Works by Vagace, Jose
Results: 12
Etiopathological mechanisms and clinical characteristics of hyperhemolysis syndrome in Spanish patients with thalassemia.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Phase 2 Clinical Trial of Infusing Haploidentical K562-mb15-41BBL–Activated and Expanded Natural Killer Cells as Consolidation Therapy for Pediatric Acute Myeloblastic Leukemia.
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2021, v. 21, n. 5, p. 328, doi. 10.1016/j.clml.2021.01.013
- By:
- Publication type:
- Article
Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3.
- Published in:
- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 3, p. 221, doi. 10.1002/mgg3.136
- By:
- Publication type:
- Article
Methotrexate-induced subacute neurotoxicity in a child with acute lymphoblastic leukemia carrying genetic polymorphisms related to folate homeostasis.
- Published in:
- American Journal of Hematology, 2011, v. 86, n. 1, p. 98, doi. 10.1002/ajh.21897
- By:
- Publication type:
- Article
Aplastic anemia during treatment with albendazole.
- Published in:
- American Journal of Hematology, 1996, v. 53, n. 1, p. 53, doi. 10.1002/1096-8652(199609)53:1<53::AID-AJH2830530104>3.0.CO;2-Q
- By:
- Publication type:
- Article
Expanding the Clinical and Genetic Spectra of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected and Unexpected Findings.
- Published in:
- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.02325
- By:
- Publication type:
- Article
Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Hyperhaemolysis syndrome responsive to splenectomy in a patient with δβ-thalassaemia: a discussion on underlying mechanisms
- Published in:
- Blood Transfusion (17232007), 2014, v. 12, n. 1, p. 127, doi. 10.2450/2013.0059-13
- By:
- Publication type:
- Article
Thalassemia diagnosis in a blood donor from a unique trimorphic red blood cell population observed in the recipient.
- Published in:
- 2014
- By:
- Publication type:
- Letter to the Editor
Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report.
- Published in:
- BMC Infectious Diseases, 2007, v. 7, n. 1, p. 40, doi. 10.1186/1471-2334-7-40
- By:
- Publication type:
- Article