Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Funda Erol Cipe"'
Publikováno v:
Journal of Clinical Immunology. 40:539-542
BOZKURT, CEYHUN/0000-0001-6771-9894; FIRTINA, Sinem/0000-0002-3370-8545; Erman, Baran/0000-0001-9398-8465 Erman, Baran ; Firtina, Sinem ; Bozkurt, Ceyhun ; Cipe, Funda Erol (isu author) T cell receptor (TCR) complex consists of αβ or γδ TCR chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a3c25a37dff88385af0308d7e304f6
https://doi.org/10.1007/s10875-020-00752-3
https://doi.org/10.1007/s10875-020-00752-3
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:
Dilara Fatma Kocacık Uygun, Vedat Uygun, Yuk Yin Ng, Ismail Reisli, Safa Baris, Serdar Nepesov, Esra Hazar Sayar, Yildiz Camcioglu, Funda Erol Cipe, Tuba Cogurlu, Elif Karakoç Aydıner, Selda Hançerli Törün, Ozden Hatirnaz Ng, Ahmet Ozen, Muge Sayitoglu, Ugur Ozbek, Ayca Kiykim, Aysenur Kaya, Şükrü Çekiç, Deniz Cagdas, Isil Eser Simsek, Sinem Firtina, Esra Yücel
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
https://doi.org/10.1111/iji.12496
Autor:
Baran Erman, Funda Erol Cipe
Publikováno v:
Pediatr Allergy Immunol Pulmonol
Erman, Baran/0000-0001-9398-8465 Background: Primary immunodeficiencies (PIDs) are a heterogeneous group of congenital disorders characterized by susceptibility to recurrent infections, allergy, malignancies and autoimmunity. The identification of di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc4d8bdfe38bf7463623c9647a031794
https://doi.org/10.1089/ped.2019.1097
https://doi.org/10.1089/ped.2019.1097
Autor:
Funda Erol Cipe, Ali Onder Atca, Ceyhun Bozkurt, Murat Sütçü, Ayhan Yaman, Özlem Başoğlu Öner, Tunç Fışgın, Başak Adaklı Aksoy
Publikováno v:
Turk Arch Pediatr
Coronavirus disease 2019 (COVID-19) is a pandemic that spread rapidly worldwide (1). So far, very few reports concerning the impact of COVID-19 among patients with pediatric hematologic-oncologic diseases are available (2). We aimed to describe the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eba9c90b9f6952eedfa7738b9436065
https://pubmed.ncbi.nlm.nih.gov/34104923
https://pubmed.ncbi.nlm.nih.gov/34104923
Autor:
Gurcan Dikme, Ceyhun Bozkurt, Başak Adaklı Aksoy, Esra Yücel, Funda Erol Cipe, Selime Aydogdu, Cigdem Aydogmus, Tunç Fışgın, Ayca Kiykim
Publikováno v:
Pediatric transplantationREFERENCES. 25(7)
Background Primary immunodeficiency diseases (PID) are characterized by the occurrence of frequent infections and are caused by many genetic defects. Hematopoietic stem cell transplantation (HSCT) is the only curative treatment option for the majorit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e3473ee6b4cf9dcf71681befab04e9b
https://pubmed.ncbi.nlm.nih.gov/34092004
https://pubmed.ncbi.nlm.nih.gov/34092004
Autor:
Baran Erman, Gonca Erkose Genc, Başak Adaklı Aksoy, Öner Doğan, Funda Erol Cipe, Selime Aydogdu, Sinem Firtina, Ceyhun Bozkurt, Tunç Fışgın
BOZKURT, CEYHUN/0000-0001-6771-9894; FIRTINA, Sinem/0000-0002-3370-8545; Erman, Baran/0000-0001-9398-8465 Erman, Baran ; Firtina, Sinem ; Adakli Aksoy, Basak ; Bozkurt, Ceyhun ; Cipe, Funda Erol (isu author) Purpose Autosomal recessive (AR) CARD9 def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555fb49020ad8da81341942c22f8dbee
https://hdl.handle.net/20.500.12713/450
https://hdl.handle.net/20.500.12713/450
Publikováno v:
European Oral Research. 81:145-148
DOI : 10.26650/IUITFD.348181 Amac : Cocuk sagligi izlemi temel ilkeleri arasinda cocuklarda buyume ve gelismeyi degerlendirmek, riskli durumlari belirlemek, riskli durumlarda cozum plani olusturmak yer almaktadir. Calismamizin amaci, cocuk sagligi iz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6afbb4238bb6eb85f91851d6c997ba73
https://doi.org/10.26650/iuitfd.348181
https://doi.org/10.26650/iuitfd.348181
Autor:
Ayse Deniz Yucelten, Sevgi Bilgic Eltan, Funda Erol Cipe, Velat Celik, Burcu Kocamis, Mehmet Halil Çeliksoy, Ercan Nain, Elif Karakoc-Aydiner, Safa Baris, Ahmet Ozen, Dilek Baser, Emre Akkelle, Sakine Isik, Ayca Kiykim, Nurhan Kasap, Ismail Ogulur, Pakize Cennetoglu
Hyper-IgE syndrome (HIES) patients may share many features observed in severe atopic dermatitis (SAD), making a diagnostic dilemma for physicians. Determining clinical and laboratory markers that distinguish both disorders could provide early diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5e32a9e37f6376bc4b4896580f7fcab
https://aperta.ulakbim.gov.tr/record/233152
https://aperta.ulakbim.gov.tr/record/233152
Autor:
Ana Krolo, Ayca Kiykim, Serap Karaman, Zeynep Tamay, Esra Yücel, Raul Jimenez Heredia, Safa Baris, Kaan Boztug, Ahmet Ozen, Funda Erol Cipe, Ibrahim Serhat Karakus, Elif Karakoc-Aydiner
Purpose: Recently, a new form of congenital neutropenia that is caused by germline biallelic loss-of-function mutations in the SMARCD2 gene was described in four patients. Given the rarity of the condition, the clinical spectrum of the disease has re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ac5f462fde39b697987ba844dbd789
https://hdl.handle.net/20.500.12713/1139
https://hdl.handle.net/20.500.12713/1139