1. A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. Issue 4 (23rd September 2020) Authors: Saygili, Seha; Atayar, Emine; Canpolat, Nur; Elicevik, Mehmet; Kurugoglu, Sebuh; Sever, Lale; Caliskan, Salim; Ozaltin, Fatih Journal: Clinical genetics Issue: Volume 98:Issue 4(2020) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome. Issue 3 (7th January 2022) Authors: 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; Cali... Journal: Clinical genetics Issue: Volume 101:Issue 3(2022) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients: a cross-sectional web-based survey. Issue 5 (28th May 2021) Authors: Wente-Schulz, Sarah; Aksenova, Marina; Awan, Atif; Ambarsari, Cahyani Gita; Becherucci, Francesca; Emma, Francesco; Fila, Marc; Francisco, Telma; Gokce, Ibrahim; Gülhan, Bora; Hansen, Matthias; Jahnukainen, Timo; Kallash, Mahmoud; Kamperis, Konstantinos; Mason, Sherene; Mastrangelo, Antonio; Menc... Other Names: author non-byline.; Boyer Olivia author non-byline.; Buder Kathrin author non-byline.; Bulut İpek Kaplan author non-byline.; Cornelissen Elisabeth AM author non-byline.; Hernández Maria del Mar Espino author non-byline.; Hooman Nakysa author non-byline.; Kemper Markus author non-byline.; Maquet ... Journal: BMJ open Issue: Volume 11:Issue 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. MO026CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE. (29th May 2021) Authors: Tutal, Ozum; Gulhan, Bora; Atayar, Emine; Yuksel, Selcuk; Ozcakar, Z Birsin; Soylemezoglu, Oguz; Saygili, Seha; Inozu, Mihriban; Baskin, Esra; Duzova, Ali; Hayran, Mutlu; Topaloglu, Rezan; Ozaltin, Fatih Journal: Nephrology dialysis transplantation Issue: Volume 36(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Spatial Distribution of Macrophage Subtypes Among Rejection Subtypes in Renal Transplant Biopsies by Dual Immunohistochemistry. Issue 4 (23rd April 2023) Authors: Hurdogan, Ozge; Karakus, Fatmanur; Dirim, Ahmet Burak; Aksu, Bagdagul; Saygili, Seha; Turkmen, Aydin; Yilmaz, Alev; Canpolat, Nur; Solakoglu, Seyhun; Kilicaslan, Isin; Ozluk, Yasemin Journal: Applied immunohistochemistry & molecular morphology Issue: Volume 31:Issue 4(2023) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