Detalhe da pesquisa
1.
Characteristics of patients with C1 esterase inhibitor deficiency: a single center study.
Eur Ann Allergy Clin Immunol
; 53(2): 75-79, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32351099
2.
Primary Immunodeficiency Disorders in children with Non-Cystic Fibrosis Bronchiectasis.
Eur Ann Allergy Clin Immunol
; 52(6): 271-276, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32372587
3.
Clinical and genetic features of the patients with X-Linked agammaglobulinemia from Turkey: Single-centre experience.
Scand J Immunol
; 87(3)2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29424453
4.
Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing.
Scand J Immunol
; 85(3): 227-234, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28109013
5.
Bone marrow transplantation with Favorable outcome in three patients with LPS-responsive beige-like anchor (LRBA) deficiency.
Clin Immunol
; 203: 162-165, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31026575
6.
A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma.
J Investig Allergol Clin Immunol
; 28(4): 271-273, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30073964
7.
Association of interleukin-1 beta (+3954) gene polymorphism and gingival crevicular fluid levels in patients with aggressive and chronic periodontitis.
Genet Couns
; 24(1): 21-35, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23610862
8.
Naturally acquired hepatitis A antibodies after haematopoetic stem cell transplantation.
Epidemiol Infect
; 139(5): 683-7, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20619071
9.
Cernunnos deficiency: a case report.
J Investig Allergol Clin Immunol
; 21(4): 313-6, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21721379
10.
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.
Eur J Clin Invest
; 39(4): 311-9, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19292887
11.
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations.
Eur J Clin Invest
; 39(10): 942-51, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19624736
12.
Life-threatening neurological complications after bone marrow transplantation in children.
Bone Marrow Transplant
; 35(1): 71-6, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15531898
13.
Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia.
Hum Mutat
; 18(4): 356, 2001 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11668622
14.
High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from ataxia-telangiectasia patients.
Int J Radiat Oncol Biol Phys
; 49(2): 555-9, 2001 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11173154
15.
Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement.
Bone Marrow Transplant
; 24(8): 931-3, 1999 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-10516709
16.
Effects of intravenous immunoglobulin on clinical and immunological findings of patients with humoral immunodeficiency diseases.
Turk J Pediatr
; 34(4): 203-9, 1992.
Artigo
em Inglês
| MEDLINE | ID: mdl-1306339
17.
IgG subclasses in symptomatic IgA deficiency.
Turk J Pediatr
; 34(1): 1-4, 1992.
Artigo
em Inglês
| MEDLINE | ID: mdl-1509524
18.
Clinical and immunological aspects of hyper-IgM syndrome.
Turk J Pediatr
; 32(1): 13-20, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2288014
19.
Serum IgD concentrations in immunodeficiency diseases.
Turk J Pediatr
; 32(3): 175-82, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2093253
20.
Allogeneic bone marrow transplantation for children with myelodysplastic syndrome.
Turk J Pediatr
; 42(3): 192-7, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11105616