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Journal Articles

Thalassemia in europe: A cross-border real-world data analysis from the radeep registry

Blood (2025) 146 (Supplement 1): 4696.

https://doi.org/10.1182/blood-2025-4696

Published: 2025

Journal Articles

Bridging the gap: Global caregiver perspectives on awareness, motivators, and barriers to clinical trial participation in sickle cell disease

John James, Johnny Mahlangu, Raffaella Colombatti, Cassandra Trimnell, Darren Fleetwood, Emma Tan, Biree Andemariam

Blood (2025) 146 (Supplement 1): 2952.

https://doi.org/10.1182/blood-2025-2952

Published: 2025

Journal Articles

Qualitative interviews exploring the patient experience of fatigue in individuals with sickle cell disease (SCD), thalassemia, and pyruvate kinase (PK) deficiency

Blood (2025) 146 (Supplement 1): 7971.

https://doi.org/10.1182/blood-2025-7971

Published: 2025

Journal Articles

Data validation and quality framework for building a european multimodal real-world dataset for clinical outcome research in sickle cell disease

Blood (2025) 146 (Supplement 1): 4443.

https://doi.org/10.1182/blood-2025-4443

Published: 2025

Journal Articles

Sickle cell disease in europe: A cross-border real-world data analysis from the radeep registry

Blood (2025) 146 (Supplement 1): 179.

https://doi.org/10.1182/blood-2025-179

Published: 2025

Journal Articles

Patient-driven insights in sickle cell disease: Results from a global survey informing public health strategies

Mariangela Pellegrini, Baba Inusa, Raffaella Colombatti, Issom David-Zacharie, Mariane de Montalembert, Piel Fréderic B., Béatrice Gulbis, Smith Lan-Lan, Maria Del Mar Mañú Pereira

Blood (2025) 146 (Supplement 1): 4441.

https://doi.org/10.1182/blood-2025-4441

Published: 2025

Journal Articles

Implementing patient-centered PROMs in sickle cell disease care: A european consensus approach

Anna Collado Gimbert, Betzabel Cajiao Garcia, Raffaella Colombatti, Mariane de Montalembert, Elisabetta Mezzalira, Eduard Van Beers, Maria Del Mar Mañú Pereira

Blood (2025) 146 (Supplement 1): 2666.

https://doi.org/10.1182/blood-2025-2666

Published: 2025

Journal Articles

Sickle cell disease trials redefined: Toward unified clinical endpoints through international consensus

Mohamed Yassin, Nirmish Shah, Andrew Campbell, Salam Al-Kindi, Wally Smith, Charles Jonassaint, Miguel Abboud, Raffaella Colombatti, Dipty Jain, Halima Bello-Manga, Mariane de Montalembert, Ana Silva-Pinto, Steven Okoli, Abdelaziz Fahem, Biree Andemariam

Blood (2025) 146 (Supplement 1): 1166.

https://doi.org/10.1182/blood-2025-1166

Published: 2025

Journal Articles

How People with Sickle Cell Disease Rate Motivators is Associated with the Likelihood of Wanting to Participate in a Clinical Trial: Findings from the Global LISTEN Survey

Biree Andemariam, Johnny Mahlangu, Raffaella Colombatti, John Waller, Samar Al-Behaisi, Gareth Morrell, John James

Blood (2024) 144 (Supplement 1): 1137.

https://doi.org/10.1182/blood-2024-200009

Published: 2024

Journal Articles

An Artificial Intelligence-Based Federated Learning Platform to Boost Precision Medicine in Rare Hematological Diseases: An Initiative By GenoMed4all and Synthema Consortia

