell anemia

Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser

Sickle cell disease and dental treatment.

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

Successful use of protease inhibitors in HIV‐infected haemophilia patients ⬇️

The JAK2 V617F mutation in pediatric myeloproliferative neoplasms: how and when?

The correlation of ultrasonographic placental architecture with placental histology in the low-risk primigravid population

The impact of positive acquired thrombophilia serology on ultrasound, obstetric outcome and the placenta in a low-risk primigravid population

The molecular landscape of childhood myeloproliferative neoplasms.

The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency

The treatment of flexion contracture of the knee using the Ilizarov technique in a child with haemophilia B ⬇️

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

Vaccine-Preventable Admissions to an Irish Paediatric Intensive Care