Search Results - "Eroglu, Fehime Kara"

CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood by Eroglu, Fehime Kara, Orhan, Diclehan, İnözü, Mihriban, Duzova, Ali, Gulhan, Bora, Ozaltin, Fatih, Topaloglu, Rezan

“…Background CD80 (also known as B7‐1) is a co‐stimulatory molecule that is expressed in biopsies and also excreted in urine in patients with minimal change…”
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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey by Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

“…Alström syndrome (ALMS) is an autosomal recessive disease characterized by multiple organ involvement, including neurosensory vision and hearing loss,…”
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Value of renal pelvic diameter and urinary tract dilation classification in the prediction of urinary tract anomaly by Cakici, Evrim Kargin, Aydog, Ozlem, Eroglu, Fehime Kara, Yazilitas, Fatma, Ozlu, Sare Gulfem, Uner, Cigdem, Renda, Rahime, Yılmaz, Engin, Bulbul, Mehmet

“…Background The aim of this study was to identify the cut‐offs of postnatal anteroposterior renal pelvic diameter (APRPD), according to the urinary tract…”
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Retrospective analysis of simple and stage II renal cysts: Pediatric nephrology point of view by Eroglu, Fehime Kara, Kargın Çakıcı, Evrim, Can, Gökçe, Güngör, Tülin, Yazılıtaş, Fatma, Kurt‐Sukur, Eda Didem, Celikkaya, Evra, Üner, Çiğdem, Çakmakçı, Emin, Bülbül, Mehmet

“…Background Increased ultrasonography (US) use has been correlated with an increased incidence of pediatric renal cysts. For simple and stage II cysts, the…”
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Indications and Outcomes of Renal Biopsies in Children: A Single-Center 12-Year Experience by Kargin Cakici, Evrim, Yazilitas, Fatma, Uner, Cigdem, Can, Gokce, Kurt Sukur, Eda Didem, Gungor, Tulin, Celikkaya, Evra, Kara Eroglu, Fehime, Karakaya, Deniz, Arda, Nilufer, Bulbul, Mehmet

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Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency by Gul, Ersin, Sayar, Esra Hazar, Gungor, Bilgi, Eroglu, Fehime Kara, Surucu, Naz, Keles, Sevgi, Guner, Sukru Nail, Findik, Siddika, Alpdundar, Esin, Ayanoglu, Ihsan Cihan, Kayaoglu, Basak, Geckin, Busra Nur, Sanli, Hatice Asena, Kahraman, Tamer, Yakicier, Cengiz, Muftuoglu, Meltem, Oguz, Berna, Cagdas Ayvaz, Deniz Nazire, Gursel, Ihsan, Ozen, Seza, Reisli, Ismail, Gursel, Mayda

“…Pathological inflammatory syndromes of unknown etiology are commonly observed in ataxia telangiectasia (AT) and Artemis deficiency. Similar inflammatory…”
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Failure to thrive, interstitial lung disease, and progressive digital necrosis with onset in infancy by Chia, Justin, MD, Eroglu, Fehime Kara, MD, MS, Özen, Seza, MD, Orhan, Dicle, MD, Montealegre-Sanchez, Gina, MD, MS, de Jesus, Adriana A., MD, PhD, Goldbach-Mansky, Raphaela, MD, MHSc, Cowen, Edward W., MD, MHSc

“…Key teaching points • SAVI is a recently described interferonopathy resulting from constitutive action of STING and up-regulation of IFN-β signaling. • SAVI is…”
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A retrospective analysis of children with Henoch–Schonlein purpura and re-evaluation of renal pathologies using Oxford classification by Çakıcı, Evrim Kargın, Gür, Gökçe, Yazılıtaş, Fatma, Eroğlu, Fehime Kara, Güngör, Tülin, Arda, Nilüfer, Orhan, Diclehan, Özalp Ateş, Funda Seher, Bülbül, Mehmet

“…Background Henoch–Schönlein purpura (HSP) is the most common vasculitis in childhood. The long-term prognosis is variable and depends on renal involvement. The…”
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Plasma Extracellular Vesicles Derived from Pediatric COVID-19 Patients Modulate Monocyte and T Cell Immune Responses Based on Disease Severity by Cetinkaya, Pınar Gur, Abras, Irem Fatma, Evcili, Irem, Yildirim, Tugçe, Ceylan, Yasemin, Kara Eroglu, Fehime, Kayaoglu, Başak, İpekoglu, Emre Mert, Akarsu, Aysegul, Yıldırım, Muzaffer, Kahraman, Tamer, Cengiz, Ali Bülent, Sahiner, Umit Murat, Sekerel, Bulent Enis, Ozsurekci, Yasemin, Soyer, Ozge, Gursel, Ihsan

“…The COVID-19 pandemic has caused significant morbidity and mortality globally. The role of plasma-derived extracellular vesicles (EVs) in pediatric COVID-19…”
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An Extremely Rare Cause of Prolonged Menstruation: Lupus Anticoagulant-Hypoprothrombinemia Syndrome by Ozdel, Semanur, Baglan, Esra, Azapağası, Ebru Ünal, Eroglu, Fehime Kara, Kargın Cakıcı, Evrim, Bulbul, Mehmet

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Clinical characteristics of childhood acute tubulointerstitial nephritis by Güngör, Tülin, Çakıcı, Evrim Kargın, Yazılıtaş, Fatma, Eroğlu, Fehime Kara, Özdel, Semanur, Kurt‐Sukur, Eda Didem, Çelikkaya, Evra, Karakaya, Deniz, Bağlan, Esra, Bülbül, Mehmet

