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The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study.
Published in:
Nephron, 2024, v. 148, n. 5, p. 319, doi. 10.1159/000528258
By:
- Tutal, Ozum;
- Gulhan, Bora;
- Atayar, Emine;
- Yuksel, Selcuk;
- Ozcakar, Z. Birsin;
- Soylemezoglu, Oguz;
- Saygili, Seha;
- Caliskan, Salim;
- Inozu, Mihriban;
- Baskin, Esra;
- Duzova, Ali;
- Hayran, Mutlu;
- Topaloglu, Rezan;
- Ozaltin, Fatih
Publication type:
Article
The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome.
Published in:
Turkish Journal of Pediatrics, 2023, v. 65, n. 3, p. 456, doi. 10.24953/turkjped.2022.735
By:
- Özdemir, Gülşah;
- Gülhan, Bora;
- Şükür, Eda Didem Kurt;
- Atayar, Emine;
- Atan, Raziye;
- Dursun, İsmail;
- Özçakar, Zeynep Birsin;
- Saygılı, Seha;
- Soylu, Alper;
- Söylemezoğlu, Oğuz;
- Yılmaz, Alev;
- Bayazıt, Aysun Karabay;
- Eroğlu, Fehime Kara;
- Demir, Belde Kasap;
- Yüksel, Selçuk;
- Tabel, Yılmaz;
- Ağbaş, Ayşe;
- Düzova, Ali;
- Hayran, Mutlu;
- Özaltın, Fatih
Publication type:
Article
Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?
Published in:
Turkish Journal of Pediatrics, 2021, v. 63, n. 6, p. 986, doi. 10.24953/turkjped.2021.06.006
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
Publication type:
Article
Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation.
Published in:
Turkish Journal of Pediatrics, 2019, v. 61, n. 5, p. 657, doi. 10.24953/turkjped.2019.05.003
By:
- Atmaca, Mustafa;
- Gülhan, Bora;
- Atayar, Emine;
- Bayazıt, Aysun Karabay;
- Candan, Cengiz;
- Arıcı, Mustafa;
- Topaloğlu, Rezan;
- Özaltın, Fatih
Publication type:
Article
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.
Published in:
Clinical Genetics, 2022, v. 101, n. 3, p. 346, doi. 10.1111/cge.14105
By:
- Canpolat, Nur;
- Liu, Dingxiao;
- Atayar, Emine;
- Saygili, Seha;
- Kara, Nazli Sila;
- Westfall, Trudi A.;
- Ding, Qiong;
- Brown, Bartley J.;
- Braun, Terry A.;
- Slusarski, Diane;
- Karli Oguz, Kader;
- Ozluk, Yasemin;
- Tuysuz, Beyhan;
- Tastemel Ozturk, Tugba;
- Sever, Lale;
- Sezerman, Osman Ugur;
- Topaloglu, Rezan;
- Caliskan, Salim;
- Attanasio, Massimo;
- Ozaltin, Fatih
Publication type:
Article
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
Published in:
Clinical Genetics, 2020, v. 98, n. 4, p. 390, doi. 10.1111/cge.13813
By:
- Saygili, Seha;
- Atayar, Emine;
- Canpolat, Nur;
- Elicevik, Mehmet;
- Kurugoglu, Sebuh;
- Sever, Lale;
- Caliskan, Salim;
- Ozaltin, Fatih
Publication type:
Article
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
Published in:
Pediatric Nephrology, 2020, v. 35, n. 10, p. 1941, doi. 10.1007/s00467-020-04574-8
By:
- Ozdemir, Gulsah;
- Gulhan, Bora;
- Atayar, Emine;
- Saygılı, Seha;
- Soylemezoglu, Oguz;
- Ozcakar, Zeynep Birsin;
- Eroglu, Fehime Kara;
- Candan, Cengiz;
- Demir, Belde Kasap;
- Soylu, Alper;
- Yüksel, Selçuk;
- Alpay, Harika;
- Agbas, Ayse;
- Duzova, Ali;
- Hayran, Mutlu;
- Ozaltin, Fatih;
- Topaloglu, Rezan
Publication type:
Article
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers.
Published in:
Pediatric Nephrology, 2019, v. 34, n. 1, p. 77, doi. 10.1007/s00467-018-3982-7
By:
- Saygili, Seha;
- Canpolat, Nur;
- Sever, Lale;
- Caliskan, Salim;
- Atayar, Emine;
- Ozaltin, Fatih
Publication type:
Article
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions.
Published in:
2019
By:
- Saygili, Seha;
- Canpolat, Nur;
- Sever, Lale;
- Caliskan, Salim;
- Atayar, Emine;
- Ozaltin, Fatih
Publication type:
Case Study

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