Detalhe da pesquisa
1.
Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3.
Br J Haematol
; 203(4): 678-683, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37646304
2.
Dominant inherited ß-thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB.
Pediatr Blood Cancer
; 70(10): e30511, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37353956
3.
Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor.
Front Immunol
; 13: 869047, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35812385
4.
Occurrence of autoimmune pancreatitis after chronic immune thrombocytopenia in a Caucasian adolescent.
Clin J Gastroenterol
; 14(3): 918-922, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33743140
5.
A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.
Hemasphere
; 8(1): e31, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38434532