Lista de obras -

A Rare Case of Primary Cerebral Hydatid Cyst

A case of oculoglandular tularemia resistant to medical treatment.

artículo científico publicado en 2013

A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from Turkey.

artículo científico publicado en 2017

A prospective study of etiology of childhood acute bacterial meningitis, Turkey.

artículo científico publicado en 2008

A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo

artículo científico publicado en 2008

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

artículo científico publicado en 2011

Bilateral intraocular calcification in necrotizing cytomegalovirus retinitis

artículo científico publicado en 2014

Chronic recurrent multifocal osteomyelitis: a rare skeletal disorder

artículo científico publicado en 2015

Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency

artículo científico publicado en 2010

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

artículo científico publicado en 2009

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.

artículo científico publicado en 2016

Evaluation of ppd response in patients with idiopathic arthritis who are on biological drug therapy.

artículo científico publicado en 2014

Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

artículo científico publicado en 2016

HHV-8-associated Kaposi sarcoma in a child with IFNgammaR1 deficiency

artículo científico publicado en 2004

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

artículo científico publicado en 2016

House Dust Mites Confer a Distinct Immunological Feature among Dermatitis

artículo científico publicado en 2016

IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

artículo científico publicado en 2011

IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans

artículo científico publicado en 2008

IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients

artículo científico publicado en 2012

Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis

artículo científico publicado en 2015

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

artículo científico publicado en 2015

Meningitis caused by Neisseria Meningitidis, Hemophilus Influenzae Type B and Streptococcus Pneumoniae during 2005-2012 in Turkey. A multicenter prospective surveillance study

artículo científico publicado en 2014

Multiple pericardial abscesses in a child with known chronic granulomatous disease

artículo científico publicado en 2016

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

artículo científico publicado en 2008

Primary diffuse leptomeningeal gliomatosis mimicking tuberculous meningitis

artículo científico publicado en 2013

Pyogenic bacterial infections in humans with MyD88 deficiency

artículo científico publicado en 2008

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

artículo científico publicado en 2010

Serotypes of Streptococcus pneumoniae isolates from children with invasive pneumococcal disease in Turkey: baseline evaluation of the introduction of the pneumococcal conjugate vaccine nationwide.

artículo científico publicado en 2011

Systemic lupus erythematosus due to Epstein-Barr virus or Epstein-Barr virus infection provocating acute exacerbation of systemic lupus erythematosus?

artículo científico publicado en 2005

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

artículo científico publicado en 2015

Tuberculin skin test response in patients with juvenile idiopathic arthritis on anti-TNF therapy

artículo científico publicado en 2018

Lista de obras de

A Rare Case of Primary Cerebral Hydatid Cyst

A case of oculoglandular tularemia resistant to medical treatment.

A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from Turkey.

A prospective study of etiology of childhood acute bacterial meningitis, Turkey.

A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

Bilateral intraocular calcification in necrotizing cytomegalovirus retinitis

Chronic recurrent multifocal osteomyelitis: a rare skeletal disorder

Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.

Evaluation of ppd response in patients with idiopathic arthritis who are on biological drug therapy.

Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

HHV-8-associated Kaposi sarcoma in a child with IFNgammaR1 deficiency

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

House Dust Mites Confer a Distinct Immunological Feature among Dermatitis

IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans

IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients

Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

Meningitis caused by Neisseria Meningitidis, Hemophilus Influenzae Type B and Streptococcus Pneumoniae during 2005-2012 in Turkey. A multicenter prospective surveillance study

Multiple pericardial abscesses in a child with known chronic granulomatous disease

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

Primary diffuse leptomeningeal gliomatosis mimicking tuberculous meningitis

Pyogenic bacterial infections in humans with MyD88 deficiency

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Serotypes of Streptococcus pneumoniae isolates from children with invasive pneumococcal disease in Turkey: baseline evaluation of the introduction of the pneumococcal conjugate vaccine nationwide.

Systemic lupus erythematosus due to Epstein-Barr virus or Epstein-Barr virus infection provocating acute exacerbation of systemic lupus erythematosus?

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Tuberculin skin test response in patients with juvenile idiopathic arthritis on anti-TNF therapy