Found: 8
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Southeast Asian ovalocytosis detected in a critical patient with COVID‐19 pneumonia.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 11, p. E416, doi. 10.1002/ajh.26323
- By:
- Publication type:
- Article
Red Cell Properties after Different Modes of Blood Transportation.
- Published in:
- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2016.00288
- By:
- Publication type:
- Article
Recommendations for centres of expertise in rare anaemias. The ENERCA White Book.
- Published in:
- Thalassemia Reports, 2014, v. 4, n. 3, p. 86, doi. 10.4081/thal.2014.4878
- By:
- Publication type:
- Article
e-ENERCA: telemedicine platform for rare anaemias.
- Published in:
- Thalassemia Reports, 2014, v. 4, n. 3, p. 91, doi. 10.4081/thal.2014.4879
- By:
- Publication type:
- Article
Pathophysiology of Anemia in HIV-Infected Children Exposed to Malaria.
- Published in:
- American Journal of Tropical Medicine & Hygiene, 2021, v. 104, n. 3, p. 1003, doi. 10.4269/ajtmh.19-0783
- By:
- Publication type:
- Article
Low affinity hemoglobinopathy ( Hb Vigo) due to a new mutation of beta globin gene (c200 A> T; Lys> Ile). A cause of rare anemia misdiagnosis.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 4, p. E38, doi. 10.1002/ajh.24649
- By:
- Publication type:
- Article
Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 12, p. E217, doi. 10.1002/ajh.24178
- By:
- Publication type:
- Article