Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sevgi Kostel Bal"'
Autor:
Marini Thian, Birgit Hoeger, Anton Kamnev, Fiona Poyer, Sevgi Köstel Bal, Michael Caldera, Raúl Jiménez-Heredia, Jakob Huemer, Winfried F. Pickl, Miriam Groß, Stephan Ehl, Carrie L. Lucas, Jörg Menche, Caroline Hutter, Andishe Attarbaschi, Loïc Dupré, Kaan Boztug
Publikováno v:
Haematologica, Vol 105, Iss 10 (2020)
Externí odkaz:
https://doaj.org/article/05a1e3b218284012a40d802819712505
Autor:
Tala Shahin, Dominik Aschenbrenner, Deniz Cagdas, Sevgi Köstel Bal, Cecilia Domínguez Conde, Wojciech Garncarz, David Medgyesi, Tobias Schwerd, Betül Karaatmaca, Pınar Gur Cetinkaya, Saliha Esenboga, Stephen R. F. Twigg, Andrew Cant, Andrew O. M. Wilkie, Ilhan Tezcan, Holm H. Uhlig, Kaan Boztug
Publikováno v:
Haematologica, Vol 104, Iss 3 (2019)
Hyper-IgE syndromes comprise a group of inborn errors of immunity. STAT3-deficient hyper-IgE syndrome is characterized by elevated serum IgE levels, recurrent infections and eczema, and characteristic skeletal anomalies. A loss-of-function biallelic
Externí odkaz:
https://doaj.org/article/993b7a64cd5a4ba09b8c642f3bc48b4d
Autor:
Şule Haskoloğlu, Ayşenur Öztürk, Gökcan Öztürk, Sevgi Kostel Bal, Candan İslamoğlu, Kübra Baskın, Serdar Ceylaner, Lale Tufan Satıroğlu, Figen Doğu, Aydan İkincioğulları
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 271-281 (2020)
Objective: Wiskott-Aldrich syndrome (WAS) is an X-linked primary immune deficiency characterized by microthrombocytopenia, eczema, and recurrent infections. We aimed to evaluate the clinical features and outcomes of a WAS cohort. Materials and Method
Externí odkaz:
https://doaj.org/article/b2a4303dd604422d8c7f3c088b9c2ad8
Autor:
Ayse Yesbek Kaymaz, Sevgi Kostel Bal, Gamze Bora, Beril Talim, Alev Ozon, Ayfer Alikasifoglu, Haluk Topaloglu, Hayat Erdem Yurter
Publikováno v:
Muscle & Nerve. 66:631-638
Spinal muscular atrophy (SMA) is an inherited neuromuscular disease caused by survival motor neuron (SMN) protein deficiency. Insulin-like growth factor-I (IGF-I) is a myotrophic and neurotrophic factor that has been reported to be dysregulated in in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7636b3cc1ae6679f6914ad7f039cadf
https://doi.org/10.1002/mus.27715
https://doi.org/10.1002/mus.27715
Autor:
Ozlem, Bayram, Sule, Haskologlu, Deniz, Bayrakoğlu, Sevgi Kostel, Bal, Candan, Islamoglu, Funda Erol, Cipe, Tanil, Kendirli, Nazmiye, Kursun, Sukru Nail, Guner, Alisan, Yildiran, Gunseli, Bozdogan, Mutlu, Yuksek, Ismail, Reisli, Klara, Dalva, Caner, Aytekin, Kaan, Boztug, Figen, Dogu, Aydan, Ikinciogullari
Publikováno v:
Journal of clinical immunology. 41(7)
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=pmid________::a6092061c3933a5da717753e48aeaa06
https://pubmed.ncbi.nlm.nih.gov/34114123
https://pubmed.ncbi.nlm.nih.gov/34114123
Autor:
Bilgehan Yalçın, Hilal Susam-Sen, Ayse Sevgi Kostel Bal, Ali Varan, Canan Akyüz, Tezer Kutluk, Burca Aydin
Publikováno v:
ResearcherID
Wilms tumor is the most common renal malignancy of childhood. Because of the improvement in prognosis and the increase in survival rates, long-term consequences of the treatment for Wilms tumor are of greater concern. We investigated late renal effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2572873564aee471b98ca49e9a10a522
https://doi.org/10.1097/mph.0000000000000557
https://doi.org/10.1097/mph.0000000000000557
