Detalhe da pesquisa
1.
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis.
Eur J Haematol
; 113(1): 82-89, 2024 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-38556258
2.
Changing Disease Course of Crimean-Congo Hemorrhagic Fever in Children, Turkey.
Emerg Infect Dis
; 29(2): 268-277, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36692327
3.
Intestinal mycobiota composition and changes in children with thalassemia who underwent allogeneic hematopoietic stem cell transplantation.
Pediatr Blood Cancer
; 69(1): e29411, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34699120
4.
Liposomal amphotericin B related late-onset hyperphosphatemia in a pediatric patient with acute myeloid leukemia.
J Oncol Pharm Pract
; 28(6): 1478-1482, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-35102765
5.
Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia.
Pediatr Transplant
; 25(5): e13942, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-33320995
6.
Genome instability is a consequence of transcription deficiency in patients with bone marrow failure harboring biallelic ERCC6L2 variants.
Proc Natl Acad Sci U S A
; 115(30): 7777-7782, 2018 07 24.
Artigo
Inglês
| MEDLINE | ID: mdl-29987015
7.
Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patients.
Pediatr Blood Cancer
; 67(12): e28722, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32970355
8.
Hb H Disease Diagnosed During Adolescent Pregnancy.
Hemoglobin
; 44(2): 137-138, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-32400222
9.
A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat.
J Pediatr Hematol Oncol
; 40(7): e458-e460, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-29309376
10.
Two versus three day upfront use of granulocyte-colony stimulating factor in healthy bone marrow donors for pediatric bone marrow transplantation.
Transfus Apher Sci
; 56(6): 829-831, 2017 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-29153311
11.
Hemophagocytosis in bone marrow aspirates in multisystem inflammatory syndrome in children.
Pediatr Blood Cancer
; 68(6): e28931, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33619863
12.
Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.
Blood
; 132(12): 1349-1353, 2018 09 20.
Artigo
Inglês
| MEDLINE | ID: mdl-30064976
13.
Comment on: Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21.
Pediatr Blood Cancer
; 67(11): e28289, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32725847
14.
Secondary antifungal prophylaxis in pediatric hematopoietic stem cell transplants.
J Pediatr Hematol Oncol
; 37(1): e19-22, 2015 01.
Artigo
Inglês
| MEDLINE | ID: mdl-25522351
15.
Massive splenic infarction and portal vein thrombosis in children with chronic myeloid leukemia.
J Pediatr Hematol Oncol
; 36(7): e471-2, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-24942025
16.
Use of plerixafor for peripheral blood stem cell mobilization failure in children.
Transfus Apher Sci
; 50(2): 214-8, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24512717
17.
Homozygosity for HBA1: c.179G > A: Hb Adana in an infant.
Hemoglobin
; 38(6): 449-50, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25342395
18.
Iron Deficiency Anemia in Infancy, Childhood, and Adolescence.
Turk Arch Pediatr
; 58(4): 358-362, 2023 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-37357449
19.
A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia.
Turk J Pediatr
; 65(1): 124-128, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36866992
20.
Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient.
Turk J Pediatr
; 65(5): 874-880, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37853979