Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients

Por Besbas, Nesrin, Gulhan, Bora, Soylemezoglu, Oguz, Ozcakar, Z. Birsin, Korkmaz, Emine, Hayran, Mutlu, Ozaltin, Fatih
Publicado no BMC Nephrol (2017)

Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience

Por Topaloglu, Rezan, Orhan, Dicle, Bilginer, Yelda, Karabulut, Erdem, Ozaltin, Fatih, Duzova, Ali, Kale, Gulsev, Besbas, Nesrin
Publicado em 2013

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Por Hinkes, Bernward, Vlangos, Christopher, Heeringa, Saskia, Mucha, Bettina, Gbadegesin, Rasheed, Liu, Jinhong, Hasselbacher, Katrin, Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2008

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Por Chernin, Gil, Vega-Warner, Virginia, Schoeb, Dominik S., Heeringa, Saskia F., Ovunc, Bugsu, Saisawat, Pawaree, Cleper, Roxana, Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2010

Influence of Reduced Folate Carrier and Aminoimidazole Carboxamide Ribonucleotide Transformylase gene polymorphisms on the efficacy of methotrexate in juvenile idiopathic arthritis

Por Bilginer, Yelda, Utine, Eda, Kasapçopur, Özgür, Gülhan, Bora, Demirkaya, Erkan, Topaloğlu, Rezan, Düzova, Ali, Özaltın, Fatih, Alikaşifoğlu, Mehmet, Özen, Seza
Publicado em 2011

RESPIRATORY CHAIN DEFICIENCY PRESENTING AS DIFFUSE MESANGIAL SCLEROSIS WITH NPHS3 MUTATION

Por Baskin, Esra, Bayrakci, Umut Selda, Alehan, Füsun, Ozdemir, Handan, Oner, Ayse, Horvath, Rita, Hildebrandt, Friedhelm, Vega-Varner, V, Ozaltın, Fatih
Publicado em 2011

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Por Heeringa, Saskia F., Vlangos, Christopher N., Chernin, Gil, Hinkes, Bernward, Gbadegesin, Rasheed, Liu, Jinhong, Hoskins, Bethan E., Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2008

Genetic basis of cystinosis in Turkish patients: a single-center experience

Por Topaloglu, Rezan, Vilboux, Thierry, Coskun, Turgay, Ozaltin, Fatih, Tinloy, Brad, Gunay-Aygun, Meral, Bakkaloglu, Aysin, Besbas, Nesrin, van den Heuvel, Lambert, Kleta, Robert, Gahl, William A.
Publicado em 2011

Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD

Por Shroff, Rukshana, Aitkenhead, Helen, Costa, Nikola, Trivelli, Antonella, Litwin, Mieczyslaw, Picca, Stefano, Anarat, Ali, Sallay, Peter, Ozaltin, Fatih, Zurowska, Aleksandra, Jankauskiene, Augustina, Montini, Giovanni, Charbit, Marina, Schaefer, Franz, Wühl, Elke
Publicado no J Am Soc Nephrol (2016)

Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome

Por Ozaltin, Fatih, Ibsirlioglu, Tulin, Taskiran, Ekim Z., Baydar, Dilek Ertoy, Kaymaz, Figen, Buyukcelik, Mithat, Kilic, Beltinge Demircioglu, Balat, Ayse, Iatropoulos, Paraskevas, Asan, Esin, Akarsu, Nurten A., Schaefer, Franz, Yilmaz, Engin, Bakkaloglu, Ayşin
Publicado em 2011

Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD

Por Taskiran, Ekim Z., Korkmaz, Emine, Gucer, Safak, Kosukcu, Can, Kaymaz, Figen, Koyunlar, Cansu, Bryda, Elizabeth C., Chaki, Moumita, Lu, Dongmei, Vadnagara, Komal, Candan, Cengiz, Topaloglu, Rezan, Schaefer, Franz, Attanasio, Massimo, Bergmann, Carsten, Ozaltin, Fatih
Publicado em 2014

Circulating suPAR in Two Cohorts of Primary FSGS

Por Wei, Changli, Trachtman, Howard, Li, Jing, Dong, Chuanhui, Friedman, Aaron L., Gassman, Jennifer J., McMahan, June L., Radeva, Milena, Heil, Karsten M., Trautmann, Agnes, Anarat, Ali, Emre, Sevinc, Ghiggeri, Gian M., Ozaltin, Fatih, Haffner, Dieter, Gipson, Debbie S., Kaskel, Frederick, Fischer, Dagmar-Christiane, Schaefer, Franz, Reiser, Jochen
Publicado em 2012

ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS

Por Korkmaz, Emine, Lipska-Ziętkiewicz, Beata S., Boyer, Olivia, Gribouval, Olivier, Fourrage, Cecile, Tabatabaei, Mansoureh, Schnaidt, Sven, Gucer, Safak, Kaymaz, Figen, Arici, Mustafa, Dinckan, Ayhan, Mir, Sevgi, Bayazit, Aysun K., Emre, Sevinc, Balat, Ayse, Rees, Lesley, Shroff, Rukshana, Bergmann, Carsten, Mourani, Chebl, Antignac, Corinne, Ozaltin, Fatih, Schaefer, Franz
Publicado no J Am Soc Nephrol (2016)

Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

Por Gee, Heon Yung, Ashraf, Shazia, Wan, Xiaoyang, Vega-Warner, Virginia, Esteve-Rudd, Julian, Lovric, Svjetlana, Fang, Humphrey, Hurd, Toby W., Sadowski, Carolin E., Allen, Susan J., Otto, Edgar A., Korkmaz, Emine, Washburn, Joseph, Levy, Shawn, Williams, David S., Bakkaloglu, Sevcan A., Zolotnitskaya, Anna, Ozaltin, Fatih, Zhou, Weibin, Hildebrandt, Friedhelm
Publicado em 2014

Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE(2) production

Por Zhu, Jili, Chaki, Moumita, Lu, Dongmei, Ren, Chongyu, Wang, Shan-Shan, Rauhauser, Alysha, Li, Binghua, Zimmerman, Susan, Jun, Bokkyoo, Du, Yong, Vadnagara, Komal, Wang, Hanquin, Elhadi, Sarah, Quigg, Richard J., Topham, Matthew K., Mohan, Chandra, Ozaltin, Fatih, Zhou, Xin J., Marciano, Denise K., Bazan, Nicolas G., Attanasio, Massimo
Publicado no Am J Physiol Renal Physiol (2016)

MYO1E MUTATIONS AND CHILDHOOD FAMILIAL FOCAL SEGMENTAL GLOMERULOSCLEROSIS

Por Mele, Caterina, Iatropoulos, Paraskevas, Donadelli, Roberta, Calabria, Andrea, Maranta, Ramona, Cassis, Paola, Buelli, Simona, Tomasoni, Susanna, Piras, Rossella, Krendel, Mira, Bettoni, Serena, Morigi, Marina, Delledonne, Massimo, Pecoraro, Carmine, Abbate, Isabella, Capobianchi, Maria Rosaria, Hildebrandt, Friedhelm, Otto, Edgar, Schaefer, Franz, Macciardi, Fabio, Ozaltin, Fatih, Emre, Sevinc, Ibsirlioglu, Tulin, Benigni, Ariela, Remuzzi, Giuseppe, Noris, Marina
Publicado em 2011

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Por Braun, Daniela A., Schueler, Markus, Halbritter, Jan, Gee, Heon Yung, Porath, Jonathan D., Lawson, Jennifer A., Airik, Rannar, Shril, Shirlee, Allen, Susan J., Stein, Deborah, Al Kindy, Adila, Beck, Bodo B., Cengiz, Nurcan, Moorani, Khemchand N., Ozaltin, Fatih, Hashmi, Seema, Sayer, John A., Bockenhauer, Detlef, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Hildebrandt, Friedhelm
Publicado no Kidney Int (2016)

Mutations in nuclear pore genes NUP93, NUP205, and XPO5 cause steroid resistant nephrotic syndrome

Por Braun, Daniela A., Sadowski, Carolin E., Kohl, Stefan, Lovric, Svjetlana, Astrinidis, Susanne A., Pabst, Werner L., Gee, Heon Yung, Ashraf, Shazia, Lawson, Jennifer A., Shril, Shirlee, Airik, Merlin, Tan, Weizhen, Schapiro, David, Rao, Jia, Choi, Won-Il, Hermle, Tobias, Kemper, Markus J., Pohl, Martin, Ozaltin, Fatih, Konrad, Martin, Bogdanovic, Radovan, Büscher, Rainer, Helmchen, Udo, Serdaroglu, Erkin, Lifton, Richard P., Antonin, Wolfram, Hildebrandt, Friedhelm
Publicado no Nat Genet (2016)

DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN

Por Ozaltin, Fatih, Li, Binghua, Rauhauser, Alysha, An, Sung-Wan, Soylemezoglu, Oguz, Gonul, Ipek Isik, Taskiran, Ekim Z., Ibsirlioglu, Tulin, Korkmaz, Emine, Bilginer, Yelda, Duzova, Ali, Ozen, Seza, Topaloglu, Rezan, Besbas, Nesrin, Ashraf, Shazia, Du, Yong, Liang, Chaoying, Chen, Phylip, Lu, Dongmei, Vadnagara, Komal, Arbuckle, Susan, Lewis, Deborah, Wakeland, Benjamin, Quigg, Richard J., Ransom, Richard F., Wakeland, Edward K., Topham, Matthew K., Bazan, Nicolas G., Mohan, Chandra, Hildebrandt, Friedhelm, Bakkaloglu, Aysin, Huang, Chou-Long, Attanasio, Massimo
Publicado em 2013

Spectrum of Steroid-Resistant and Congenital Nephrotic Syndrome in Children: The PodoNet Registry Cohort

Por Trautmann, Agnes, Bodria, Monica, Ozaltin, Fatih, Gheisari, Alaleh, Melk, Anette, Azocar, Marta, Anarat, Ali, Caliskan, Salim, Emma, Francesco, Gellermann, Jutta, Oh, Jun, Baskin, Esra, Ksiazek, Joanna, Remuzzi, Giuseppe, Erdogan, Ozlem, Akman, Sema, Dusek, Jiri, Davitaia, Tinatin, Özkaya, Ozan, Papachristou, Fotios, Firszt-Adamczyk, Agnieszka, Urasinski, Tomasz, Testa, Sara, Krmar, Rafael T., Hyla-Klekot, Lidia, Pasini, Andrea, Özcakar, Z. Birsin, Sallay, Peter, Cakar, Nilgun, Galanti, Monica, Terzic, Joelle, Aoun, Bilal, Caldas Afonso, Alberto, Szymanik-Grzelak, Hanna, Lipska, Beata S., Schnaidt, Sven, Schaefer, Franz
Publicado no Clin J Am Soc Nephrol (2015)