“…Background Acute tubulointerstitial nephritis (ATIN) is a rare cause of acute kidney injury in children that can lead to chronic kidney disease. The aim of…”
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Anxiety and depression in children with primary monosymptomatic nocturnal enuresis and their mothers by Yazilitaş, Fatma, Açikel, Burak, Çakici, Evrim Kargin, Güngör, Tülin, Çelikkaya, Evra, Eroğlu, Fehime Kara, Karakaya, Deniz, Can, Gökçe, Kurt Şükür, Eda Didem, Bülbül, Mehmet

“…The aim of this prospective study is to investigate the presence of anxiety and depression in children with PMNE and their mothers. This is a cross-sectional…”
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Canakinumab treatment in children with familial Mediterranean fever: report from a single center by Yazılıtaş, Fatma, Aydoğ, Özlem, Özlü, Sare Gülfem, Çakıcı, Evrim Kargın, Güngör, Tülin, Eroğlu, Fehime Kara, Gür, Gökçe, Bülbül, Mehmet

“…Familial Mediterranean fever (FMF), the most common hereditary autoinflammatory disorder is characterized by recurrent episodes of fever, serositis, arthritis…”
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Evaluation of the level of dynamic thiol/disulphide homeostasis in adolescent patients with newly diagnosed primary hypertension by Çakıcı, Evrim Kargın, Eroğlu, Fehime Kara, Yazılıtaş, Fatma, Bülbül, Mehmet, Gür, Gökçe, Aydoğ, Özlem, Güngör, Tülin, Erel, Özcan, Alışık, Murat, Elhan, Atilla Halil

“…Background Thiol/disulphide homeostasis plays a critical role in numerous intracellular enzymatic pathways including antioxidant defense and detoxification…”
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Publisher Correction: Evaluation of the level of dynamic thiol/disulphide homeostasis in adolescent patients with newly diagnosed primary hypertension by Çakıcı, Evrim Kargın, Eroğlu, Fehime Kara, Yazılıtaş, Fatma, Bülbül, Mehmet, Gür, Gökçe, Aydoğ, Özlem, Güngör, Tülin, Erel, Özcan, Alışık, Murat, Elhan, Atilla Halil

“…Owing to an error in typesetting, the name of the author Atilla Halil Elhan was rendered wrongly. The original publication has now been corrected in this…”
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The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome by Özdemir, Gülşah, Kara Eroğlu, Fehime, Kasap Demir, Belde, Yüksel, Selçuk, Tabel, Yılmaz, Ağbaş, Ayşe, Düzova, Ali, Hayran, Mutlu, Özaltın, Fatih, Bayazıt, Aysun Karabay, Yılmaz, Alev, Söylemezoğlu, Oğuz, Gülhan, Bora, Kurt-Şükür, Eda Didem, Atayar, Emine, Atan, Raziye, Dursun, İsmail, Özçakar, Zeynep Birsin, Saygılı, Seha, Soylu, Alper, Topaloğlu, Rezan

“…Background. Alport syndrome (AS) is characterized by progressive kidney disease. There is increasing evidence that renin-angiotensin-aldosterone system (RAAS)…”
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A case of Type 1 Dent disease presenting with isolated persistent proteinuria by Güngör, Tülin, Eroğlu, Fehime Kara, Yazılıtaş, Fatma, Gür, Gökçe, Çakıcı, Evrim Kargın, Ludwig, Michael, Bülbül, Mehmet

“…Dent disease is a rare X-linked recessive tubular disorder, characterized by the triad of low molecular-weight proteinuria, hypercalciuria, nephrocalcinosis…”
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Mucolipidosis Type III: A Rare Disease in Differential Diagnosis of Joint Stiffness in Pediatric Rheumatology by Kasapkara, Çiğdem Seher, Akçaboy, Meltem, Kara Eroğlu, Fehime, Derinkuyu, Betül Emine

“…Mucolipidoses are metabolic disorders with autosomal recessive inheritance caused by deficiency of N-acetylglucosamine- 1-phosphotransferase leading to…”
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Periodic Fever, Aphthosis, Pharyngitis, and Adenitis Syndrome: Analysis of Patients From Two Geographic Areas by Batu, Ezgi D., Kara Eroğlu, Fehime, Tsoukas, Paul, Hausmann, Jonathan S., Bilginer, Yelda, Kenna, Margaret A., Licameli, Greg R., Fuhlbrigge, Robert C., Özen, Seza, Dedeoğlu, Fatma

“…Objective Periodic fever, aphthosis, pharyngitis, and adenitis (PFAPA) syndrome is a periodic fever syndrome of childhood with an unknown etiology. Our aim was…”
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Sarcoidosis del adulto de inicio en la infancia: a proposito de un caso by Ozsurekci, Yasemin, Cengiz, Ali B., Duzova, Ali, Sag, Erdal, Kadayifcilar, Sibel, Dogru Ersoz, Deniz, Akcoren, Zuhal, Yuce, Aysel, Tavil, Betul, Ayvaz, Deniz, Akyuz, Canan, Kara Eroglu, Fehime

“…La sarcoidosis, un trastorno multiorgánico de etiología desconocida que afecta varios órganos, es poco frecuente en los niños. Se desconocen la incidencia y la…”
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