Lista de obras - Güzide Aksu - Dominio Público Uruguay

A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients

artículo científico publicado en 2015

A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome

artículo científico publicado en 2009

A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity

artículo científico publicado en 2014

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

artículo científico publicado en 2011

Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections

artículo científico publicado en 2007

Association between anti-endomysial antibody and total intestinal villous atrophy in children with coeliac disease

artículo científico publicado en 2003

Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey

artículo científico publicado en 2011

Autoantibodies Other than Antineutrophil Cytoplasmic Antibodies Are Not Positive in Patients with Psoriasis Vulgaris

BCG-osis and tuberculosis in a child with chronic granulomatous disease

scholarly article by Jacinta Bustamante et al published July 2007 in The Journal of Allergy and Clinical Immunology

CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency

artículo científico publicado en 2015

Chronic inflammatory bowel disease in a patient with common variable immunodeficiency.

artículo científico publicado en 2001

Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.

artículo científico publicado en 2009

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

artículo científico publicado en 2004

Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings.

artículo científico publicado en 2010

Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study

artículo científico publicado en 2010

Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin. Immunol. 110 (2004) 22–29]

scholarly article published in Clinical Immunology

Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency

artículo científico publicado en 2006

Decreased ratio of CD4/CD8 lymphocytes might be predictive for successful interferon alpha and lamivudine combined therapy in childhood chronic hepatitis B infection: A preliminary study

artículo científico publicado en 2003

Determination of cut-off titers and agreement between immunofluorescence and immunoblotting methods for detecting antinuclear antibodies in children

artículo científico publicado en 2010

Determination of intracellular Th1/Th2 type cytokines in lymphocytes of chronic hepatitis B patients treated with interferon-alpha

artículo científico publicado en 2010

Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.

artículo científico publicado en 2009

Do elevated serum IgM levels have to be included in probable diagnosis criteria of patients with ataxia-telangiectasia?

artículo científico publicado en 2014

Does OM-85 BV prophylaxis trigger autoimmunity in IgA deficient children?

artículo científico publicado en 2011

Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

scientific article published on 17 September 2013

Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

artículo científico publicado en 2016

Effect of immunotherapy on autoimmune parameters in children with atopic asthma

artículo científico publicado en 2002

Evaluation of the immunomodulatory properties in mice and in vitro anti-inflammatory activity of cycloartane type saponins from Astragalus species

artículo científico publicado en 2011

Evaluation of transforming growth factor-beta 1 level in crevicular fluid of cyclosporin A-treated patients

artículo científico publicado en 2001

Fc gamma RIIa, IIIa and IIIb polymorphisms in Turkish children susceptible to recurrent infectious diseases.

artículo científico publicado en 2006

Fc receptor-like proteins (FCRL): immunomodulators of B cell function

artículo científico publicado en 2007

Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections

artículo científico publicado en 2015

First report of successful stem cell transplantation in a child with CD40 deficiency

artículo científico publicado en 2007

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

artículo científico publicado en 2010

Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency.

artículo científico publicado en 2012

Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: Expanding the phenotypic spectrum ofRab27Amutations in humans

scientific article published on 01 February 2003

Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.

artículo científico publicado en 2008

Hyper-immunoglobulin M syndrome type 3 with normal CD40 cell surface expression

artículo científico publicado en 2012

Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever

artículo científico publicado en 2006

Idiopathic CD4+ T cell lymphocytopenia with the absence of B cells and CD8+28+ cells in peripheral blood.

artículo científico publicado en 2002

IgG-anti-IgA antibodies: an autoimmune finding in patients with psoriasis vulgaris.

artículo científico publicado en 2012

Immune Deficiencies following Cancer Treatment in Children

artículo científico publicado en 2003

Immune status and autoantibody formation in children with chronic hepatitis B infection

artículo científico publicado en 2002

Immunoglobulin light chain levels can be used to determine disease stage in children with juvenile idiopathic arthritis

artículo científico publicado el 1 de enero de 2011

Increased percentages of autoantibodies in immunoglobulin A-deficient children do not correlate with clinical manifestations

artículo científico publicado en 2009

Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency

artículo científico publicado en 2007

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

artículo científico publicado en 2015

Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report

artículo científico publicado en 2015

Inverse relationship between the ratio of ICAM-1 expressing lymphocytes and serum TGF-beta 1 concentrations in acute rheumatic fever

artículo científico publicado en 2005

Is There an Association between Autoimmune Hemolytic Anemia and Ataxia-Telangiectasia?

scientific article published on 01 September 2000

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

artículo científico publicado en 2006

Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications

artículo científico publicado en 2003

MYCOBACTERIUM FORTUITUM-CHELONAE COMPLEX INFECTION IN A CHILD WITH COMPLETE INTERLEUKIN-12 RECEPTOR BETA 1 DEFICIENCY

artículo científico publicado en 2001

Mannose-binding lectin may affect pregnancy outcome

artículo científico publicado en 2015

Maternally acquired varicella-zoster virus antibodies disappear at 6 months of age in prematurely born children

artículo científico publicado en 2003

New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy

artículo científico publicado en 2010

Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

artículo científico publicado en 2012

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

artículo científico publicado en 2013

Permanent neonatal diabetes with arthrogryposis multiplex congenita and neurogenic bladder - a new syndrome?

