Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Fehime Kara Eroglu"'
Autor:
Ulku Guler, Muzaffer Yildirim, Volkan Yazar, Deniz Karakaya, Tugce Yildirim, Eda Çiftci Dede, Fehime Kara Eroglu, Ihsan Gursel, Tülin Güngör, Evra Çelikkaya, Nilsu Turay, Mehmet Bülbül, Petek Korkusuz, Bekir Salih
Publikováno v:
American Journal of Physiology: Renal Physiology
Since previous research suggests a role of a circulating factor in the pathogenesis of steroid-sensitive nephrotic syndrome (NS), we speculated that circulating plasma extracellular vesicles (EVs) are a candidate source of such a soluble mediator. He
Autor:
Elif Çomak, Gul Ozcelik, Midhat Elmaci, Nuran Kucuk, Ismail Dursun, Mithat Büyükçelik, Funda Bastug, Pelin Ertan, Ali Delibaş, Bahriye Atmis, Bağdagül Aksu, Beltinge Demircioglu Kilic, Tülin Güngör, Demet Alaygut, Fehime Kara Eroglu, Yılmaz Tabel, Berfin Uysal, Ipek Ozunan, Sebahat Tulpar, Nurdan Yildiz, Nilüfer Göknar, Serra Sürmeli Döven, Mehtap Akbalik Kara, Ayse Balat, Ferah Sönmez, Cemile Pehlivanoglu, Gamze Seval Ozzorlar, Ayşe Ağbaş, Atilla Gemici, Engin Melek
Publikováno v:
Pediatric Nephrology. 37:393-402
© 2021, IPNA.Background: Children are one of the most vulnerable groups in conflict zones, especially those with chronic diseases. This study aimed to investigate kidney disease profiles and problems during follow-up in a population of Syrian refuge
Autor:
Michael Ludwig, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Gökçe Gür, Fehime Kara Eroglu, Mehmet Bülbül, Tülin Güngör
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Dent disease is a rare X-linked recessive tubular disorder, characterized by the triad of low molecular-weight proteinuria, hypercalciuria, nephrocalcinosis and/or nephrolithiasis. It is caused by mutations in the CLCN5 gene or OCRL gene. Thirty to 8
Autor:
Fehime Kara Eroglu, Sami Ulus Maternity Rheumatology, Fatma Yazılıtaş, Çiğdem Üner, Mehmet Bülbül, Nilüfer Arda, Deniz Karakaya, Eda Didem Kurt Şükür, Evrim Kargın Çakıcı, Gökçe Can, Tülin Güngör, Evra Çelikkaya
Publikováno v:
Turkish Journal of Nephrology. 28:250-256
Autor:
Fehime Kara Eroglu, Gökçe Can, Evrim Kargın Çakıcı, Mehmet Bülbül, Tülin Güngör, Evra Çelikkaya, Fatma Yazılıtaş
Publikováno v:
Ortadoğu Tıp Dergisi. 11:193-199
Aim: Chronic kidney disease is associated with some hematologic changes such as decreased platelet production, platelet dysfunction and thrombocytosis. The inflammatory markers increase in chronic kidney disease. Mean platelet volume, the ratio of ne
Autor:
Mehmet Bülbül, Eda Didem Kurt Şükür, Gökçe Gür, Fehime Kara Eroglu, Esra Bağlan, Fatma Yazılıtaş, Semanur Özdel, Tülin Güngör, Evra Çelikkaya, Sare Gülfem Özlü, Evrim Kargın Çakıcı
Publikováno v:
Clinical Rheumatology. 38:1947-1952
To explore the frequency of MEFV gene mutations in children with Henoch-Schönlein purpura who had no prior familial Mediterranean fever diagnosis and to evaluate the association of MEFV mutations with the clinical and laboratory features of Henoch-S
Autor:
Rezan Topaloglu, Z. Birsin Özçakar, Fatih Ozaltin, Fehime Kara Eroglu, Ali Duzova, Safak Gucer, Fatma Tuba Eminoğlu, Diclehan Orhan, Nazli Gonc, Rahsan Gocmen, Ayfer Alikasifoglu, Dilek Yalnizoglu, Hulya Nalcacioglu
Publikováno v:
Pediatric Neurology. 88:71-74
Ozcakar, Zeynep/0000-0002-6376-9189; DUZOVA, ALI/0000-0002-4365-2995; Gocmen, Rahsan/0000-0002-0223-9336 WOS: 000455971500011 PubMed: 30337132 BACKGROUND: COQ2 mutations cause a rare infantile multisystemic disease with heterogeneous clinical feature
Autor:
Cengiz Candan, Bora Gülhan, Ayşe Ağbaş, Seha Saygili, Fehime Kara Eroglu, Mutlu Hayran, Harika Alpay, Zeynep Birsin Özçakar, Emine Atayar, Alper Soylu, Selçuk Yüksel, Oguz Soylemezoglu, Fatih Ozaltin, Gulsah Ozdemir, Ali Duzova, Belde Kasap Demir, Rezan Topaloglu
Background: Alport syndrome (AS) is an inherited glomerular disease caused by mutations in COL4A3, COL4A4, or COL4A5. Associations between clinical manifestations and genotype are not yet well defined. Our study aimed to define clinical and genetic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be8e9d496555e6775770c95fdec9f0e
https://avesis.deu.edu.tr/publication/details/a3ecaa5d-449d-4203-95ea-ea9e03007e05/oai
https://avesis.deu.edu.tr/publication/details/a3ecaa5d-449d-4203-95ea-ea9e03007e05/oai
Autor:
Mehmet Bülbül, Evrim Kargın Çakıcı, Eda Didem Kurt-Şükür, Deniz Karakaya, Tülin Güngör, Evra Çelikkaya, Fatma Yazılıtaş, Semanur Özdel, Fehime Kara Eroglu, Esra Bağlan
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 63(6)
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 this study was to describe the presenting features, etiology, and clinical characteristics of
Autor:
Alper Soylu, Mutlu Hayran, Harika Alpay, Emine Atayar, Bora Gülhan, Oguz Soylemezoglu, Cengiz Candan, Fehime Kara Eroglu, Ayşe Ağbaş, Rezan Topaloglu, Nur Canpolat, Belde Kasap Demir, Z. Birsin Özçakar, Fatih Ozaltin, Selçuk Yüksel, Gulsah Ozdemir, Ali Duzova
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Alport syndrome (AS) is an inherited glomerular basement membrane disease caused by mutations in COL4A3, COL4A4 or COL4A5 genes. Recently, it has been reported that focal segmental glomerulosclerosis (FSGS) can be seen in AS and C