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Comprehensive analysis of pediatric urolithiasis in a tertiary care center and insights into demographics, risk factors, and management outcomes 三级护理中心儿科尿石症的全面分析以及对人口统计学、危险因素和管理结果的见解 Kavgaci, Umay; Gulhan, Bora; Kurt-Sukur, Eda Didem; Duzova, Ali; Dogan, Hasan Serkan; Tekgul, Serdar; Topaloglu, Rezan; Ozaltin, Fatih 分享 收藏
The clinical characteristics of patients with congenital nephrotic syndrome secondary to NPHS1 mutation: Is nephrectomy still a therapeutic option for selected cases? (may, 10.1007/s00467-025-06774-6, 2025) 先天性肾病综合征患者（继发于NPHS1突变）的临床特征：对于特定病例，肾切除术是否仍是一种治疗选择？(2025年5月，10.1007/s00467-025-06774-6) Ugurlu, Yueksel; Gulhan, Bora; Dursun, Ismail; Nalcacioglu, Hulya; Kaya Aksoy, Guelsah; Canpolat, Nur; Bayazit, Aysun; Ozcakar, Zeynep Birsin; Yuksel, Selcuk; Parmaksiz, Goenuel; Ozdemir, Gulsah; Kurt-Sukur, Eda Didem; Duzova, Ali; Hayran, Mutlu; Ozaltin, Fatih 分享 收藏
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence Kachmar, Jessica; Boyer, Olivia; Lipska-Zietkiewicz, Beata; Moriniere, Vincent; Gribouval, Olivier; Heidet, Laurence; Balasz-Chmielewska, Irena; Benetti, Elisa; Cloarec, Sylvie; Csaicsich, Dagmar; Decramer, Stephane; Gellermann, Jutta; Guigonis, Vincent; Hogan, Julien; Bayazit, Aysun Karabay; Melk, Anette; Nigmatullina, Nazym; Oh, Jun; Ozaltin, Fatih; Ranchin, Bruno; Tsimaratos, Michel; Trautmann, Agnes; Antignac, Corinne; Schaefer, Franz; Dorval, Guillaume 分享 收藏
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) Riedhammer, Korbinian M.; Nguyen, Thanh-Minh T.; Kosukcu, Can; Calzada-Wack, Julia; Li, Yong; Batzir, Nurit Assia; Saygili, Seha; Wimmers, Vera; Kim, Gwang-Jin; Chrysanthou, Marialena; Bakey, Zeineb; Sofrin-Drucker, Efrat; Kraiger, Markus; Sanz-Moreno, Adrian; Amarie, Oana V.; Rathkolb, Birgit; Klein-Rodewald, Tanja; Garrett, Lillian; Hoelter, Sabine M.; Seisenberger, Claudia; Haug, Stefan; Schlosser, Pascal; Marschall, Susan; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Wuttke, Matthias; de Angelis, Martin Hrabe; Comic, Jasmina; Dogan, Ozlem Akgun; Ozluk, Yasemin; Tasdemir, Mehmet; Agbas, Ayse; Canpolat, Nur; Orenstein, Naama; Caliskan, Salim; Weber, Ruthild G.; Bergmann, Carsten; Jeanpierre, Cecile; Saunier, Sophie; Lim, Tze Y.; Hildebrandt, Friedhelm; Alhaddad, Bader; Basel-Salmon, Lina; Borovitz, Yael; Wu, Kaman; Antony, Dinu; Matschkal, Julia; Schaaf, Christian W.; Renders, Lutz; Schmaderer, Christoph; Rogg, Manuel; Schell, Christoph; Meitinger, Thomas; Heemann, Uwe; Koettgen, Anna; Arnold, Sebastian J.; Ozaltin, Fatih; Schmidts, Miriam; Hoefele, Julia 分享 收藏
Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells Baysal, Ipek; Yabanoglu-Ciftci, Samiye; Nemutlu, Emirhan; Eylem, Cemil Can; Gok-Topak, Elif Damla Go; Ulubayram, Kezban; Kir, Sedef; Gulhan, Bora; Ucar, Gulberk; Ozaltin, Fatih; Topaloglu, Rezan 分享 收藏
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schreuder, Michiel F.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Liu, Cuihua; Sun, Shuzhen; Deng, Fang; Wang, Xiaowen; Clave, Stephanie; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Schaefer, Franz 分享 收藏
