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Fernando Pinto

Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling
2013 · Franco Locatelli, Nabil Kabbara, et al. · Blood · 244
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
2020 · James E. D. Thaventhiran, Hana Lango Allen, et al. · Nature · 240
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Primary leptomeningeal lymphoma
2013 · Jennie W. Taylor, Eoin P. Flanagan, et al. · Neurology · 99
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Use of the complement inhibitor Coversin to treat HSCT-associated TMA
2017 · Timothy H. J. Goodship, Fernando Pinto, et al. · Blood Advances · 44
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Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
2023 · Maria Elena Maccari, Pascal Schneider, et al. · Journal of Allergy and Clinical Immunology · 18
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Current practice and registration patterns among United Kingdom Haemophilia Centre Doctors’ Organisation centers for patients with unclassified bleeding disorders
2021 · Will Thomas, Kate Downes, et al. · Journal of Thrombosis and Haemostasis · 15
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Factor VIII genotype and the risk of developing high-responding or low-responding inhibitors in severe hemophilia A: data from the PedNet Hemophilia Cohort of 1,202 children
2023 · Nadine G. Andersson, Veerle Labarque, et al. · Haematologica · 6
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Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort
2020 · James E. D. Thaventhiran, Hana Lango Allen, et al. · Nature · 6
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Hemophilia B Leyden: characteristics and natural history in the International Pediatric Network of Hemophilia Management Registry
2024 · Mutlu Kartal-Kaess, Fernando Pinto, et al. · Journal of Thrombosis and Haemostasis · 3
Infantile acute liver failure in the West of Scotland
2019 · David Wands, Rachel Tayler, et al. · Archives of Disease in Childhood · 2
Apixaban for the treatment of venous thromboembolic events in paediatric patients: an open-label, multicentre, randomised, controlled descriptive trial
2026 · Leonardo R Brandão, Leonardo R Brandão, et al. · The Lancet Haematology · 1
Inhibitor development according to FVIII concentrates in previously untreated patients with severe hemophilia A: update from the PedNet registry
2026 · Kathelijn Fischer, Martin Olivieri, et al. · Journal of Thrombosis and Haemostasis · 1
PB2249 18-year experience of a Scotland-wide and exclusively Point-Of-Care (POC) and home-monitoring-based Anticoagulation Service for children receiving long term Warfarin
2026 · Calum Sampson, Katrina Adams, et al. · Research and Practice in Thrombosis and Haemostasis
PB2271 Head bleeds in hemophilia in the first three months of life – insights from the PedNet registry
2026 · Ester Zapotocka, Marloes de Kovel, et al. · Research and Practice in Thrombosis and Haemostasis
Review of transfusion practice for beta thalassaemia major patients in Scotland after removal of age criteria for red cell transfusion
2025 · Nicole Priddee, Katie Hands, et al. · Transfusion Medicine
Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)
2020 · Hana Lango Allen, William Rae, et al. · Newcastle University ePrints (Newcastle Univesity)
A Prospective Study on the Feasibility of Related and Unrelated Donor Search and Hematopoietic Cell Transplantation for Adults with Acute Leukemia at 31 European Transplant Centers
2008 · Vanderson Rocha, Mutlu Arat, et al. · Blood
Inhibitor development according to FVIII concentrates in PUPs with severe hemophilia A: update from the PedNet registry.
· Fischer, Kathelijn, Olivieri, Martin, et al. · Open Access CRIS of the University of Bern
Works count: 20
Citation count: 679
H-index: 6
I10-index: 6
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