Detalhe da pesquisa
1.
NOVEL THERAPEUTIC APPROACHES IN THALASSEMIAS, SICKLE CELL DISEASE AND OTHER RED CELL DISORDERS.
Blood
; 2024 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-38820588
2.
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group.
Br J Haematol
; 204(1): 306-314, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37990447
3.
Reduction of extramedullary erythropoiesis and amelioration of anemia in a ß-thalassemia patient treated with thalidomide.
Am J Hematol
; 99(3): 463-464, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38146593
4.
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021.
Cancer
; 129(1): 107-117, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36321594
5.
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
Am J Hematol
; 98(6): E130-E133, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36882369
6.
Overall and complication-free survival in a large cohort of patients with ß-thalassemia major followed over 50 years.
Am J Hematol
; 98(3): 381-387, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36588408
7.
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry.
J Cell Mol Med
; 26(9): 2520-2528, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35355397
8.
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values.
Ann Hematol
; 99(9): 2047-2055, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32691114
9.
Management of Iron Overload in Beta-Thalassemia Patients: Clinical Practice Update Based on Case Series.
Int J Mol Sci
; 21(22)2020 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33233561
10.
Mortality in ß-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization.
Blood
; 139(13): 2080-2083, 2022 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34986266
11.
Premature aging of the immune system affects the response to SARS-CoV-2 mRNA vaccine in ß-thalassemia: role of an additional dose.
Blood
; 140(15): 1735-1738, 2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36004936
12.
Reply to "Hepatocellular carcinoma in thalassemia and other hemoglobinopathies".
Cancer
; 129(10): 1616-1617, 2023 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917138
13.
Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from three decades of follow-up in a high-income setting.
Haematologica
; 108(4): 1158-1162, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35924578
14.
Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients.
Am J Hematol
; 98(6): E145-E147, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36871203
15.
Tricuspid-valve regurgitant jet velocity as a risk factor for death in ß-thalassemia.
Haematologica
; 107(7): 1714-1718, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35236055
16.
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection.
Am J Hematol
; 97(2): E75-E78, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34861054
17.
Comparison between different software programs and post-processing techniques for the MRI quantification of liver iron concentration in thalassemia patients.
Radiol Med
; 121(10): 751-62, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27334009
18.
Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease.
Orphanet J Rare Dis
; 19(1): 22, 2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38254184
19.
Lack of correlation between heart, liver and pancreas MRI-R2*: Results from long-term follow-up in a cohort of adult ß-thalassemia major patients.
Am J Hematol
; 93(3): E79-E82, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29265491
20.
Daily alternating deferasirox and deferiprone therapy successfully controls iron accumulation in untreatable transfusion-dependent thalassemia patients.
Am J Hematol
; 93(10): E338-E340, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30033633