Lista de obras - Ayca Kiykim - Dominio Público Uruguay

Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis

artículo científico publicado en 2017

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

artículo científico publicado en 2017

Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

artículo científico publicado en 2017

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

artículo científico publicado en 2018

Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation.

artículo científico publicado en 2017

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

artículo científico publicado en 2015

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

artículo científico publicado en 2018

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

scientific article published on 19 July 2019

Immune system defects in DiGeorge syndrome and association with clinical course

scientific article published on 09 September 2019

JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family

artículo científico publicado en 2015

LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency

artículo científico publicado en 2020

Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study.

artículo científico publicado en 2017

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

scientific article published on 17 November 2019

Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study

artículo científico publicado en 2015

Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimicking ATM mutated patients

artículo científico publicado en 2020

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

artículo científico publicado en 2015

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

artículo científico publicado en 2016

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

artículo científico publicado en 2017

The evaluation of malignancies in Turkish primary immunotherapy patients; a multicenter study

artículo científico publicado en 2020

Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.

artículo científico publicado en 2013

Lista de obras de Ayca Kiykim

Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation.

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

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

Immune system defects in DiGeorge syndrome and association with clinical course

JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family

LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency

Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study.

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study

Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimicking ATM mutated patients

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

The evaluation of malignancies in Turkish primary immunotherapy patients; a multicenter study

Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.