Fatih Ozaltin (Fatih Özaltın, Fatih Ozaltın)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 29

Top Topics

Ejection Fraction

Long Noncoding Rna

Roux En Y Gastric Bypass

Top Venues

Pediatric nephrology (Berlin, Germany)

Pediatric transplantation

International journal of molecular sciences

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Yagmur Unsal, Demet Baltu, Bora Gülhan, Fatma Visal Okur, Fatih Ozaltin, Ali Düzova, Rezan Topaloğlu, Zeynep Alev Ozon, Elmas Nazlı Gonç
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. Pediatric transplantation 28 (4) (2024)
Yagmur Unsal, Demet Baltu, Bora Gülhan, Fatma Visal Okur, Fatih Ozaltin, Ali Düzova, Rezan Topaloğlu, Zeynep Alev Ozon, Elmas Nazlı Gonç
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. Pediatric transplantation 28 (4) (2024)
Yagmur Unsal, Demet Baltu, Bora Gülhan, Fatma Visal Okur, Fatih Ozaltin, Ali Düzova, Rezan Topaloğlu, Zeynep Alev Ozon, Elmas Nazlı Gonç
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. Pediatric transplantation 28 (4) (2024)
Esra Karabag Yilmaz, Nur Memnune Cebi, Iremnaz Karahan, Seha Kamil Saygili, Ruveyda Gulmez, Ebru Burcu Demirgan, Cansu Durak, Fatih Aygun, Fatih Ozaltin, Salim Caliskan, Nur Canpolat
COVID-19 associated thrombotic microangiopathy. Nephrology (Carlton, Vic.) (2023)
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
An unusual cause of diarrhea in a child with nephrotic syndrome: Questions. Pediatric nephrology (Berlin, Germany) (2023)
Emirhan Nemutlu, Fatih Ozaltin, Samiye Yabanoglu-Ciftci, Bora Gulhan, Cemil Can Eylem, İpek Baysal, Elif Damla Gök-Topak, Kezban Ulubayram, Osman Ugur Sezerman, Gülberk Uçar, Sedef Kır, Rezan Topaloglu
Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis. International journal of molecular sciences 24 (3) (2023)
Tugba Tastemel Ozturk, Ali Düzova, Pembe Derin Oygar, Demet Baltu, Pelin Ozcilingir Hakverdi, Sibel Lacinel Gurlevik, Eda Didem Kurt Sukur, Hakan Hayrettin Aykan, Seher Sener, İlker Ertuğrul, Selman Kesici, Bora Gülhan, Fatih Ozaltin, Yasemin Özsürekci, Ali Bulent Cengiz, Rezan Topaloğlu
Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience. Pediatric nephrology (Berlin, Germany) (2023)
Emirhan Nemutlu, Fatih Ozaltin, Samiye Yabanoglu-Ciftci, Bora Gulhan, Cemil Can Eylem, İpek Baysal, Elif Damla Gök-Topak, Kezban Ulubayram, Osman Ugur Sezerman, Gülberk Uçar, Sedef Kır, Rezan Topaloglu
Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis. International journal of molecular sciences 24 (3) (2023)
Demet Baltu, Eda Didem Kurt Sukur, Ersin Gumus, Tugba Tastemel Ozturk, Yasin Maruf Ergen, Duygu Demirtas, Bora Gülhan, Fatih Ozaltin, Diclehan Orhan, Hasan Özen, Ali Düzova
An unusual cause of diarrhea in a child with nephrotic syndrome: Answers. Pediatric nephrology (Berlin, Germany) (2023)
Seha Kamil Saygili, Can Koşukcu, Turgut Baştuğ, Özlem Akgün Doğan, Esra Karabağ Yılmaz, Ayşe Uçar Kalyoncu, Ayşe Ağbaş, Nur Canpolat, Salim Çalışkan, Fatih Ozaltin
A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT). Clinical genetics (2023)
Emirhan Nemutlu, Fatih Ozaltin, Samiye Yabanoglu-Ciftci, Bora Gulhan, Cemil Can Eylem, İpek Baysal, Elif Damla Gök-Topak, Kezban Ulubayram, Osman Ugur Sezerman, Gülberk Uçar, Sedef Kır, Rezan Topaloglu
Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis. International journal of molecular sciences 24 (3) (2023)
Seha Kamil Saygili, Salim Caliskan, Fatih Ozaltin
HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract. Pediatric nephrology (Berlin, Germany) (2022)
Tugba Tastemel Ozturk, Nur Canpolat, Seha Kamil Saygili, Umut Selda Bayrakci, H Oğuz Söylemezoğlu, Fatih Ozaltin, Rezan Topaloğlu
A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature. Pediatric nephrology (Berlin, Germany) (2022)
Nur Canpolat, Dingxiao Liu, Emine Atayar, Seha Kamil Saygili, Nazli Sila Kara, Trudi A Westfall, Qiong Ding, Bartley J Brown, Terry A Braun, Diane C Slusarski, Kader Karlı Oğuz, Yasemin Ozluk, Beyhan Tüysüz, Tugba Tastemel Ozturk, Fatma Lale Sever, Osman Ugur Sezerman, Rezan Topaloğlu, Salim Caliskan, Massimo Attanasio, Fatih Ozaltin
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome. Clinical genetics 101 (3) (2022)
