Výsledky vyhledávání - "Serdar, Nepesov"

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

Autor: Ömer Faruk Beşer, Ayca Kiykim, Ali Islek, Serdar Nepesov, Gokhan Baysoy, Elif Karakoc-Aydiner, Sezin Aydemir, Yöntem Yaman, Haluk Cokugras, Bernice Lo, Yasemin Kendir Demirkol, Safa Baris, Satanay Hubrack, Fügen Çullu Çokuğraş, Ahmet Ozen

Publikováno v: Journal of Clinical Immunology. 41:1406-1410

To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, nutrient- and growth fact

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567d8f10960dce77ea7682b64e613444
https://doi.org/10.1007/s10875-021-01042-2

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MİKOBAKTERİYEL HASTALIKLARA MENDEL DUYARLILIĞI HASTALARININ GENETİK VE KLİNİK PROFİLİ; TEK MERKEZ DENEYİMİ

Autor: Serdar Nepesov, Sinem Fırtına, Fatma Aygün, Begüm Işıkgil, Yıldız Çamcıoğlu, Ayça Kıykım, Esra Özek Yücel, Yasemin Kendir Demirkol, Akif Ayaz

Publikováno v: Journal of Advanced Research in Health Sciences
Sağlık Bilimlerinde İleri Araştırmalar Dergisi

Objective: Mendelian susceptibility to mycobacterial disease (MSMD) is a subgroup of primary immunodeficiencies which develops with the Bacille Calmette–Guérin (BCG) vaccine or non-tuberculous mycobacterial infections. The clinical symptoms have a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::227aac91289e3d8bc20bfd4a0e005915
https://dergipark.org.tr/tr/pub/sabiad/issue/71413/1119899

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Decreased frequency of allergy in juvenile idiopathic arthritis: Results of a case-control study

Autor: Ozgur Kasapcopur, Sezgin Sahin, Haluk Cokugras, Kenan Barut, Pinar Ozge Avar-Aydin, Serdar Nepesov, Amra Adrovic

Publikováno v: Modern Rheumatology. 31:697-703

To determine the frequency of Th2-mediated allergic diseases (AD) in mainly Th1-driven juvenile idiopathic arthritis (JIA) subtypes.Ninety-nine JIA patients and 128 control subjects were enrolled in a prospective case-control study. All subjects were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22197df252b91dd15674cef55cb7576
https://doi.org/10.1080/14397595.2020.1812820

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Mutational landscape of severe combined immunodeficiency patients from Turkey

Publikováno v: International Journal of Immunogenetics. 47:529-538

Severe combined immunodeficiency (SCID) has a diverse genetic aetiology, where a clinical phenotype, caused by single and/or multiple gene variants, can give rise to multiple presentations. The advent of next-generation sequencing (NGS) has recently

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67f61fd3e6f44116032505b85653c0e9
https://doi.org/10.1111/iji.12496

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Diagnosis of primary immunodeficiency diseases in pediatric patients hospitalized for recurrent, severe, or unusual infections

Autor: Serdar Nepesov, Sinem Firtina, Fatma Deniz Aygun, Nihan Burtenece, Haluk Cokugras, Yildiz Camcioglu

Publikováno v: Allergologia et immunopathologia. 50(4)

Background: Primary immunodeficiency diseases (PID) usually presents itself with recurrent, severe, and unusual infections, along with autoimmunity and various other malignancies. But, the diversity of PID often makes the diagnosis of patients diffic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80cb2d9bb3b7792cb16e1ec274c57e6c
https://pubmed.ncbi.nlm.nih.gov/35789402

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