Fatih Ozaltin
Hacettepe Üniversitesi
H-index: 49
Asia-Turkey
Top articles of Fatih Ozaltin
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Genotype/phenotype relationship in mild congenital nephrotic syndrome | Srpski arhiv za celokupno lekarstvo | Bilsana Mulić Amira Peco-Antić Fatih Ozaltin | 2024 |
Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience | Pediatric Nephrology | Tugba Tastemel Ozturk Ali Düzova Pembe Derin Oygar Demet Baltu Pelin Ozcilingir Hakverdi | 2024/3 |
Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells | Laboratory Investigation | İpek Baysal Samiye Yabanoglu-Ciftci Emirhan Nemutlu Cemil Can Eylem Elif Damla Gök-Topak | 2024/1/1 |
Management of pediatric hemolytic uremic syndrome | Bora Gülhan Fatih Özaltın Kibriya Fidan Zeynep Birsin Özçakar Oğuz Söylemezoğlu | 2024/2/28 | |
COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much? | Klinische Pädiatrie | Demet Baltu Eda Didem Kurt-Sukur Tugba Tastemel Ozturk Bora Gulhan Fatih Ozaltin | 2024/1/15 |
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence | Kidney International Reports | Jessica Kachmar Olivia Boyer Beata Lipska-Ziętkiewicz Vincent Morinière Olivier Gribouval | 2024/1/10 |
Odnos između genotipa i fenotipa u blagom kongenitalnom nefrotskom sindromu | Srpski arhiv za celokupno lekarstvo | Bilsana Mulić Amira Peco-Antić Fatih Ozaltin | 2024/1 |
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) | Kidney international | Korbinian M Riedhammer Thanh-Minh T Nguyen Can Koşukcu Julia Calzada-Wack Yong Li | 2024/4/1 |
The clinical and mutational spectrum of 69 turkish children with autosomal recessive or autosomal dominant polycystic kidney disease: a multicenter retrospective cohort study | Nephron | Ozum Tutal Bora Gulhan Emine Atayar Selcuk Yuksel Z Birsin Ozcakar | 2023/1/19 |
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) | medRxiv | Korbinian M Riedhammer Thanh-Minh T Nguyen Can Koşukcu Julia Calzada-Wack Yong Li | 2023/3/22 |
COVID‐19 associated thrombotic microangiopathy | Nephrology | Esra Karabag Yilmaz Memnune Nur Cebi Iremnaz Karahan Seha Saygılı Ruveyda Gulmez | 2023/10 |
Çocukluk Çağı Böbrek Hastalıklarında Genetik Testler: Kime, Ne Zaman? | Turkiye Klinikleri Pediatric Nephrology-Special Topics | Eda Didem KURT ŞÜKÜR Fatih ÖZALTIN | 2023 |
HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract | Pediatric Nephrology | Seha Saygili Salim Caliskan Fatih Ozaltin | 2023/3 |
Albuminuria is associated with 24-hour and night-time diastolic blood pressure in urinary tract infection with renal scarring | The Turkish journal of pediatrics | Demet Baltu Bilge Volkan Salancı Bora Gülhan Fatih Özaltın Ali Düzova | 2023/8/25 |
An unusual cause of diarrhea in a child with nephrotic syndrome: Questions | Pediatric Nephrology | Demet Baltu Eda Didem Kurt Sukur Ersin Gumus Tugba Tastemel Ozturk Yasin Maruf Ergen | 2023/12 |
Hemoglobin cast nephropathy: a rare but serious complication of hemolysis in a pediatric patient | Turkish Journal of Pediatrics | Demet Baltu Nihan Oral Selman Kesici Rezan Topaloğlu OSMAN ÖZCEBE | 2023 |
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature | Tugba Tastemel Ozturk Nur Canpolat Seha Saygili Umut Selda Bayrakci Oguz Soylemezoglu | 2023/3 | |
COVID-19 associated thrombotic microangiopathy. | Nephrology (Carlton, Vic.) | MN Cebi I Karahan S Saygılı R Gulmez EB Demirgan | 2023/7/23 |
A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT) | Clinical Genetics | Seha Saygılı Can Koşukcu Turgut Baştuğ Özlem Akgün Doğan Esra Karabağ Yılmaz | 2023/12 |
The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome | Turkish Journal of Pediatrics | EMINE OZDEMIR Bora Gülhan Eda Şükür Emine Atayar Raziye Atan | 2023 |
