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Seha Kamil Saygılı (Seha Saygılı, Seha Saygili)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 15

Top Venues

Pediatric nephrology (Berlin, Germany)

Clinical genetics

Pediatric research

Turkish journal of medical sciences

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

Publications

Esra Karabag Yilmaz, Memnune Nur Cebi, Iremnaz Karahan, Seha Kamil Saygılı, Ruveyda Gulmez, Ebru Burcu Demirgan, Cansu Durak, Fatih Aygun, Fatih Ozaltin, Salim Caliskan, Nur Canpolat
COVID-19 associated thrombotic microangiopathy. Nephrology (Carlton, Vic.) (2023)
Neslihan Günay, İsmail Dursun, Ibrahim Gokce, Mehtap Akbalik Kara, Demet Tekcan, Neslihan Çiçek, Meral Torun Bayram, Mustafa Koyun, Nida Dinçel, Hasan Dursun, Seha Kamil Saygılı, Zeynep Nagehan Yürük Yıldırım, Selcuk Yuksel, Osman Dönmez, Sibel Yel, Beltinge Demircioğlu Kılıç, Özlem Aydoğ, Bahriye Atmis, Aysun Çaltık Yılmaz, Sevcan A Bakkaloglu, Mehmet Baha Aytaç, Mehmet Tasdemir, Belde Kasap-Demir, Alper Soylu, Elif Çomak, Aslı Kantar Özşahin, Alper Kaçar, Nur Canpolat, Alev Yilmaz, İlknur Girişgen, Kadirye Betül Akkoyunlu, Harika Alpay, Muammer Hakan Poyrazoğlu
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil? Pediatric nephrology (Berlin, Germany) (2023)
Seha Kamil Saygılı, 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)
Seha Kamil Saygılı, 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 Saygılı, 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 Saygılı, 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)
Esra Karabag Yilmaz, Seha Kamil Saygılı, 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)
Ruveyda Gulmez, Doğukan Özbey, Ayşe Ağbaş, Bagdagul Aksu, Nurdan Yıldız, Diana Üçkardeş, Seha Kamil Saygılı, Esra Karabag Yilmaz, Zeynep Nagehan Yürük Yıldırım, Mehmet Tasdemir, Ayça Kiykim, Haluk Cezmi Cokugras, Nur Canpolat, Ahmet Nayir, Bekir Sami Kocazeybek, Salim Caliskan
Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children. Pediatric nephrology (Berlin, Germany) (2022)
Seha Kamil Saygılı, Nur Canpolat, Rumeysa Yasemin Cicek, Ayse Agbas, Esra Karabag Yilmaz, Ayse Ayzit Kilinc Sakalli, Deniz Aygun, Gülsen Akkoc, Kaan Can Demirbas, Dildar Konukoglu, Haluk Cokugras, Salim Caliskan, Lale Sever
Clinical and subclinical acute kidney injury in children with mild-to-moderate COVID-19. Pediatric research (2022)
Ilayda Altun, Seha Kamil Saygılı, Nur Canpolat, Yasemin Ozluk, Ozge Hurdogan, Gozde Yesil Sayın, Salim Caliskan, Fatma Lale Sever
Strong mesangial IgA staining-does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Answers. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Mehmet Tasdemir, Nur Canpolat, Nurdan Yıldız, Gul Ozcelik, Meryem Benzer, Seha Kamil Saygılı, Emine Neşe Özkayin, Özde Nisa Türkkan, Ayse Balat, Cengiz Candan, Mehtap Çelakıl, Sevgi Yavuz, Nurver Akıncı, Nilüfer Göknar, Cihangir Akgün, Sebahat Tülpar, Harika Alpay, Fatma Lale Sever, Ilmay Bilge
Rituximab treatment for difficult-to-treat nephrotic syndrome in children: a multicenter, retrospective study Turkish journal of medical sciences 51 (4) (2021)
Ilayda Altun, Seha Kamil Saygılı, Nur Canpolat, Yasemin Ozluk, Ozge Hurdogan, Gozde Yesil Sayın, Salim Caliskan, Fatma Lale Sever
Strong mesangial IgA staining-does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Questions. Pediatric nephrology (Berlin, Germany) 36 (7) (2021)
Seha Kamil Saygılı, 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)
Seha Kamil Saygılı, Nur Canpolat, Aydilek Dagdeviren Cakir, Dildar Konukoglu, Hande Turan, Salim Caliskan, Oya Ercan, Saadet Olcay Evliyaoglu, Fatma Lale Sever
Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar? Pediatric nephrology (Berlin, Germany) 35 (7) (2020)
Seha Kamil Saygılı, Nur Canpolat, Lale Sever, Salim Caliskan, Emine Atayar, Fatih Ozaltin
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions. Pediatric nephrology (Berlin, Germany) 34 (1) (2018)

Seha Kamil Saygılı.css-eqlu8i{font-size:small;padding-left:4px;} (Seha Saygılı, Seha Saygili)

Publication Activity (10 Years)

Top Topics

Top Venues

Seha Kamil Saygılı (Seha Saygılı, Seha Saygili)