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Pediatric Transplantation|August 1, 2007
Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantationJosu de la Fuente, Inderjeet Dokal
Transfusion|April 1, 2008
Hyperhemolysis syndrome in sickle cell disease: case report (recurrent episode) and literature reviewNay Win, Helen New, Edmond Lee, et al.
Hematology/Oncology and Stem Cell Therapy|March 24, 2020
Haploidentical bone marrow transplant with posttransplant cyclophosphamide for sickle cell disease: An updateDilan A Patel, Adeseye M Akinsete, Josu de la Fuente, et al.
Hematology/Oncology and Stem Cell Therapy|March 24, 2020
Alternative donor hematopoietic stem cell transplantation for sickle cell disease in EuropeEliane Gluckman, Barbara Cappelli, Graziana Maria Scigliuolo, et al.
The Lancet. Haematology|November 26, 2020
The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editingJosu de la Fuente, Eliane Gluckman, Julie Makani, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 8, 2024
Autologous gene therapy for hemoglobinopathies: From bench to patient's bedsideFranco Locatelli, Marina Cavazzana, Haydar Frangoul, et al.
The Journal of Gene Medicine|March 5, 2014
Nuclease-stimulated homologous recombination at the human β-globin geneTommaso Vannocci, Hitoshi Kurata, Josu de la Fuente, et al.
Haematologica|August 29, 2015
Impairment of neutrophil oxidative burst in children with sickle cell disease is associated with heme oxygenase-1Ceri Evans, Katharine Orf, Erzsebet Horvath, et al.
British Journal of Haematology|July 1, 2014
Managing children with chronic myeloid leukaemia (CML): recommendations for the management of CML in children and young people up to the age of 18 yearsJosu de la Fuente, André Baruchel, Andrea Biondi, et al.
Stem Cells (Dayton, Ohio)|December 31, 2004
Human fetal mesenchymal stem cells as vehicles for gene deliveryJerry Chan, Keelin O'Donoghue, Josu de la Fuente, et al.
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