artículo científico publicado en 2006

Pesticide-induced scleroderma and early intensive immunosuppressive treatment

artículo científico publicado en 2012

Prepubertal periodontitis associated with chronic granulomatous disease

artículo científico publicado en 2001

Progressive morphea of early childhood tracing Blaschko’s lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis

artículo científico publicado en 2011

Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections

artículo científico publicado en 2007

Quinacrine-induced psychiatric disturbances in a child with common variable immunodeficiency and chronic giardiasis.

artículo científico publicado en 2002

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

artículo científico publicado en 2016

Relapsing polychondritis in a child with common variable immunodeficiency

artículo científico publicado en 2009

Renal involvement as a rare complication of Dorfman-Chanarin syndrome: a case report

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Serum immunoglobulin (IgG, IgM, IgA) and IgG subclass concentrations in healthy children: a study using nephelometric technique

artículo científico publicado en 2006

Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature

artículo científico publicado en 2011

Successful bone marrow transplantation in an 8-month-old patient with chronic granulomatous disease

scientific article published on 01 July 2006

The effect of clotting factor concentrates on the immune system in HIV-negative haemophilics

artículo científico publicado en 2005

The influence of marginal zinc deficient diet on post-vaccination immune response against hepatitis B in rats

artículo científico publicado en 2006

The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study

artículo científico publicado en 2012

Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency

artículo científico publicado en 2012

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis

artículo científico publicado en 2011

Lista de obras de Güzide Aksu

A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients

A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome

A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections

Association between anti-endomysial antibody and total intestinal villous atrophy in children with coeliac disease

Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey

Autoantibodies Other than Antineutrophil Cytoplasmic Antibodies Are Not Positive in Patients with Psoriasis Vulgaris

BCG-osis and tuberculosis in a child with chronic granulomatous disease

CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency

Chronic inflammatory bowel disease in a patient with common variable immunodeficiency.

Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings.

Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study

Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin. Immunol. 110 (2004) 22–29]

Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency

Decreased ratio of CD4/CD8 lymphocytes might be predictive for successful interferon alpha and lamivudine combined therapy in childhood chronic hepatitis B infection: A preliminary study

Determination of cut-off titers and agreement between immunofluorescence and immunoblotting methods for detecting antinuclear antibodies in children

Determination of intracellular Th1/Th2 type cytokines in lymphocytes of chronic hepatitis B patients treated with interferon-alpha

Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.

Do elevated serum IgM levels have to be included in probable diagnosis criteria of patients with ataxia-telangiectasia?

Does OM-85 BV prophylaxis trigger autoimmunity in IgA deficient children?

Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

Effect of immunotherapy on autoimmune parameters in children with atopic asthma

Evaluation of the immunomodulatory properties in mice and in vitro anti-inflammatory activity of cycloartane type saponins from Astragalus species

Evaluation of transforming growth factor-beta 1 level in crevicular fluid of cyclosporin A-treated patients

Fc gamma RIIa, IIIa and IIIb polymorphisms in Turkish children susceptible to recurrent infectious diseases.

Fc receptor-like proteins (FCRL): immunomodulators of B cell function

Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections

First report of successful stem cell transplantation in a child with CD40 deficiency

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency.

Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: Expanding the phenotypic spectrum ofRab27Amutations in humans

Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.

Hyper-immunoglobulin M syndrome type 3 with normal CD40 cell surface expression

Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever

Idiopathic CD4+ T cell lymphocytopenia with the absence of B cells and CD8+28+ cells in peripheral blood.

IgG-anti-IgA antibodies: an autoimmune finding in patients with psoriasis vulgaris.

Immune Deficiencies following Cancer Treatment in Children

Immune status and autoantibody formation in children with chronic hepatitis B infection

Immunoglobulin light chain levels can be used to determine disease stage in children with juvenile idiopathic arthritis

Increased percentages of autoantibodies in immunoglobulin A-deficient children do not correlate with clinical manifestations

Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report

Inverse relationship between the ratio of ICAM-1 expressing lymphocytes and serum TGF-beta 1 concentrations in acute rheumatic fever

Is There an Association between Autoimmune Hemolytic Anemia and Ataxia-Telangiectasia?

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications

MYCOBACTERIUM FORTUITUM-CHELONAE COMPLEX INFECTION IN A CHILD WITH COMPLETE INTERLEUKIN-12 RECEPTOR BETA 1 DEFICIENCY

Mannose-binding lectin may affect pregnancy outcome

Maternally acquired varicella-zoster virus antibodies disappear at 6 months of age in prematurely born children

New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy

Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

Permanent neonatal diabetes with arthrogryposis multiplex congenita and neurogenic bladder - a new syndrome?

Pesticide-induced scleroderma and early intensive immunosuppressive treatment

Prepubertal periodontitis associated with chronic granulomatous disease

Progressive morphea of early childhood tracing Blaschko’s lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis

Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections

Quinacrine-induced psychiatric disturbances in a child with common variable immunodeficiency and chronic giardiasis.

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

Relapsing polychondritis in a child with common variable immunodeficiency

Renal involvement as a rare complication of Dorfman-Chanarin syndrome: a case report

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

Serum immunoglobulin (IgG, IgM, IgA) and IgG subclass concentrations in healthy children: a study using nephelometric technique

Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature

Successful bone marrow transplantation in an 8-month-old patient with chronic granulomatous disease

The effect of clotting factor concentrates on the immune system in HIV-negative haemophilics

The influence of marginal zinc deficient diet on post-vaccination immune response against hepatitis B in rats

The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study

Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis