Search Results - "Bora, Gulhan"

Extra-Renal manifestations of atypical hemolytic uremic syndrome in children by Fidan, Kibriya, Göknar, Nilüfer, Gülhan, Bora, Melek, Engin, Yıldırım, Zeynep Y., Baskın, Esra, Hayran, Mutlu, Gülleroglu, Kaan, Özçakar, Zeynep B., Ozaltin, Fatih, Soylemezoglu, Oguz

“…Background Atypical hemolytic uremic syndrome (aHUS) is a chronic disease characterized by thrombotic microangiopathy and a high risk of end-stage kidney…”
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Variable phenotype and genotype of pediatric patients with HNF1B nephropathy by Gülhan, Bora, Ekici, Ozan, Dursun, İsmail, Göknar, Nilüfer, Yüksel, Selçuk, Alaygut, Demet, Özçakar, Zeynep Birsin, Nalçacıoğlu, Hülya, Demircioğlu Kılıç, Beltinge, Söylemezoğlu, Oğuz, Duzova, Ali, Topaloglu, Rezan, Ozaltin, Fatih

“…Hepatocyte nuclear factor 1β ( ) mutations are the most common monogenic cause of congenital anomalies of the kidney and urinary tract (CAKUT). We aimed to…”
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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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Calcineurin inhibitor‐related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature by Unsal, Yagmur, Baltu, Demet, Gulhan, Bora, Okur, Fatma Visal, Ozaltın, Fatih, Düzova, Ali, Topaloğlu, Rezan, Ozon, Zeynep Alev, Gonç, Elmas Nazlı

“…Introduction Calcineurin inhibitors (CNIs) are widely used in transplantation. Although CNI‐related hyperkalemia is common (10%–60.6%), the underlying…”
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Cystinosis beyond kidneys: gastrointestinal system and muscle involvement by Topaloglu, Rezan, Gültekingil, Ayşe, Gülhan, Bora, Ozaltin, Fatih, Demir, Hülya, Çiftci, Türkmen, Demir, Numan, Temucin, Çağrı Mesut, Yuce, Aysel, Akhan, Okhan

“…Cystinosis is a multisystemic disease resulting from cystine accumulation primarily in kidney and many other tissues. We intended to study the evolution of…”
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Transplantation in pediatric aHUS within the era of eculizumab therapy by Özçakar, Zeynep Birsin, Ozaltin, Fatih, Gülhan, Bora, Çomak, Elif, Parmaksız, Gönül, Baskın, Esra, Topaloğlu, Rezan, Kasap Demir, Belde, Canpolat, Nur, Yuruk Yildirim, Zeynep, Demircioğlu Kılıç, Beltinge, Yüksel, Selçuk, Söylemezoğlu, Oğuz

“…aHUS is caused by the over‐activation and dysregulation of the alternative complement pathway. Data regarding outcomes of pediatric aHUS patients after kidney…”
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Short Bowel Syndrome Is Not a Contraindication for Kidney Transplantation by Tastemel Ozturk, Tugba, Gulhan, Bora, Gumus, Ersin, Hizarcioglu‐Gulsen, Hayriye, Kurt‐Sukur, Eda Didem, Bozaci, Ali Cansu, Aki, Fazil Tuncay, Duzova, Ali, Topaloglu, Rezan, Ozaltin, Fatih

“…ABSTRACT Background Short bowel syndrome (SBS) is a malabsorptive condition that develops as a result of massive resection of the small intestine and causes…”
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Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis by Nemutlu, Emirhan, Ozaltin, Fatih, Yabanoglu-Ciftci, Samiye, Gulhan, Bora, Eylem, Cemil Can, Baysal, İpek, Gök-Topak, Elif Damla, Ulubayram, Kezban, Sezerman, Osman Ugur, Ucar, Gulberk, Kır, Sedef, Topaloglu, Rezan

“…Cystinosis is a rare, devastating hereditary disease secondary to recessive gene mutations. The most commonly used diagnostic method is confirmation of an…”
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PAI-1 and tPA gene polymorphisms and susceptibility to chronic obstructive pulmonary disease in a sample of Turkish population by Aysel Sunnetcioglu, Mehmet Berkoz, Metin Yildirim, Gulhan Bora, Serap Yalin

“…Abstract Objective: The aim of this study was to assess the influence of plasminogen activator inhibitor-1 (PAI-1) 4G/5G or tissue plasminogen activator (tPA)…”
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Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases by Tastemel Ozturk, Tugba, Kanbur, Nuray, Ozmert, Elif Nursel, Gulhan, Bora, Ozaltin, Fatih, Topaloglu, Rezan, Duzova, Ali