Gianluca Asti, Saverio D'Amico, Luciana Carota, Davide Piscia, Francesco Casadei, Nono Saha Cyrille Merleau, Patricia Alonso de Apellániz, Anne Sophie Kubasch, Silke Gloaguen, Nicole Modler, Catalina Gonzalez Martin, Cesare Rollo, Juan Parras, Mattia Delleani, Elena Zazzetti, Elisabetta Sauta, Nico Curti, Nicolas Riccardo Derus, Gianluca Carlini, Daniele Dall'Olio, Claudia Sala, Lorenzo Dall'Olio, Luca Lanino, Giulia Maggioni, Alessia Campagna, Marilena Bicchieri, Arturo Bonometti, Cesare Lancellotti, Daoud Rahal, Luca Di Tommaso, Tiziana Sanavia, Piero Fariselli, Matteo Zampini, Matteo Brindisi, Victor Savevski, Uwe Platzbecker, Maria Diez-Campelo, Lin Pierre Zhao, Pierre Fenaux, Torsten Haferlach, Vincent Planat, Raffaella Colombatti, Maria del Mar Mañú-Pereira, Anders Krogh, Silvia Uribe, Santiago Zazo, Enrico Giampieri, Gastone Castellani, Matteo Giovanni Della Porta, Federico Alvarez

Blood (2024) 144 (Supplement 1): 4989.

https://doi.org/10.1182/blood-2024-205541

Published: 2024

Journal Articles

Characterizing People with Sickle Cell Disease Who Share Attitudes Regarding Clinical Trial Participation: Findings from the Global LISTEN Survey

Johnny Mahlangu, John James, Biree Andemariam, John Waller, Samar Al-Behaisi, Gareth Morrell, Raffaella Colombatti, Cassandra Trimnell

Blood (2024) 144 (Supplement 1): 1135.

https://doi.org/10.1182/blood-2024-200550

Published: 2024

Journal Articles

Oxygen Gradient Ektacytometry Is Associated with Markers of Hemolysis and Inflammation in a Large Sickle Cell Disease Cohort within the GenoMed4ALL Project

Blood (2024) 144 (Supplement 1): 290.

https://doi.org/10.1182/blood-2024-200639

Published: 2024

Journal Articles

uRADAR: European Patients Referral Frame to Improve Access to New Drugs and Therapies in Ultra-Rare Anemia Disorders and Severe Hereditary Spherocytosis

Blood (2024) 144 (Supplement 1): 794.

https://doi.org/10.1182/blood-2024-201501

Published: 2024

Journal Articles

Data Driven Research through the European RADeep Registry and the Use of Artificial Intelligence Towards Personalized Medicine in Sickle Cell Disease

Blood (2024) 144 (Supplement 1): 1138.

https://doi.org/10.1182/blood-2024-203331

Published: 2024

Journal Articles

Motivators and Barriers for People with Sickle Cell Disease Participating in Clinical Trials: Global Findings from the LISTEN Survey

John James, Biree Andemariam, Johnny Mahlangu, Raffaella Colombatti, John Waller, Samar Al-Behaisi, Adam Wufsus, Gareth Morrell, Cassandra Trimnell

Blood (2023) 142 (Supplement 1): 2498.

https://doi.org/10.1182/blood-2023-181910

Published: 2023

Journal Articles

A Phase 2/3, Double-Blind, Randomized, Placebo-Controlled, Multicenter Study of Mitapivat in Patients with Sickle Cell Disease: RISE UP Phase 2 Results

Blood (2023) 142 (Supplement 1): 271.

https://doi.org/10.1182/blood-2023-187033

Published: 2023

Journal Articles

Cross-Community Collaboration and Data Collection to Optimize Patient Care in Hemolytic Anemias

Blood (2023) 142 (Supplement 1): 3692.

https://doi.org/10.1182/blood-2023-181632

Published: 2023

Journal Articles

The Areal Project: How Virtual Reality Application Could Enhance Patient's Quality Time during Transfusion Therapy in Adult Patients with Thalassemia and Sickle Cell Disease

Valentino Megale, Maddalena Casale, Raffaella Colombatti, Valeria Pinto, Ilaria Baido, Cristina Brentan, Gian Luca Forni, Miriam Forte, Barbara Gianesin, Francesca Grieco, Elizabeth Maran, Vania Munaretto, Silverio Perrotta, Maria Caterina Putti, Giacomo Robello

