Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Şükrü Nail Güner"'
Autor:
Mehmet Kocaoğlu, Burcu Ezgi Kocaoğlu, Selma Erol Aytekin, Doğukan Mustafa Keskin, Şükrü Nail Güner, Sevgi Keleş, İsmail Reisli
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 1, Pp 38-45 (2023)
Background: IgG subclass deficiency is a laboratory diagnosis and becomes important with recurrent infections. This study aimed to examine the demographic, clinical, and laboratory results of pediatric cases with IgG subclass deficiency and to improv
Externí odkaz:
https://doaj.org/article/0e829ff5e77846c4a5239ae678d6eb9d
Autor:
Alişan Yıldıran, Mehmet Halil Çeliksoy, Stephan Borte, Şükrü Nail Güner, Murat Elli, Tunç Fışgın, Emel Özyürek, Recep Sancak, Gönül Oğur
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 345-349 (2017)
Hematopoietic stem cell transplantation is a promising curative therapy for many combined primary immunodeficiencies and phagocytic disorders. We retrospectively reviewed pediatric cases of patients diagnosed with primary immunodeficiencies and sched
Externí odkaz:
https://doaj.org/article/40a7f80699034bb0b31d693305518a8b
Autor:
Hasan Kapakli, Havva Bozkurt Alan, Şükrü Nail Güner, Esra Hazar, Ismail Reisli, Yahya Gul, Sevgi Keles
Publikováno v:
Journal of Clinical Immunology. 42:64-71
The aim was to review the compliance, side effects and effectiveness of subcutaneous immunoglobulin (SCIG) supplementation in patients with primary immunodeficiencies (PID) who had previously received intravenous immunoglobulin (IVIG) therapy and sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c279b9baefb82acffdb6396a32d9238
https://doi.org/10.1007/s10875-021-01144-x
https://doi.org/10.1007/s10875-021-01144-x
Autor:
Mehmet Kocaoğlu, Burcu Ezgi Kocaoğlu, Selma Erol Aytekin, Doğukan Mustafa Keskin, Şükrü Nail Güner, Sevgi Keleş, İsmail Reisli
Publikováno v:
Pediatrics and neonatology.
Makale
WOS:000922080700001
PubMed ID: 36089538
Background: IgG subclass deficiency is a laboratory diagnosis and becomes important with recurrent infections. This study aimed to examine the demographic, clinical, and laboratory results
WOS:000922080700001
PubMed ID: 36089538
Background: IgG subclass deficiency is a laboratory diagnosis and becomes important with recurrent infections. This study aimed to examine the demographic, clinical, and laboratory results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b8011baf8d4832c543dee493770b422
https://pubmed.ncbi.nlm.nih.gov/36089538
https://pubmed.ncbi.nlm.nih.gov/36089538
Autor:
Özlem Bayram, Ismail Reisli, Sevgi Köstel Bal, Gunseli Bozdogan, Kaan Boztug, Klara Dalva, Aydan Ikinciogullari, Tanıl Kendirli, Caner Aytekin, Mutlu Yuksek, Nazmiye Kurşun, Candan Islamoglu, Şükrü Nail Güner, Sule Haskologlu, Alisan Yildiran, Deniz Bayrakoğlu, Figen Dogu, Funda Erol Cipe
Publikováno v:
Journal of Clinical Immunology. 41:1563-1573
Severe combined immunodeficiency is an inborn error of immunity characterized by impairments in the numbers and functions of T and B lymphocytes due to various genetic causes, and if it remains untreated, patients succumb to infections during the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f70175dfb114703a6c4fbf2c586ff7e
https://doi.org/10.1007/s10875-021-01062-y
https://doi.org/10.1007/s10875-021-01062-y
Autor:
Sule Haskologlu, Senem Kocak, Lale Satiroglu Tufan, Fethiye Eken Aksoy, Dilan Bastug, Deniz Aslar Oner, Candan Islamoglu, Kubra Baskin, Saliha Esenboga, Deniz Acican, Serdar Ceylaner, Sukru Nail Guner, Sevgi Keles, Deniz Cagdas, Ismail Reisli, Basak Tezel, Figen Dogu, Ilhan Tezcan, Aydan Ikinciogullari
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
PurposeThe measurement of T-cell receptor excision circle (TREC) is used for newborn screening (NBS) in dried blood spot (DBS) samples from Guthrie card for severe combined immunodeficiency (SCID). Here, we report the results of first newborn screeni
Externí odkaz:
https://doaj.org/article/63d40995e82a4174924d76686bdbaf14
Autor:
Fadime Ceyda Eldeniz, Yahya Gül, Alaattin Yorulmaz, Şükrü Nail Güner, Sevgi Keles, İsmail Reisli
Objective: Ten warning signs of primary immunodeficiency (PID) were suggested by the Jeffrey Modell Foundation (JMF), to increase physician awareness of PID. These warning signs have not yet been evaluated for patients with secondary immunodeficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e682c0df9f5725c8b6d0dc3fa248df8
https://doi.org/10.21203/rs.3.rs-1189503/v1
https://doi.org/10.21203/rs.3.rs-1189503/v1
Autor:
Seyma Celikbilek Celik, Şükrü Nail Güner, Ercan Kurar, Mehmet Ali Karaselek, Sevgi Keles, Ismail Reisli, Hasan Kapakli
Publikováno v:
Pediatric Allergy and Immunology. 30:668-671
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e38f7024955a9295a0a312d9b12146a
https://doi.org/10.1111/pai.13056
https://doi.org/10.1111/pai.13056
Autor:
Melanie Wong, Danielle T. Avery, Ismail Reisli, Matÿfffedas M. Oleastro, David Zahra, Winnie Ip, Stuart G. Tangye, Cindy S. Ma, Imogen Moran, Siobhan O. Burns, Robert Brink, Kathryn Payne, Elissa K. Deenick, E. Graham Davies, Şükrü Nail Güner, Christopher C. Goodnow, Sevgi Keles, Tri Giang Phan, Luigi D. Notarangelo, Helen Lenthall
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:2302-2305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::879ab4843caa435f42448e4efb71aee0
https://doi.org/10.1016/j.jaci.2019.02.010
https://doi.org/10.1016/j.jaci.2019.02.010
Publikováno v:
Selcuk Tip Dergisi. 1:63-68
\n 1p36 Deletion Syndrome is a rare disease characterized by a partial deletion in the short arm of chromosome 1. The first reports of cases with microdeletion of chromosome 1p36 were published in 1980s, beginning with a report by Hain et al. The fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03e93b521dcfbe53aaf822ab94b295d6
https://doi.org/10.30733/std.2019.01065
https://doi.org/10.30733/std.2019.01065