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
Works by Vagace, Jose Manuel
Results: 8
1
2
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
3
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
4
Etiopathological mechanisms and clinical characteristics of hyperhemolysis syndrome in Spanish patients with thalassemia.
- Published in:
- 2016
- By:
- Publication type:
- journal article
5
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
6
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
7
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
8
Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene.
- Published in:
- 2022
- By:
- Publication type:
- Case Study