Detalhe da pesquisa
1.
Assessment of Ecotropic Viral Integration Site 2B (EVI2B) Gene in Juvenile Myelomonocytic Leukemia and Neurofibromatosis Type 1 NF1 Tumors.
Biochem Genet
; 62(2): 1263-1276, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-37584733
2.
Is Posaconazole Really Effective in Adolescent patients as a Prophylactic Agent: Experience of a Tertiary Care Center.
J Pediatr Hematol Oncol
; 43(5): e613-e618, 2021 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33560081
3.
Comparison of ferrous sulfate, polymaltose complex and iron-zinc in iron deficiency anemia.
Minerva Pediatr
; 71(5): 449-454, 2019 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26200522
4.
The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience.
Haematologica
; 103(2): 231-236, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29146706
5.
Hematopoietic Stem Cell Transplantation Using Preimplantation Genetic Diagnosis and Human Leukocyte Antigen Typing for Human Leukocyte Antigen-Matched Sibling Donor: A Turkish Multicenter Study.
Biol Blood Marrow Transplant
; 23(5): 790-794, 2017 May.
Artigo
Inglês
| MEDLINE | ID: mdl-28192253
6.
Hematopoietic stem cell transplantation in children with Griscelli syndrome: A single-center experience.
Pediatr Transplant
; 21(7)2017 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-28836324
7.
Magnetic resonance imaging of pulmonary infection in immunocompromised children: comparison with multidetector computed tomography.
Pediatr Radiol
; 47(2): 146-153, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-27796469
8.
Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey.
Pediatr Blood Cancer
; 63(4): 695-700, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26703084
9.
Severe Hypercalcemia in a Child With Acute Lymphoblastic Leukemia Relapse: Successful Management With Combination of Calcitonin and Bisphosphonate.
J Pediatr Hematol Oncol
; 38(3): 232-4, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26907650
10.
Hypereosinophilic Syndrome: Hacettepe Experience.
J Pediatr Hematol Oncol
; 38(7): 539-43, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27548336
11.
Sorafenib-induced Posterior Reversible Encephalopathy Syndrome in a Child With FLT3-ITD-positive Acute Myeloid Leukemia.
J Pediatr Hematol Oncol
; 38(3): 240-2, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26907662
12.
Macrophage activation syndrome in children with systemic juvenile idiopathic arthritis and systemic lupus erythematosus.
Rheumatol Int
; 36(10): 1421-9, 2016 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-27510530
13.
Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with ß-thalassemia major.
Ann Hematol
; 94(7): 1099-104, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25740381
14.
Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience.
Clin Exp Nephrol
; 19(3): 506-13, 2015 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24993948
15.
Basal cell carcinoma after treatment of childhood acute lymphoblastic leukemia and concise review of the literature.
Pediatr Dermatol
; 32(3): e82-5, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25781207
16.
Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant.
Turk J Haematol
; 32(1): 64-7, 2015 Mar 05.
Artigo
Inglês
| MEDLINE | ID: mdl-25805677
17.
A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.
Pediatr Blood Cancer
; 61(4): 763-4, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24115609
18.
Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesis.
Pediatr Blood Cancer
; 61(2): 302-5, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24106199
19.
Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II.
Pediatr Transplant
; 18(4): E130-3, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24724984
20.
Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis.
J Pediatr Hematol Oncol
; 35(5): e205-8, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23274377