Detalhe da pesquisa
1.
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections.
Int Arch Allergy Immunol
; 185(4): 392-401, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154455
2.
HAX1-related congenital neutropenia: Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR).
Br J Haematol
; 202(2): 393-411, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37193639
3.
Family Knowledge, Attitudes, and Practices Toward Severe Congenital Neutropenia.
J Pediatr Hematol Oncol
; 45(4): e441-e445, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36897312
4.
A rare complication of leukostasis with AML M4 patient: Microcirculatory dysfunction of upper extremities.
Transfus Apher Sci
; 62(4): 103717, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37173209
5.
Clinical features and prognostic factors of Magnusiomyces (Saprochaete) infections in haematology. A multicentre study of SEIFEM/Fungiscope.
Mycoses
; 66(1): 35-46, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36064299
6.
A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia.
J Pediatr Hematol Oncol
; 43(6): e780-e784, 2021 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33843817
7.
Management of a Patient With Congenital Biallelic CSF3R Mutation With GM-CSF.
J Pediatr Hematol Oncol
; 42(3): e164-e166, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30499904
8.
COVID-19 disease in patients with chronic neutropenia: The experience from the European Network for Innovative Diagnosis and Treatment of Chronic Neutropenias.
Br J Haematol
; 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38506338
9.
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Pediatr Blood Cancer
; 66(10): e27923, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31321910
10.
Congenital Neutropenia Patient With Hypomorphic Biallelic CSF3R Mutation Responding to GCSF.
J Pediatr Hematol Oncol
; 41(3): e190-e192, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30028820
11.
Hepatosplenic Fungal Infections in Children With Leukemia-Risk Factors and Outcome: A Multicentric Study.
J Pediatr Hematol Oncol
; 41(4): 256-260, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30730381
12.
HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.
Br J Haematol
; 177(4): 597-600, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28169428
13.
Inferior Petrosal Sinus Thrombosis in a Child due to Malposition of Central Venous Catheter: A Case Report.
Med Princ Pract
; 26(6): 579-581, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29080892
14.
Proven and probable invasive fungal infections in children with acute lymphoblastic leukaemia: results from an university hospital, 2005-2013.
Mycoses
; 58(4): 225-32, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25728069
15.
Therapeutic plasma exchange in critically ill children: A single center experience.
Ther Apher Dial
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747186
16.
Aplastic Anemia Frequency and Management in Pediatric Liver Transplantations Due to Non-A-E Hepatitis.
Turk J Gastroenterol
; 32(3): 313-317, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34160361
17.
Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group.
Turk J Haematol
; 27(4): 257-62, 2010 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27263739
18.
Fertility in Patients with Thalassemia and Outcome of Pregnancies: A Turkish Experience
Turk J Haematol
; 36(4): 274-277, 2019 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31198015
19.
Diagnostic Accuracy of Serum Galactomannan Assay in Children with Acute Myeloid Leukemia: Effect of the Revised EORTC/MSGERC 2020 Criteria
Turk J Haematol
; 40(4): 278-280, 2023 12 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37791618
20.
Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome.
JMM Case Rep
; 5(10): e005167, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30479781