Julian Navarro-Sevilla
Nino Jesus, MD, Spain
Last Updated: 09/26/2026
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Found 8 publications
Next generation sequencing for diagnosis of hereditary anemia: Experience in a Spanish reference center.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 04, 2022
Survival and toxicity outcomes of hematopoietic stem cell transplantation for pediatric patients with Fanconi anemia: a unified multicentric national study from the Spanish Working Group for Bone Marrow Transplantation in Children.
Journal: Bone marrow transplantation
Published: May 24, 2020
Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.
Journal: International journal of laboratory hematology
Published: March 24, 2017
Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shortening.
Journal: Human molecular genetics
Published: January 12, 2017
Red cell pyruvate kinase deficiency in Spain: A study of 15 cases.
Journal: Medicina clinica
Published: June 02, 2016
Autoimmune cytopenias: diagnosis before treatment. Reply by the authors
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: July 16, 2013
Update on L-asparaginase treatment in paediatrics
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: March 04, 2013
Role of rituximab in the management of refractory autoimmune cytopenia
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: March 27, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026