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Zietkiewicz, Szymon; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schijvens, Anne M.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Deng, Fang; Rousset-Rouviere, Caroline; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Serna Higuita, Lina Maria; Schaefer, Franz; Trautmann, Agnes; Tabatabaeifar, Mansoureh; Gheissari, Alaleh; Hooman, Nakysa; Benetti, Elisa; Emma, Francesco; Nigmatullina, Nazym; Tkaczyk, Marcin; Borzecka, Halina; Tsygin, Alexey N.; Prikhodina, Larisa; Bogdanovic, Radovan; Mir, Sevgi; Fomina, Svitlana; Klopstock, Thomas; Prokisch, Holger; Kornblum, Cornelia; Liu, Cui-Hua; Sun, Shu-Zhen; Dong, Yang; Wang, Xiao-Wen; Luan, Jiang-Wei; Schaefer, Franz 分享 收藏
Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion Airik, Merlin; McCourt, Blake; Ozturk, Tugba Tastemel; Huynh, Amy B.; Zhang, Xiaoyi; Tometich, Justin T.; Topaloglu, Rezan; Ozen, Hasan; Orhan, Diclehan; Nejak-Bowen, Kari; Monga, Satdarshan P.; Hand, Timothy W.; Ozaltin, Fatih; Airik, Rannar 分享 收藏
An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis Emma, Francesco; van't Hoff, William; Hohenfellner, Katharina; Topaloglu, Rezan; Greco, Marcella; Ariceta, Gema; Bettini, Chiara; Bockenhauer, Detlef; Veys, Koenraad; Pape, Lars; Hulton, Sally; Collin, Suzanne; Ozaltin, Fatih; Servais, Aude; Deschenes, Georges; Novo, Robert; Bertholet-Thomas, Aurelia; Oh, Jun; Cornelissen, Elisabeth; Janssen, Mirian; Haffner, Dieter; Rava, Lucilla; Antignac, Corinne; Devuyst, Olivier; Niaudet, Patrick; Levtchenko, Elena 分享 收藏
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Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group (vol 17, pg 277, 2021) Boyer, Olivia; Schaefer, Franz; Haffner, Dieter; Bockenhauer, Detlef; Holtta, Tuula; Berody, Sandra; Webb, Hazel; Heselden, Marie; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Levtchenko, Elena; Vivarelli, Marina 分享 收藏
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Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group Boyer, Olivia; Schaefer, Franz; Haffner, Dieter; Bockenhauer, Detlef; Holtta, Tuula; Berody, Sandra; Webb, Hazel; Heselden, Marie; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Levtchenko, Elena; Vivarelli, Marina 分享 收藏
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Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group Lipska-Zietkiewicz, Beata Stefania; Ozaltin, Fatih; Holtta, Tuula; Bockenhauer, Detlef; Berody, Sandra; Levtchenko, Elena; Vivarelli, Marina; Webb, Hazel; Haffner, Dieter; Schaefer, Franz; Boyer, Olivia 分享 收藏
Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation (vol 88, pg 71, 2018) 对早期补充辅酶Q10的反应在CoQ2突变引起的CoQ10缺乏症中不持续 (第88卷，第71页，2018页) Eroglu, Fehime K.; Ozaltin, Fatih; Gonc, Nazli; Nalcacioglu, Hulya; Ozcakar, Z. Birsin; Yalnizoglu, Dilek; Gucer, Safak; Orhan, Diclehan; Eminoglu, Fatma Tuba; Gocmen, Rahsan; Alikasifoglu, Ayfer; Topaloglu, Rezan; Duzova, Ali 分享 收藏
An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues Akyol, Aytekin; Guner, Gunes; Ozseker, Havva Solak; Isik, Aynur; Atci, Ozge; Uzun, Sarp; Atayar, Emine; Ozaltin, Fatih; Gedikoglu, Gokhan; Sokmensuer, Cenk; Fearon, Eric R. 分享 收藏
Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation CoQ2突变引起的CoQ10缺乏症对早期补充辅酶Q10的反应不持续 Eroglu, Fehime K.; Ozaltin, Fatih; Gonc, Nazl; Nalcacioglu, Hulya; Ozcakar, Z. Birsin; Yalnizoglu, Dilek; Gucer, Safak; Orhan, Diclehan; Eminoglu, Fatma Tuba; Gocmen, Rahsan; Alikasifoglu, Ayfer; Topaloglu, Rezan; Duzova, Ali 分享 收藏
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