Banu Kaya

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 21 publications

Endocrinopathies and growth in a UK cohort of children with transfusion dependent thalassaemia.

Endocrinopathies and growth in a UK cohort of children with transfusion dependent thalassaemia.

Journal: British journal of haematology

Published: April 08, 2026

Tocilizumab provides a potential therapeutic option for the management of hyperhaemolysis syndrome in sickle cell disease: A case series and brief narrative overview of the literature.

Tocilizumab provides a potential therapeutic option for the management of hyperhaemolysis syndrome in sickle cell disease: A case series and brief narrative overview of the literature.

Journal: Transfusion medicine (Oxford, England)

Published: May 09, 2025

UK Haemoglobin Disorders Peer Review: A Quality Standards-based review programme for sickle cell disease and thalassaemia.

UK Haemoglobin Disorders Peer Review: A Quality Standards-based review programme for sickle cell disease and thalassaemia.

Journal: British journal of haematology

Published: March 02, 2023

A non-injected opioid analgesia protocol for acute pain crisis in adolescents and adults with sickle cell disease.

A non-injected opioid analgesia protocol for acute pain crisis in adolescents and adults with sickle cell disease.

Journal: British journal of pain

Published: April 14, 2022

Association between Multi-Organ Involvement and Brain Injury in Cooled Newborns: A Statistical Approach.

Association between Multi-Organ Involvement and Brain Injury in Cooled Newborns: A Statistical Approach.

Journal: Developmental neuroscience

Published: September 14, 2021

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia.

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia.

Journal: Blood

Published: September 12, 2021

Guidelines for the monitoring and management of iron overload in patients with haemoglobinopathies and rare anaemias.

Guidelines for the monitoring and management of iron overload in patients with haemoglobinopathies and rare anaemias.

Journal: British journal of haematology

Published: May 26, 2021

Salvage of refractory post-transfusion hyperhaemolysis by targeting hyperinflammation and macrophage activation with tocilizumab.

Salvage of refractory post-transfusion hyperhaemolysis by targeting hyperinflammation and macrophage activation with tocilizumab.

Journal: Transfusion medicine (Oxford, England)

Published: December 31, 2020

Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients.

Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients.

Journal: Haematologica

Published: September 10, 2020

Evaluation of a Non-Parenteral Opioid Analgesia Protocol for Acute Sickle Cell Pain Episodes in Children.

Evaluation of a Non-Parenteral Opioid Analgesia Protocol for Acute Sickle Cell Pain Episodes in Children.

Journal: Journal of clinical medicine

Published: August 25, 2019

Development and validation of the Satisfaction with Treatment for Pain Questionnaire (STPQ) among patients with sickle cell disease.

Development and validation of the Satisfaction with Treatment for Pain Questionnaire (STPQ) among patients with sickle cell disease.

Journal: British journal of haematology

Published: December 11, 2018

Ticagrelor does not impact patient-reported pain in young adults with sickle cell disease: a multicentre, randomised phase IIb study.

Ticagrelor does not impact patient-reported pain in young adults with sickle cell disease: a multicentre, randomised phase IIb study.

Journal: British journal of haematology

Published: November 17, 2018

Showing 1-12 of 21

Last Updated: 09/26/2026