Search Results - "Eke Gungor, Hatice"

Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity by Meric, Zeynep, Gemici Karaaslan, Betul, Yalcin Gungoren, Ezgi, Bektas Hortoglu, Melika, Cavas, Tolga, Aydemir, Sezin, Bilgic Eltan, Sevgi, Firtina, Sinem, Kendir Demirkol, Yasemin, Eser, Metin, Cekic, Sukru, Kilic, Suar, Karasu, Gulsun, Yesilipek, Mehmet Akif, Eke Gungor, Hatice, Karakoc‐Aydiner, Elif, Ozen, Ahmet, Baris, Safa, Yucel, Esra, Cokugras, Haluk, Kiykim, Ayca

“…Background Artemis deficiency is an autosomal recessive disorder characterized by a combined immunodeficiency with increased cellular radiosensitivity. In this…”
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Increased plasma soluble human leukocyte antigen‐G in persistent wheezy infants by Tahan, Fulya, Eke Gungor, Hatice, Akar, Himmet Haluk, Saraymen, Berkay

“…Background Human leukocyte antigen (HLA)‐G is a non‐classical major histocompatibility complex class I antigen characterized by limited polymorphism in its…”
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DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome by Oktelik, Fatma Betul, Wang, Muyun, Keles, Sevgi, Eke Gungor, Hatice, Cansever, Murat, Can, Salim, Karakoc-Aydiner, Elif, Baris, Safa, Schmitz-Abe, Klaus, Benamar, Mehdi, Chatila, Talal A.

“…Dedicator of cytokinesis 8 (DOCK8) deficiency underlies the majority of cases of patients with autosomal recessive form of the hyper-immunoglobulin E syndrome…”
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Pollen allergy and eosinophilic esophagitis by Eke Güngör, Hatice, Arslan, Duran, Deniz, Kemal, Tahan, Fulya

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Myeloperoxidase deficiency: the secret under the flag of unstained cell by Patıroğlu, Türkan, Eke Güngör, Hatice, Belohradsky, Julie Sawalle, Unal, Ekrem, Klein, Christoph

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Laboratory, Clinical and Genetic Characteristics of Cases with Chronic Granulomatous Diseases: the Erciyes University Experience by Gungor, Hatice Eke, Patiroglu, Turkan, Unal, Ekrem

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Decreased levels of lipoxin A4 and annexin A1 in wheezy infants by Eke Gungor, Hatice, Tahan, Fulya, Gokahmetoglu, Selma, Saraymen, Berkay

“…Wheezing is a common and challenging health issue in infancy and early childhood. Asthma diagnosis is frequent in patients with a history of recurrent…”
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A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia by Goktas, Serdar, Azizoglu, Zehra B., Petersheim, Daniel, Erdogan, Merve, Eke Gungor, Hatice, Bisgin, Atil, Tuğ Bozdoğan, Sevcan, Eken, Ahmet, Unal, Ekrem, Klein, Christoph, Patiroglu, Turkan

“…Severe congenital neutropenia (SCN) is a rare disease. Autosomal recessive forms of SCN are more frequent in countries where consanguineous marriages are…”
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Is yoga training beneficial for exercise-induced bronchoconstriction? by Tahan, Fulya, Eke Gungor, Hatice, Bicici, Emine

“…Some studies have shown the beneficial effects of yoga for individuals with bronchial hyperreactivity with regard to (1) a reduction in the use of rescue…”
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The efficacy of Pelargonium sidoides in the treatment of upper respiratory tract infections in children with transient hypogammaglobulinemia of infancy by Patiroglu, Turkan, Tunc, Aydin, Eke Gungor, Hatice, Unal, Ekrem

“…Transient hypogammaglobulinemia of infancy (THI), defined as prolongation of physiological hypogammaglobulinemia normally seen between the initial 3rd and 6th…”
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Gastric signet ring carcinoma in a patient with ataxia-telangiectasia: a case report and review of the literature by Patiroglu, Turkan, Eke Gungor, Hatice, Arslan, Duran, Deniz, Kemal, Unal, Ekrem, Coskun, Abdulhakim

“…Ataxia-telangiectasia (A-T) is an autosomal recessive primary immunodeficiency disease characterized by progressive cerebellar ataxia, telangiectasia,…”
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Effect of montelukast on clinical score and cytokine levels of infants for clinically diagnosed acute bronchiolitis by Tahan, Fulya, Celik, Serkan, Eke Gungor, Hatice

