Detalhe da pesquisa
1.
Germline bi-allelic SH2B3/LNK alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder.
Haematologica
; 2023 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981895
2.
Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies.
Blood Cells Mol Dis
; 79: 102342, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31302454
3.
Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy.
Ann Hum Biol
; 46(7-8): 610-615, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31793346
4.
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).
J Clin Immunol
; 35(8): 745-53, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26464197
5.
Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease.
Ann Hematol
; 97(11): 2261-2262, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754272
6.
Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report.
J Clin Immunol
; 36(5): 437-40, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27146824