Cargando…

P130: PROVIDING ADEQUATE HEALTHCARE TO PEOPLE WITH HEMOGLOBINOPATHIES DURING THE PANDEMIC (COVID-19)

Detalles Bibliográficos
Autores principales:	Sophia Delicou, S, Aikaterini Xydaki, A, Konstantinos Manganas, K, Lucia Evliati, L, Chrysoula Kalkana, C, Michael Diamantidis, M, Achilles Manafas, A, Marianna Katsatou, M, Leonidas Roumpatis, L, Theodoros Aforozis, T
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Poster Presentations
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812063/ http://dx.doi.org/10.1097/01.HS9.0000821612.51153.9b

Ejemplares similares

Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review
por: Diamantidis, Michael D., et al.
Publicado: (2023)

5610178 SURVIVAL AND COMPLICATIONS IN PATIENTS WITH HEMOGLOBINOPATHIES: THE EXPERIENCE OF A SINGLE DEPARTMENT OF THALASSEMIA AND SICKLE DISEASE
por: Xydaki, X.A., et al.
Publicado: (2023)

Real‐world complication burden and disease management paradigms in transfusion‐related β‐thalassaemia in Greece: Results from ULYSSES, an epidemiological, multicentre, retrospective cross‐sectional study
por: Kattamis, Antonis, et al.
Publicado: (2023)

Twelve‐lead and signal‐averaged electrocardiographic parameters among beta‐thalassemia major patients
por: Patsourakos, Dimitrios, et al.
Publicado: (2020)

5613475 ADVERSE REACTIONS TO RBC TRANSFUSION: A SINGLE THALASSEMIA AND SICKLE CELL DISEASE DEPARTMENT’S EXPERIENCE
por: Xydaki, A.X., et al.
Publicado: (2023)

5610224 THE USE OF LUSPATERCEPT IN PATIENTS WITH β -THALASSAEMIA AND MULTIPLE SYSTEMIC COMPLICATIONS INCREASES HEMOGLOBIN LEVEL, DECREASES TRANSFUSION BURDEN, AND IS UNAFFECTED BY COMPLICATIONS. SINGLE THALASSEMIA AND SICKLE CELL DEPARTEMENT’S EXPERIENCE.
por: Manganas, K.M., et al.
Publicado: (2023)

P1517: REAL-WORLD COMPLICATION BURDEN AND DISEASE MANAGEMENT IN TRANSFUSION-DEPENDENT ADULTS WITH ΒETA-THALASSEMIA (Β-THAL) IN GREECE: FINAL RESULTS OF THE EPIDEMIOLOGICAL CROSS-SECTIONAL ULYSSES STUDY
por: Kattamis, A., et al.
Publicado: (2022)

P1508: LUSPATERCEPT REDUCES THE BURDEN OF RED BLOOD CELL TRANSFUSION IN PATIENTS WITH BETA -THALASSEMIA AND COMORBIDITIES: THE EXPERIENCE OF A SINGLE THALASSEMIA AND SICKLE CELL UNIT IN A UNIVERSITY HOSPITAL
por: Delicou, S., et al.
Publicado: (2022)

P1506: REAL-WORLD DATA ON THE USE OF LUSPATERCEPT IN GREEK PATIENTS WITH TRANSFUSION DEPENDENT THALASSEMIA
por: Delaporta, P., et al.
Publicado: (2022)

Updates in Hemoglobinopathies
por: Al-Tonbary, Youssef, et al.
Publicado: (2013)

Gene Therapy for Hemoglobinopathies
por: Cavazzana, Marina, et al.
Publicado: (2018)

Gene Therapy of the Hemoglobinopathies
por: Kunz, Joachim B., et al.
Publicado: (2020)

Hemoglobinopathy and COVID-19
por: Mungmunpuntipantip, Rujittika, et al.
Publicado: (2021)

Rare Combinational Hemoglobinopathies
por: Husan, Ammar, et al.
Publicado: (2022)

Gene Therapy in Thalassemia and Hemoglobinopathies
por: Breda, Laura, et al.
Publicado: (2009)

New approaches for cholestasis in hemoglobinopathies
por: Dhiman, Pratibha, et al.
Publicado: (2015)

Hemoglobinopathies in Iran: An Updated Review
por: Nasiri, Abolfazl, et al.
Publicado: (2020)

The hemoglobinopathies, molecular disease mechanisms and diagnostics
por: Harteveld, Cornelis L., et al.
Publicado: (2022)

PI-07: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES
por: P., KOUNTOURIS, et al.
Publicado: (2022)

P1481: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES
por: Kountouris, P., et al.
Publicado: (2022)

Sickle cell hemoglobinopathies in district Bhopal
por: Dangi, C. B. S., et al.
Publicado: (2010)

Prenatal Diagnosis of β-Thalassemias and Hemoglobinopathies.
por: Rosatelli, Maria Cristina, et al.
Publicado: (2009)

In utero hematopoietic cell transplantation for hemoglobinopathies
por: Derderian, S. Christopher, et al.
Publicado: (2015)

Guidelines for screening, diagnosis and management of hemoglobinopathies
por: Ghosh, Kanjaksha, et al.
Publicado: (2014)

Hemoglobinopathy and pediatrics in the time of COVID-19
por: Vilela, Thiago de Souza, et al.
Publicado: (2021)

Hemoglobinopathies: ocular manifestations in children and adolescents
por: Moussa, Omar, et al.
Publicado: (2021)

COULD COVID-19 BE A HEMOGLOBINOPATHY?
por: Shakoori, Tania Ahmed, et al.
Publicado: (2020)

Endocrinopathies complicating transfusion-dependent hemoglobinopathy
por: Al-Agha, Abdulmoein E., et al.
Publicado: (2020)

Endocrinopathies in Hemoglobinopathies: What Is the Role of Iron?
por: Evangelidis, Paschalis, et al.
Publicado: (2023)

5612571 EARLIER PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES BY CELOCENTESIS
por: Antonino Giambona, A.G., et al.
Publicado: (2023)

Pregnancy with a Severe Hemoglobinopathy: Unintended Consequences of Transfusions
por: Kim, David, et al.
Publicado: (2013)

Genetic Epidemiology and Preventive Healthcare in Multiethnic Societies: The Hemoglobinopathies
por: Giordano, Piero C., et al.
Publicado: (2014)

Pregnancy Complications in a-Thalassemia (Hemoglobinopathy H): A Case Study
por: Politou, Marianna, et al.
Publicado: (2018)

Transient Elastography (TE) is a Useful Tool for Assessing the Response of Liver Iron Chelation in Sickle Cell Disease Patients
por: Delicou, Sophia, et al.
Publicado: (2018)

Critical analysis of the neonatal screening program for hemoglobinopathies
por: Moreira, Raphaela Martins Muniz, et al.
Publicado: (2011)

Animal models of β-hemoglobinopathies: utility and limitations
por: McColl, Bradley, et al.
Publicado: (2016)

Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China
por: Huang, Hailong, et al.
Publicado: (2019)

Unexpected discovery of hemoglobinopathy C/β° thalassemia
por: Bouyarmane, Wafaa, et al.
Publicado: (2018)

Candidemia complicating biliary atresia in an infant with hemoglobinopathy
por: Kyriakidis, Ioannis, et al.
Publicado: (2019)

First trimester fetal aortic Doppler for hemoglobinopathies
por: Çetin, Cihan, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_ft5q74tsposdrq7e12qigjn0dc