“…Acute bronchiolitis comprises a major cause for morbidity in infants with viral infection which induces an immune inflammatory response that may produce long…”
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The plasma gelsolin levels in atopic dermatitis: Effect of atopy and disease severity by Eke Gungor, Hatice, Sahiner, Umit Murat, Karakukcu, Cigdem, Sahiner, Neriman, Altuner Torun, Yasemin

“…Gelsolin is an actin-binding protein with several cellular functions including anti-apoptosis and is reported to have an anti-inflammatory effect. Apoptosis of…”
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Minipuberty period of children with atopic dermatitis compared to healthy children by KOCA, Serkan Bilge, GÜNGÖR, Hatice Eke, CANSEVER, Murat

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Myeloperoxidase deficiency: the secret under the flag of unstained cell / Myeloperoksidaz Eksikligi, Boyanmamis Hucre Bayragi Altindaki Gizem by Pattroglu, Tiirkan, Gungor, Hatice Eke, Belohradsky, Julie Sawalle, Unal, Ekrem, K1ein, Christoph

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Serum sRAGE levels in children with atopic dermatitis: a prospective study by Eke-Gungor, Hatice, Sagiroglu, Bilal, Can-Coskun, Zehra Nur, Kocer, Derya, Karakukcu, Çiğdem

“…Atopic dermatitis (AD) is chronic inflammatory skin disorder. The receptor for advanced glycation end products (RAGE) plays a role in inflammatory reactions…”
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Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency by Le Voyer, Tom, Sakata, Sonoko, Tsumura, Miyuki, Khan, Taushif, Esteve-Sole, Ana, Al-Saud, Bandar K, Gungor, Hatice Eke, Taur, Prasad, Jeanne-Julien, Valentine, Christiansen, Mette, Köhler, Lisa-Maria, ElGhazali, Gehad Eltayeb, Rosain, Jérémie, Nishimura, Shiho, Sakura, Fumiaki, Bouaziz, Matthieu, Oleaga-Quintas, Carmen, Nieto-Patlán, Alejandro, Deyà-Martinez, Àngela, Altuner Torun, Yasemin, Neehus, Anna-Lena, Roynard, Manon, Bozdemir, Sefika Elmas, Al Kaabi, Nawal, Al Hassani, Moza, Mersiyanova, Irina, Rozenberg, Flore, Speckmann, Carsten, Hainmann, Ina, Hauck, Fabian, Alzahrani, Mohammed Hamdan, Alhajjar, Sami Hussain, Al-Muhsen, Saleh, Cole, Theresa, Fuleihan, Ramsay, Arkwright, Peter D, Badolato, Raffaele, Alsina, Laia, Abel, Laurent, Desai, Mukesh, Al-Mousa, Hamoud, Shcherbina, Anna, Marr, Nico, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Okada, Satoshi, Bustamante, Jacinta

“…Autosomal recessive (AR) STAT1 deficiency is a severe inborn error of immunity disrupting cellular responses to type I, II, and III IFNs, and IL-27, and…”
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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients by Yakici, Nalan, Kreins, Alexandra Y., Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Gungor, Hatice Eke, Cea, Pablo A., Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Altunbas, Melek Yorgun, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D., Davies, E. Graham, Baris, Safa

“…Paired box 1 (PAX1) deficiency has been reported in a small number of patients diagnosed with otofaciocervical syndrome type 2 (OFCS2). We described six new…”
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Factors that predict disease severity in atopic dermatitis: The role of serum basal tryptase by Sahiner, Umit Murat, Buyuktiryaki, Betul, Gungor, Hatice Eke, Sahiner, Neriman, Turasan, Abdullah, Torun, Yasemin Altuner, Sekerel, Bulent Enis

“…Increased numbers of mast cells that contain tryptase are found in lesional atopic dermatitis (AD) skin. The association of serum basal tryptase (sBT) with…”
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A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia by Goktas, Serdar, Azizoglu, Zehra B., Petersheim, Daniel, Erdogan, Merve, Eke Gungor, Hatice, Bisgin, Atil, Tuğ Bozdoğan, Sevcan, Eken, Ahmet, Unal, Ekrem, Klein, Christoph, Patiroglu, Turkan

“…Severe congenital neutropenia (SCN) is a rare disease. Autosomal recessive forms of SCN are more frequent in countries where consanguineous marriages are…”
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