Multidisciplinary care in haemoglobinopathies

Multidisciplinary care in haemoglobinopathies

While most complications are related to haemoglobinopathies and their treatment, it is also possible to observe substantial differences in comorbidities’ onset and seriousness which depend also to the different HPs genotypes. These differences should be carefully considered when health authorities s...

Full description

Bibliographic Details
Main Authors:	Adriana Ceci, Laura Mangiarini, Fedele Bonifazi, Rossella Conte, on behalf of the HTA-THAL Multiregional Registry
Format:	Article
Language:	English
Published:	MDPI AG 2014-12-01
Series:	Thalassemia Reports
Subjects:	haemoglobinopathies HPs genotypes Thalassaemia major Sickle cell disease Transfusion dependent Non-transfusion dependent.
Online Access:	http://www.pagepressjournals.org/index.php/thal/article/view/4875

Similar Items

Iron in haemoglobinopathies and rare anaemias
by: John Porter
Published: (2014-12-01)

A comprehensive review of hydroxyurea for β-haemoglobinopathies: the role revisited during COVID-19 pandemic
by: Nirmani Yasara, et al.
Published: (2021-03-01)

TIF Standards for Haemoglobinopathy Reference Centres
by: Michael Angastiniotis, et al.
Published: (2022-12-01)

Bridging the gaps in newborn screening programmes: Challenges and opportunities to detect haemoglobinopathies in Africa
by: Seth Twum, et al.
Published: (2023-12-01)

Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review
by: Eihab A. Subahi, et al.
Published: (2022-12-01)

The Outcomes of Patients with Haemoglobin Disorders in Cyprus: A Joined Report of the Thalassaemia International Federation and the Nicosia and Paphos Thalassaemia Centres (State Health Services Organisation)
by: Michael Angastiniotis, et al.
Published: (2022-11-01)

Red Cell Alloantibodies in Multi - Transfused Patients of Beta Thalassaemia Major
by: Madeeha Rehan
Published: (2015-06-01)

Haemoglobinopathies in Referred Cases for Haemoglobin Electrophoresis in a Tertiary Care Teaching Hospital
by: Maha Tariq, et al.
Published: (2019-12-01)

Antenatal screening for haemoglobinopathies in primary care: a cohort study and cluster randomised trial to inform a simulation model. The Screening for Haemoglobinopathies in First Trimester (SHIFT) trial
by: E Dormandy, et al.
Published: (2010-04-01)

Estimation of Microalbuminuria in Children with Beta Thalassaemia Major: A Cross-sectional Study
by: YB Arun, et al.
Published: (2024-03-01)

Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB , HFE, SLC40A1, and TFR2 genes
by: Ruwangi Dissanayake, et al.
Published: (2022-06-01)

Genetic investigation of haemoglobinopathies in a large cohort of asymptomatic individuals reveals a higher carrier rate for β-thalassaemia in Sichuan Province (Southwestern China)
by: Xia Yu, et al.
Published: (2021-03-01)

Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies
by: Stella Tamana, et al.
Published: (2022-12-01)

Haemoglobinopathies encountered at Khoula Hospital, Oman A retrospective study
by: Gihan Adly, et al.
Published: (2008-03-01)

Alloimmunization in Transfusion Dependent Thalassaemic Patients.
by: Saad H. Ahmed, et al.
Published: (2010-04-01)

Transfusion Transmitted Hepatitis B Virus among Multitransfused Thalassaemic Children in a Tertiary Health Care Centre in Bangladesh
by: Ishaque Mahmud Kamal, et al.
Published: (2012-07-01)

Non-Transfusion-Dependent Thalassaemia: A Panoramic Survey from Pathophysiology to Treatment
by: Abdul-Hamid A. Bazarbachi, et al.
Published: (2016-12-01)

Body iron status of children and adolescents with transfusion dependent β-thalassaemia: trends of serum ferritin and associations of optimal body iron control
by: Tharindi Suriapperuma, et al.
Published: (2018-08-01)

