Detalhe da pesquisa
1.
Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia.
Blood Cells Mol Dis
; 83: 102436, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32434137
2.
Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia.
Ann Hematol
; 98(12): 2673-2681, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31478061
3.
Comparison of outcomes of immunosuppressive therapy with rabbit versus horse antithymocyte globulin and cyclosporine a in children with acquired severe aplastic anemia.
Am J Hematol
; 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38622880
4.
Sickle Cell Disease Diagnosis Uncovered by Incidental Radiograph Findings.
J Pediatr Hematol Oncol
; 45(3): 151, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36730969
5.
Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.
Ann Hematol
; 96(11): 1921-1929, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28887661
6.
Pantoea Species Bacteremia in a Child With Sickle Cell Disease: Looking for a Culprit.
J Pediatr Hematol Oncol
; 39(6): e307-e308, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28267078
7.
Prolonged thrombocytopenia in a child with severe neonatal alloimmune reaction and Noonan syndrome.
Platelets
; 27(4): 381-2, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26599469
8.
Osteoarticular infections in paediatric sickle cell disease: in the era of multidrugresistant bacteria.
Br J Haematol
; 189(4): e147-e150, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32150291
9.
Refractory immune hemolytic anemia in an immunocompetent infant with cytomegalovirus infection.
Pediatr Blood Cancer
; 66(8): e27791, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31045313
10.
Cold Agglutinin Syndrome and Hemophagocytic Lymphohistiocytosis: An Unusual Combination Caused by Epstein-Barr Virus Infection.
Cureus
; 16(1): e52179, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38344610
11.
Cutaneous hyperpigmentation and cobalamin deficiency.
Br J Haematol
; 174(6): 834, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27433789
12.
Linezolid in the treatment of multidrug-resistant/extensively drug-resistant tuberculosis in paediatric patients: experience of a paediatric infectious diseases unit.
Scand J Infect Dis
; 43(6-7): 556-9, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21391771
13.
Eltrombopag Use in Children with Persistent and Chronic Primary Immune Thrombocytopenia in a Portuguese Pediatric Center.
Acta Med Port
; 37(4): 294-295, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38631059
14.
Haemophilia A: health and economic burden of a rare disease in Portugal.
Orphanet J Rare Dis
; 14(1): 211, 2019 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31484564
15.
Spontaneous neonatal humeral artery thromboembolism: a case report.
BMJ Case Rep
; 14(4)2021 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33910793
16.
Sickle cell anemia - Nitric oxide related genetic modifiers of hematological and biochemical parameters.
Clin Hemorheol Microcirc
; 64(4): 957-963, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27802215
17.
Hemorheological alterations in sickle cell anemia and their clinical consequences - The role of genetic modulators.
Clin Hemorheol Microcirc
; 64(4): 859-866, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27814292
18.
Genotype-phenotype correlation in a cohort of Portuguese patients comprising the entire spectrum of VWD types: impact of NGS.
Thromb Haemost
; 116(1): 17-31, 2016 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26988807
19.
Retinopathy and bone marrow failure revealing Coats plus syndrome.
BMJ Case Rep
; 20182018 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29523622