Detalhe da pesquisa
1.
Pediatric Acute B-Cell Lymphoblastic Leukemia Developing Following Recent SARS-CoV-2 Infection.
J Pediatr Hematol Oncol
; 43(8): e1177-e1180, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33480653
2.
Long-term follow-up of children with risk organ-negative Langerhans cell histiocytosis after 2-chlorodeoxyadenosine treatment.
Br J Haematol
; 191(5): 825-834, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32700439
3.
Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.
Haematologica
; 104(8): 1554-1564, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30655378
4.
Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients.
Haematologica
; 103(8): 1278-1287, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29724903
5.
Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome.
Pediatr Dermatol
; 35(6): e375-e377, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30189467
6.
Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation.
Blood Cells Mol Dis
; 66: 11-18, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28772256
7.
The RELIVE consortium for relapsed or refractory pediatric hepatoblastoma and hepatocellular carcinoma: a scoping review of the problem and a proposed solution.
EClinicalMedicine
; 69: 102446, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38384339
8.
Molecular mechanisms of the defective hepcidin inhibition in TMPRSS6 mutations associated with iron-refractory iron deficiency anemia.
Blood
; 113(22): 5605-8, 2009 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19357398
9.
Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescents.
Joint Bone Spine
; 70(2): 149-53, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12713862
10.
Tufted angioma with Kasabach-Merritt syndrome mistaken for child abuse.
Forensic Sci Int
; 245: e15-7, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25459275
11.
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.
Nat Commun
; 4: 1884, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23695678