A study on transfusion-transmitted infections and other complications amongst children with beta-thalassaemia major attending a tertiary care institution in Kolkata
by: Archi Chandra, et al.
Published: (2023-01-01)

Routine management, healthcare resource use and patient and carer‐reported outcomes of patients with transfusion‐dependent β‐thalassaemia in the United Kingdom: A mixed methods observational study
by: Farrukh Shah, et al.
Published: (2021-11-01)

Transfusion in Haemoglobinopathies: Review and recommendations for local blood banks and transfusion services in Oman
by: Arwa Z. Al-Riyami, et al.
Published: (2018-04-01)

Evaluation of Serum Transaminases Levels In Transfused β-Thalssaemia Major Patients
by: Saad A. Mustafa
Published: (2010-04-01)

Pregnancy in women with thalassemia: challenges and solutions
by: Petrakos G, et al.
Published: (2016-09-01)

Haemoglobin E/Beta Thalassaemia- A Study in BSMMU
by: Md Abdul Aziz, et al.
Published: (2010-04-01)

Haematopoietic stem cell transplantation in thalassaemia major: A narrative review
by: Rabeya Yousuf, et al.
Published: (2023-01-01)

Management of liver complications in haemoglobinopathies
by: Pierre Brissot, et al.
Published: (2014-12-01)

Economic burden in the management of transfusion-dependent thalassaemia patients in Malaysia from a societal perspective
by: Asrul Akmal Shafie, et al.
Published: (2021-04-01)

Haemoglobinopathy prevention program in Turkey
by: D. Canatan
Published: (2011-12-01)

Demographic and Clinicoradiological Presentation of Tuberculosis in Patients with Sickle Cell Haemoglobinopathy: A Cross-sectional Study
by: Ranjan Kumar Patel, et al.
Published: (2022-07-01)

Link between Genotype and Multi-Organ Iron and Complications in Children with Transfusion-Dependent Thalassemia
by: Antonella Meloni, et al.
Published: (2022-03-01)

Addressing adherence to treatment: a longstanding concern. The patients’ perspective
by: Mahmoud Hadipour Dehshal
Published: (2014-12-01)

The forgotten people with thalassemia in the time of COVID-19: South Asian perspective
by: Mohammad Sorowar Hossain, et al.
Published: (2020-09-01)

Proportion of Hypogonadism in Transfusion-Dependent Thalassemia Patients and Its Contributing Factors
by: Dian Anindita Lubis, et al.
Published: (2024-01-01)

Knowledge and practices on childhood anaemia, thalassaemia and iron deficiency among mothers of children aged between 6 and 59 months in a suburban area of Sri Lanka
by: Ruwan Samararathna, et al.
Published: (2022-12-01)

CRISPR-CAS 9 AND ITS APPLICATION AS THERAPEUTICS FOR β-HAEMOGLOBINOPATHIES
by: Manoj Kumar Tripathi, et al.
Published: (2023-06-01)

Impact of COVID-19 Pandemic on Pre-Transfusion Hemoglobin Level and Frequency of Transfusion in Transfusion-Dependent Thalassemia Patients in Indonesia
by: Ludi Dhyani Rahmartani, et al.
Published: (2022-12-01)

Oxidative Stress (Malondialdehyde) in Adults Beta-Thalassemia Major and Intermedia: Comparison Between Before and After Blood Transfusion and Its Correlation with Iron Overload
by: Atmakusuma TD, et al.
Published: (2021-10-01)

Burden of Congenital Haemolytic Anaemias among the Rural Paediatric Population of Central India
by: Manal Ashraf Ali, et al.
Published: (2022-08-01)

Incidence of Thalassaemia in Jammu and Kashmir, India
by: Roopali Jandial, et al.
Published: (2021-01-01)

Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania
by: Heavenlight Christopher, et al.
Published: (2021-12-01)