Blood (2022) 140 (Supplement 1): 13049–13050.

https://doi.org/10.1182/blood-2022-165189

Published: 2022

Journal Articles

Insights into Vaso-Occlusive Crises-Related Readmissions in Patients with SCD across Geographic Regions

Raffaella Colombatti, Carolyn Hoppe, Elliott P. Vichinsky, Mona Hamdy, Adeseye Michael Akinsete, Mark Davis, Halima Bello-Manga, Iheanyi Okpala, Ana Cristina Silva Pinto, Adlette Inati

Blood (2022) 140 (Supplement 1): 5453–5455.

https://doi.org/10.1182/blood-2022-167948

Published: 2022

Journal Articles

Limited Access to Transcranial Doppler Screening and Stroke Prevention for Children with Sickle Cell Disease in Europe: Results of a Multinational Eurobloodnet Survey

Daniela Cuzzubbo, Victoria Gutierrez-Valle, Maddalena Casale, Vincenzo Voi, Corrina McMahon, Maria Del Mar Mañú Pereira, Mariane de Montalembert, Baba PD Inusa, Raffaella Colombatti

Blood (2021) 138 (Supplement 1): 915.

https://doi.org/10.1182/blood-2021-147298

Published: 2021

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Thalassemia in europe: A cross-border real-world data analysis from the radeep registry

Bridging the gap: Global caregiver perspectives on awareness, motivators, and barriers to clinical trial participation in sickle cell disease

Qualitative interviews exploring the patient experience of fatigue in individuals with sickle cell disease (SCD), thalassemia, and pyruvate kinase (PK) deficiency

Data validation and quality framework for building a european multimodal real-world dataset for clinical outcome research in sickle cell disease

Sickle cell disease in europe: A cross-border real-world data analysis from the radeep registry

Patient-driven insights in sickle cell disease: Results from a global survey informing public health strategies

Implementing patient-centered PROMs in sickle cell disease care: A european consensus approach

Sickle cell disease trials redefined: Toward unified clinical endpoints through international consensus

How People with Sickle Cell Disease Rate Motivators is Associated with the Likelihood of Wanting to Participate in a Clinical Trial: Findings from the Global LISTEN Survey

An Artificial Intelligence-Based Federated Learning Platform to Boost Precision Medicine in Rare Hematological Diseases: An Initiative By GenoMed4all and Synthema Consortia

Characterizing People with Sickle Cell Disease Who Share Attitudes Regarding Clinical Trial Participation: Findings from the Global LISTEN Survey

Oxygen Gradient Ektacytometry Is Associated with Markers of Hemolysis and Inflammation in a Large Sickle Cell Disease Cohort within the GenoMed4ALL Project

uRADAR: European Patients Referral Frame to Improve Access to New Drugs and Therapies in Ultra-Rare Anemia Disorders and Severe Hereditary Spherocytosis

Data Driven Research through the European RADeep Registry and the Use of Artificial Intelligence Towards Personalized Medicine in Sickle Cell Disease

Motivators and Barriers for People with Sickle Cell Disease Participating in Clinical Trials: Global Findings from the LISTEN Survey

A Phase 2/3, Double-Blind, Randomized, Placebo-Controlled, Multicenter Study of Mitapivat in Patients with Sickle Cell Disease: RISE UP Phase 2 Results

Cross-Community Collaboration and Data Collection to Optimize Patient Care in Hemolytic Anemias

The Areal Project: How Virtual Reality Application Could Enhance Patient's Quality Time during Transfusion Therapy in Adult Patients with Thalassemia and Sickle Cell Disease

Insights into Vaso-Occlusive Crises-Related Readmissions in Patients with SCD across Geographic Regions

Limited Access to Transcranial Doppler Screening and Stroke Prevention for Children with Sickle Cell Disease in Europe: Results of a Multinational Eurobloodnet Survey

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