Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Elif Azarsız"'
Autor:
Sanem Eren Akarcan, Ezgi Ulusoy Severcan, Neslihan Edeer Karaca, Esra Isik, Guzide Aksu, Mélanie Migaud, Ferda Evin Gurkan, Elif Azarsiz, Anne Puel, Jean-Laurent Casanova, Necil Kutukculer
Publikováno v:
Case Reports in Immunology, Vol 2017 (2017)
Chronic Mucocutaneous Candidiasis (CMC) is the chronic, recurrent, noninvasive Candida infections of the skin, mucous membranes, and nails. A 26-month-old girl was admitted with the complaints of recurrent oral Candidiasis, diarrhea, and respiratory
Externí odkaz:
https://doaj.org/article/42bfc2653cc34033abf21a0a43d26970
Publikováno v:
Pediatric Reports, Vol 5, Iss 3, Pp e14-e14 (2013)
Transient hypogammaglobulinemia of infancy (THI) is characterized by recurrent infections and one or more reduced serum immunoglobulin levels. Typically, THI patients recover spontaneously, mostly within 30-40 months of age, but sometimes recovery ma
Externí odkaz:
https://doaj.org/article/39e75e3797b84943acb7f7869137ee81
Autor:
Hale Tuhan, Aslı Aslan, Çiğdem Ecevit, Elif Azarsız, Neslihan Karaca, Funda Çetin, Necil Kütükçüler, Güzide Aksu
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 3, Pp 172-178 (2020)
Aim:We aimed to determine the frequency of autoantibody antinuclear (ANA), peripheral anti-neutrophil cytoplasmic antibody (p-ANCA), anti-Saccharomyces cerevisiae antibody (ASCA), anti-pancreatic exocrine gland antibody (PAb), goblet cell antibody (G
Externí odkaz:
https://doaj.org/article/1b12a8dc4192440a8b8cef32d0578eec
Autor:
Zümrüt Şahbudak Bal, Nihal Karadaş Özdemir, Semra Şen, Deniz Yılmaz Karapınar, Elif Azarsız, Şöhret Aydemir, Fadıl Vardar
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 3, Pp 254-257 (2017)
Despite improvements in diagnosis and treatment, infections are still a major cause of morbidity and mortality in children with febrile neutropenia. In the majority of febrile episodes, the source of infection cannot be defined. In this study, we aim
Externí odkaz:
https://doaj.org/article/ad1bec95489c4ba5b9ad4263e47d441c
Autor:
Belkız, Öngen, Sema, Kalkan Uçar, Ertürk, Levent, Elif, Azarsız, Turan, Koloğlu, Mahmut, Çoker, Eser, Sözmen, Ferhan G, Sağın
Publikováno v:
Annals of clinical biochemistry. 54(5)
Background Inflammation and hypercholesterolaemia contribute to atherosclerotic changes which can start in childhood. Children with hyperlipidaemias are at high risk for early coronary atherosclerosis. This study evaluates the relationship between li
Autor:
Neslihan Karaca Edeer, Güzide Aksu, Nesrin Gülez, Elif Azarsız, Kaan Kavaklı, Christoph Klein, Necil Kütükçüler
Amaç: Ağır konjenital nötropeniler, nadir görülen matür nötrofillerin eksikliği ile karakterize immün yetersizlik hastalığıdır. Çalışmamızda amaç Ege Üniversitesi Tıp Fakültesi Pediatrik İmmünoloji Kliniğimizde izlenen ve gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9436::f3406d9159b764c368b34465e56d4dff
https://hdl.handle.net/11454/9060
https://hdl.handle.net/11454/9060
İnterlökin (IL)-12/interferon (IFN)-? yolaklarında yer alan genlerdeki mutasyonlar ve nükleer faktör kappa-B temel modülatörü (Nuclear factor-kB Essential Modulator; NEMO) mutasyonları gibi konjenital hücresel immün yetmezliği olan bebekl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9436::2975d56566b98ed45075a8710b0c65ee
https://hdl.handle.net/11454/9262
https://hdl.handle.net/11454/9262
Autor:
Mehmet Yalaz, Sema Tanriverdi, Özgün Uygur, Özge Altun Köroğlu, Elif Azarsiz, Guzide Aksu, Nilgün Kültürsay
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundRespiratory distress syndrome (RDS) is the most common respiratory disease in premature infants. Exogenous natural surfactant preparations are used in the treatment of RDS. In recent years, it has become increasingly evident that surfactant
Externí odkaz:
https://doaj.org/article/44a0eb8c42554d5bbbb148d4549eba18
Autor:
Nesrin Gulez, Guzide Aksu, Afig Berdeli, Neslihan Karaca, Sema Tanrıverdi, Necil Kutukculer, Elif Azarsiz
Publikováno v:
Case Reports in Medicine, Vol 2011 (2011)
The X-linked lymphoproliferative syndrome (XLP) is a rare, inherited immunodeficiency characterized by recurrent episodes of hemophagocytic lymphohistiocytosis, hypogammaglobulinemia, and/or lymphomas. Recently, X-linked inhibitor of apoptosis (XIAP/
Externí odkaz:
https://doaj.org/article/202664f712e64df09417153076386f1a
Autor:
Neslihan Edeer Karaca, Guzide Aksu, Nesrin Gulez, Basak Yildiz, Elif Azarsiz, Necil Kutukculer
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Iss No. 4 (2010)
Transient hypogammaglobulinemia (THI) of infancy is a common primary immunodeficiency usually resolves by 3 years of age. In this study, clinical, immunological data and outcome of 101 retrospectively diagnosed THI patients were evaluated. Majority o
Externí odkaz:
https://doaj.org/article/ef0c5e7c1ed14ba2896621db601d6ee4