Seher Şener, Özge Basaran, Ezgi Deniz Batu, Erdal Atalay, Saliha Esenboga, Deniz Çağdaş Ayvaz, Bulent Baris Kuskonmaz, Yelda Bilginer, Fatih Ozaltin, Berna Oguz, Ali Düzova, F İlhan Tezcan, Seher Sener
Childhood-onset Takayasu arteritis and immunodeficiency: case-based review. Clinical rheumatology 41 (9) (2022)
Esra Karabag Yilmaz, Seha Kamil Saygili, Bora Gülhan, Nur Canpolat, Aysun Karabay Bayazıt, Beltinge Demircioğlu Kiliç, Nurver Akıncı, Meryem Benzer, Nilüfer Göknar, Asli Kavaz Tufan, Mukaddes Kalyoncu, Hulya Nalcacioglu, Demet Tekcan, Gizem Yildiz, Ayşe Ağbaş, Ahmet Nayir, Rezan Topaloğlu, Salim Caliskan, Fatih Ozaltin
A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability. Pediatric nephrology (Berlin, Germany) 37 (8) (2022)
Tugba Tastemel Ozturk, Fatih Ozaltin, Rezan Topaloğlu
Response to Dr. Spizzirri et al. Pediatric nephrology (Berlin, Germany) (2022)
Olivia Boyer, Franz Schaefer, Dieter Haffner, Detlef Bockenhauer, Tuula Hölttä, Sandra Bérody, Hazel Webb, Marie Heselden, Beata Stefania Lipska-Ziętkiewicz, Fatih Ozaltin, Elena Levtchenko, Marina Vivarelli
Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group. Nature reviews. Nephrology 17 (4) (2021)
Tugba Tastemel Ozturk, Demet Baltu, Eda Didem Kurt Sukur, Yasemin Özsürekci, Kadri Safak Gucer, Özge Basaran, Bora Gülhan, Fatih Ozaltin, Ali Düzova, Rezan Topaloğlu
Acute kidney injury in a patient with COVID-19: Answers. Pediatric nephrology (Berlin, Germany) 36 (12) (2021)
Tugba Tastemel Ozturk, Demet Baltu, Eda Didem Kurt Sukur, Yasemin Özsürekci, Kadri Safak Gucer, Özge Basaran, Bora Gülhan, Fatih Ozaltin, Ali Düzova, Rezan Topaloğlu
Acute kidney injury in a patient with COVID-19: Questions. Pediatric nephrology (Berlin, Germany) 36 (12) (2021)
Seha Kamil Saygili, Emine Atayar, Nur Canpolat, Mehmet Elicevik, Sebuh Kurugoglu, Lale Sever, Salim Caliskan, Fatih Ozaltin
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. Clinical genetics 98 (4) (2021)
Zeynep Birsin Özçakar, Fatih Ozaltin, Bora Gülhan, Elif Çomak, Gönül Parmaksız, Esra Baskın, Rezan Topaloğlu, Belde Kasap-Demir, Nur Canpolat, Zeynep Nagehan Yuruk Yildirim, Beltinge Demircioğlu Kiliç, Selçuk Yüksel, H Oğuz Söylemezoğlu
Transplantation in pediatric aHUS within the era of eculizumab therapy. Pediatric transplantation 25 (3) (2020)
Selcuk Yuksel, İpek Işık Gönül, Nur Canpolat, İbrahim Gökçe, Sare Gülfem Özlü, Zeynep Birsin Özçakar, Fatih Ozaltin, Oğuz Söylemezoğlu
Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 23 (5) (2020)
Beata Stefania Lipska-Ziętkiewicz, Fatih Ozaltin, Tuula Hölttä, Detlef Bockenhauer, Sandra Bérody, Elena Levtchenko, Marina Vivarelli, Hazel Webb, Dieter Haffner, Franz Schaefer, Olivia Boyer
Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group. European journal of human genetics : EJHG 28 (10) (2020)
Tülin Güngör, Fehime Kara Eroğlu, Evrim Kargın Çakıcı, Fatma Yazılıtaş, Gökçe Can, Evra Çelikkaya, Deniz Karakaya, Eda Didem Kurt Şükür, Fatih Ozaltin, Beytullah Yağız, Mehmet Bülbül
Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence? Acta clinica Belgica 76 (2) (2019)
Aytekin Akyol, Günes Güner, Havva Solak Özşeker, Aynur Işık, Özge Atcı, Sarp Uzun, Emine Atayar, Fatih Ozaltin, Gökhan Gedikoğlu, Cenk Sökmensüer, Eric R Fearon
An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues. Laboratory investigation; a journal of technical methods and pathology 99 (1) (2018)
Mustafa Atmaca, Bora Gulhan, Emine Korkmaz, Mihriban Inozu, Oguz Soylemezoglu, Cengiz Candan, Aysun Karabay Bayazıt, Ahmet Midhat Elmacı, Gonul Parmaksiz, Ali Duzova, Nesrin Besbas, Rezan Topaloglu, Fatih Ozaltin
Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment. Pediatric nephrology (Berlin, Germany) 32 (8) (2017)
Gozdem Kayki, Davut Bozkaya, Fatih Ozaltin, Diclehan Orhan, Figen Kaymaz, Emine Korkmaz, Sule Yigit
Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4. Fetal and pediatric pathology 36 (4) (2017)
Nesrin Besbas, Bora Gulhan, Oguz Soylemezoglu, Z Birsin Ozcakar, Emine Korkmaz, Mutlu Hayran, Fatih Ozaltin
Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients. BMC nephrology 18 (1) (2017)