Detalhe da pesquisa
1.
Haemoglobin Bristol-Alesha in a child with non-spherocytic severe haemolytic anaemia and marked anisochromic poikilocytosis with basophilic stippling and amorphous intracellular content.
Blood Cells Mol Dis
; 94: 102652, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35091138
2.
Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis.
Haematologica
; 105(2): 338-347, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31147440
3.
Meeting Report: The Equality Project on Endocrine Complications in Thalassemia: Selected Highlights from the First Turkish Congress, Antalya, 10th-11th December 2018.
Pediatr Endocrinol Rev
; 16(3): 401-411, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30888129
4.
Enzymatic and metabolic characterization of the phosphoglycerate kinase deficiency associated with chronic hemolytic anemia caused by the PGK-Barcelona mutation.
Blood Cells Mol Dis
; 46(3): 206-11, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21269848
5.
Epidemiology of rare anaemias in Europe.
Adv Exp Med Biol
; 686: 375-96, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20824457
6.
A comprehensive update of ICET-A Network on COVID-19 in thalassemias: what we know and where we stand.
Acta Biomed
; 91(3): e2020026, 2020 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32921722
7.
Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study.
Mediterr J Hematol Infect Dis
; 12(1): e2020046, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32670524
8.
Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
Hemoglobin
; 33(3): 226-34, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19657837
9.
Thyroid Disorders in Homozygous ß-Thalassemia: Current Knowledge, Emerging Issues and Open Problems.
Mediterr J Hematol Infect Dis
; 11(1): e2019029, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31205633
10.
The EHA Research Roadmap: Normal Hematopoiesis.
Hemasphere
; 5(12): e669, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34853826
11.
Phosphoglycerate mutase BB isoenzyme deficiency in a patient with non-spherocytic anemia: familial and metabolic studies.
Haematologica
; 90(2): 257-9, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15710582
12.
Haemoglobinopathies in Europe: health & migration policy perspectives.
Orphanet J Rare Dis
; 9: 97, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24980780
13.
Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.
Blood
; 102(1): 353-6, 2003 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12649162