Seha Saygili
Overview
Explore the profile of Seha Saygili including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
53
Citations
139
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Demirbas K, Saygili S, Yilmaz E, Gulmez R, Agbas A, Tasdemir M, et al.
Pediatr Transplant
. 2025 Mar;
29(3):e70068.
PMID: 40078030
Background: Education and enhancing the knowledge of adolescents who will undergo kidney transplantation are among the primary objectives of their care. While there are specific interventions in place to achieve...
2.
Yilmaz G, Saygili S, Agbas A, Yilmaz E, Varis A, Canpolat N
Front Microbiol
. 2025 Feb;
16:1499813.
PMID: 39949623
Introduction: This study aimed to compare the gut microbiota composition in pediatric kidney transplant (KTx) recipient with that of healthy children. Methods: This cross-sectional observational study included 30 pediatric KTx...
3.
Hasturk B, Agbas A, Akgun-Dogan O, Yilmaz E, Saygili S, Beser O, et al.
Pediatr Nephrol
. 2025 Jan;
PMID: 39869206
Autosomal recessive proximal renal tubular acidosis (AR-pRTA) with ocular abnormalities is a rare syndrome caused by variants in the SLC4A4 gene, which encodes Na/HCO3 cotransporter (NBCe1). The syndrome primarily affects...
4.
Demirbas K, Cakmak C, Saygili S, Canpolat N, Kasapcopur O
Balkan Med J
. 2025 Jan;
PMID: 39780662
No abstract available.
5.
Gharagozlou S, Wright N, Murguia-Favela L, Eshleman J, Midgley J, Saygili S, et al.
Adv Biol Regul
. 2024 Oct;
94:101058.
PMID: 39454238
Sphingosine phosphate lyase insufficiency syndrome (SPLIS) is a genetic disease associated with renal, endocrine, neurological, skin and immune defects. SPLIS is caused by inactivating mutations in SGPL1, which encodes sphingosine...
6.
Gulmez R, Saygili S, Yilmaz E, Agbas A, Canpolat N
Pediatr Nephrol
. 2024 Sep;
40(3):707-709.
PMID: 39347990
Despite its widespread use in patients undergoing organ transplantation or managing nephrotic syndrome, there is a lack of literature on the acute toxicity of cyclosporine A (CsA). This report presents...
7.
Yilmaz E, Saygili S, Musayeva G, Gulmez R, Agbas A, Ozluk Y, et al.
Turk J Pediatr
. 2024 Mar;
66(1):128-133.
PMID: 38523389
Background: Relapses or new-onset IgA nephropathy (IgAN) have been documented in patients after vaccination against SARS-CoV-2; however, only one adult patient has been reported in whom pre-existing IgAN worsened during...
8.
Yilmaz K, Saygili S, Canpolat N, Akgun-Dogan O, Yuruk Yildirim Z, Cicek-Oksuz R, et al.
Front Pediatr
. 2024 Mar;
12:1357365.
PMID: 38464892
Introduction: In the pediatric context, most children with autosomal dominant polycystic kidney disease (ADPKD) maintain a normal glomerular filtration rate (GFR) despite underlying structural kidney damage, highlighting the critical need...
9.
Demirbas K, Yildiz M, Saygili S, Canpolat N, Kasapcopur O
Turk Arch Pediatr
. 2024 Mar;
59(2):121-130.
PMID: 38454219
In this era of rapidly advancing technology, artificial intelligence (AI) has emerged as a transformative force, even being called the Fourth Industrial Revolution, along with gene editing and robotics. While...
10.
Bakkaloglu S, Delibas A, Surmeli Doven S, Taner S, Yavuz S, Erfidan G, et al.
Nephrol Dial Transplant
. 2024 Feb;
39(9):1514-1522.
PMID: 38327222
Background: Two earthquakes on 6 February 2023 destroyed 10 cities in Türkiye. We report our experience with pediatric victims during these catastrophes, with a focus on crush syndrome related-acute kidney...