Detalhe da pesquisa
1.
Poverty and relapse risk in children with acute lymphoblastic leukemia: a Children's Oncology Group study AALL03N1 report.
Blood
; 142(3): 221-229, 2023 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37070673
2.
Defective monocyte plasticity and altered cAMP pathway characterize USB1-mutated poikiloderma with neutropenia Clericuzio type.
Br J Haematol
; 204(2): 683-693, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37779259
3.
Body mass index during maintenance therapy and relapse risk in children with acute lymphoblastic leukemia: A Children's Oncology Group report.
Cancer
; 129(1): 151-160, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36369905
4.
Duffy-Null Phenotype-Associated Neutropenia is the Most Common Etiology for Leukopenia/Neutropenia Referrals to a Tertiary Children's Hospital.
J Pediatr
; 262: 113608, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37419240
5.
Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency.
N Engl J Med
; 381(10): 933-944, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31483964
6.
The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency.
Br J Haematol
; 192(6): 1092-1096, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32463523
7.
Aberrant myelomonocytic CD56 expression in Down syndrome is frequent and not associated with leukemogenesis.
Ann Hematol
; 100(7): 1695-1700, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33890142
8.
Pyruvate kinase deficiency in children.
Pediatr Blood Cancer
; 68(9): e29148, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34125488
9.
Patterns and correlates of preserved humoral immunity to vaccines in children following allogeneic hematopoietic stem cell transplantation.
Pediatr Transplant
; 25(5): e13936, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33326673
10.
Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin.
Pediatr Hematol Oncol
; 38(1): 65-79, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32990483
11.
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.
Blood
; 131(20): 2183-2192, 2018 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29549173
12.
Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.
Am J Hematol
; 95(5): 472-482, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32043619
13.
CD14/16 monocyte profiling in juvenile myelomonocytic leukemia.
Pediatr Blood Cancer
; 67(9): e28555, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32648963
14.
Successful Treatment of an Adolescent Male With Severe Refractory Evans Syndrome Using Bortezomib-based Therapy.
J Pediatr Hematol Oncol
; 42(2): e110-e113, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30299351
15.
Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia.
Pediatr Blood Cancer
; 71(6): e30955, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38523248
16.
Role of Initiating Supportive Care Preceding Veno-occlusive Disease Diagnosis Following Allogeneic Hematopoietic Stem Cell Transplantation in Children.
J Pediatr Hematol Oncol
; 41(6): e395-e401, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30933024
17.
Acquired Pure Red Cell Aplasia and Acquired Amegakaryocytic Thrombocytopenia Associated With Clonal Expansion of T-Cell Large Granular Lymphocytes in a Patient With Lipopolysaccharide-responsive Beige-like Anchor (LRBA) Protein Deficiency.
J Pediatr Hematol Oncol
; 41(8): e542-e545, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30188351
18.
Identification of a novel variant in phosphoglycerate kinase-1 (PGK1) in an African-American child (PGK1 Detroit).
Pediatr Hematol Oncol
; 36(5): 302-308, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31424298
19.
Mild erythrocytosis as a presenting manifestation of PIEZO1 associated erythrocyte volume disorders.
Pediatr Hematol Oncol
; 36(5): 317-326, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31298594
20.
Germline mutations as potential causes of childhood solid tumours: comments on the Norwegian childhood cancer cohort study.
Br J Cancer
; 118(8): 1033-1034, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29593336