Search research articles
Contact Us
Filters
Showing results (21-30 of 52) with videos related to
Page
of 6
Sort By:
Parasitology International
|
April 21, 2006
A novel mutation for TAP deficiency and its possible association with Toxoplasmosis
Figen Doğu, Aydan Ikincioğullari, Dominique Fricker, et al.
Pediatric Transplantation
|
January 23, 2008
An unconditioned bone marrow transplantation in a child with purine nucleoside phosphorylase deficiency and its unique complication
Caner Aytekin, Mutlu Yuksek, Figen Dogu, et al.
Frontiers in Immunology
|
May 8, 2026
Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency
Sule Haskologlu, Caner Aytekin, Candan Islamoglu, et al.
Journal of Cellular and Molecular Medicine
|
June 12, 2024
Whole-exome sequencing for genetic diagnosis of idiopathic liver injury in children
Aysima Atılgan Lülecioğlu, Yılmaz Yücehan Yazıcı, Alperen Baran, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
February 29, 2020
Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency
Sule Haskologlu, Sevgi Kostel Bal, Candan Islamoglu, et al.
Pediatric Transplantation
|
May 19, 2012
HLA-haploidentical transplantations for primary immunodeficiencies: a single-center experience
Funda Erol Cipe, Figen Dogu, Caner Aytekin, et al.
Human Molecular Genetics
|
July 29, 2016
Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals
Haoyu Wu, Peter E Thijssen, Eleonora de Klerk, et al.
Frontiers in Immunology
|
October 23, 2025
Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations
Sule Haskologlu, Aydan Ikinciogullari, Candan Islamoglu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 15, 2025
DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report
Deniz Yasar, Abdullah Sezer, Caner Aytekin, et al.
Clinical Genetics
|
May 20, 2021
Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis-plus syndrome in two siblings
Yılmaz Yıldız, Can Koşukcu, Damla Aygün, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Parasitology International
|
April 21, 2006
A novel mutation for TAP deficiency and its possible association with Toxoplasmosis
Figen Doğu, Aydan Ikincioğullari, Dominique Fricker, et al.
Pediatric Transplantation
|
January 23, 2008
An unconditioned bone marrow transplantation in a child with purine nucleoside phosphorylase deficiency and its unique complication
Caner Aytekin, Mutlu Yuksek, Figen Dogu, et al.
Frontiers in Immunology
|
May 8, 2026
Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency
Sule Haskologlu, Caner Aytekin, Candan Islamoglu, et al.
Journal of Cellular and Molecular Medicine
|
June 12, 2024
Whole-exome sequencing for genetic diagnosis of idiopathic liver injury in children
Aysima Atılgan Lülecioğlu, Yılmaz Yücehan Yazıcı, Alperen Baran, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
February 29, 2020
Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency
Sule Haskologlu, Sevgi Kostel Bal, Candan Islamoglu, et al.
Pediatric Transplantation
|
May 19, 2012
HLA-haploidentical transplantations for primary immunodeficiencies: a single-center experience
Funda Erol Cipe, Figen Dogu, Caner Aytekin, et al.
Human Molecular Genetics
|
July 29, 2016
Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals
Haoyu Wu, Peter E Thijssen, Eleonora de Klerk, et al.
Frontiers in Immunology
|
October 23, 2025
Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations
Sule Haskologlu, Aydan Ikinciogullari, Candan Islamoglu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 15, 2025
DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report
Deniz Yasar, Abdullah Sezer, Caner Aytekin, et al.
Clinical Genetics
|
May 20, 2021
Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis-plus syndrome in two siblings
Yılmaz Yıldız, Can Koşukcu, Damla Aygün, et al.
Page
of 6