“…Complementary and alternative medicine are treatments administered alone or in combination with conventional medical treatments. Data on complementary and…”
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Acute kidney injury in a patient with COVID-19: Answers by Tastemel Ozturk, Tugba, Baltu, Demet, Kurt Sukur, Eda Didem, Ozsurekci, Yasemin, Gucer, Safak, Basaran, Ozge, Gulhan, Bora, Ozaltin, Fatih, Duzova, Ali, Topaloglu, Rezan

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Acute kidney injury in a patient with COVID-19: Questions by Tastemel Ozturk, Tugba, Baltu, Demet, Kurt Sukur, Eda Didem, Ozsurekci, Yasemin, Gucer, Safak, Basaran, Ozge, Gulhan, Bora, Ozaltin, Fatih, Duzova, Ali, Topaloglu, Rezan

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Case Report: Severe McCune-Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles by Unsal, Yagmur, Gozmen, Onur, User, İdil Rana, Hızarcıoglu, Hayriye, Gulhan, Bora, Ekinci, Saniye, Karagoz, Tevfik, Ozon, Z Alev, Gonc, E Nazlı

“…Café-au-lait skin macules, Cushing syndrome (CS), hyperthyroidism, and liver and cardiac dysfunction are presenting features of neonatal McCune-Albright…”
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Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients by Besbas, Nesrin, Gulhan, Bora, Soylemezoglu, Oguz, Ozcakar, Z Birsin, Korkmaz, Emine, Hayran, Mutlu, Ozaltin, Fatih

“…Atypical hemolytic uremic syndrome (aHUS) is a devastating disease with significant morbidity and mortality. Its genetic heterogeneity impacts its clinical…”
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Different features of lung involvement in Niemann-Pick disease and Gaucher disease by Gülhan, Bora, Özçelik, Uğur, Gürakan, Figen, Güçer, Şafak, Orhan, Diclehan, Cinel, Güzin, Yalçn, Ebru, Ersöz, Deniz Doğru, Kiper, Nural, Yüce, Aysel, Kale, Gülsev

“…Summary Background Niemann-Pick disease (NPD) and Gaucher disease (GD) are well-known lysosomal storage diseases. Respiratory system involvement is an…”
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Bisphosphonates in juvenile dermatomyositis with dystrophic calcinosis by Tayfur, Asli Celebi, Topaloglu, Rezan, Gulhan, Bora, Bilginer, Yelda

“…Abstract Objectives. Our primary objective was to retrospectively analyze whether bisphosphonates initiated in combination with immunosuppressive drugs and/or…”
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Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients: a cross-sectional web-based survey by Wente-Schulz, Sarah, Aksenova, Marina, Awan, Atif, Ambarsari, Cahyani Gita, Becherucci, Francesca, Emma, Francesco, Fila, Marc, Francisco, Telma, Gokce, Ibrahim, Gülhan, Bora, Hansen, Matthias, Jahnukainen, Timo, Kallash, Mahmoud, Kamperis, Konstantinos, Mason, Sherene, Mastrangelo, Antonio, Mencarelli, Francesca, Niwinska-Faryna, Bogna, Riordan, Michael, Rus, Rina R, Saygili, Seha, Serdaroglu, Erkin, Taner, Sevgin, Topaloglu, Rezan, Vidal, Enrico, Woroniecki, Robert, Yel, Sibel, Zieg, Jakub, Pape, Lars

“…BackgroundAcute tubulointerstitial nephritis (TIN) is a significant cause of acute renal failure in paediatric and adult patients. There are no large…”
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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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Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome? by Özlü, Sare Gülfem, Gülhan, Bora, Aydoğ, Özlem, Atayar, Emine, Delibaş, Ali, Parmaksız, Gönül, Özdoğan, Elif Bahat, Çomak, Elif, Taşdemir, Mehmet, Acar, Banu, Özçakar, Zeynep Birsin, Topaloğlu, Rezan, Söylemezoğlu, Oğuz, Özaltın, Fatih

“…Atypical hemolytic uremic syndrome (aHUS) occurs due to defective regulation of the alternative complement pathway (ACP) on vascular endothelial cells. Plasma…”
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Meningococcal Carriage in Children with Atypical Hemolytic Uremic Syndrome Receiving Eculizumab Therapy by Kavaz Tufan, Asli, Ozak Batibay, Fatma, Kaya Aksoy, Gulsah, Gulhan, Bora, Demircioglu Kilic, Beltinge, Dursun, Ismail, Buyukkaragoz, Bahar, Caltik Yilmaz, Aysun, Nalcacioglu, Hulya, Becerir, Tulay, Cetin, Nuran, Celegen, Kubra, Dinleyici, Meltem, Kaya, Mucahit, Kilic, Omer, Dinleyici, Ener Cagri

“…Eculizumab is a first-line treatment for atypical hemolytic uremic syndrome (aHUS), and patients undergoing eculizumab therapy may become more susceptible to…”
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