Sebuh Kurugoglu
Overview
Explore the profile of Sebuh Kurugoglu including associated specialties, affiliations and a list of published articles.
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52
Citations
228
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Recent Articles
1.
Gunes N, Alkaya D, Kurugoglu S, Ozyalvac N, Bursali A, Elcioglu N, et al.
Pediatr Radiol
. 2025 Jan;
55(3):505-519.
PMID: 39825918
Background: Heterozygous TRPV4 mutations cause a group of skeletal dysplasias characterized by short stature, short trunk, and skeletal deformities. Objective: The aim of this study is to compare the natural...
2.
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...
3.
Gok A, Saygili S, Kurugoglu S, Saltik S, Canpolat N
Pediatr Neurol
. 2023 Nov;
150:32-36.
PMID: 37951159
Background: Nephrolithiasis is not a well-documented condition in children with spinal muscular atrophy (SMA). It is possible that this condition was underestimated before the era of nusinersen because of a...
4.
Gunes N, Alkaya D, Toylu A, Ozudogru P, Cifci Sunamak E, Seker A, et al.
Turk Arch Pediatr
. 2023 Jun;
58(4):376-381.
PMID: 37317574
Objective: Hereditary multiple osteochondromas is an autosomal dominant disorder caused by heterozygous pathogenic variants in EXT1 or EXT2. We aimed to evaluate the clinical and molecular findings of a Turkish...
5.
Tuysuz B, Alkaya D, Geyik F, Alaylioglu M, Kasap B, Kurugoglu S, et al.
J Med Genet
. 2022 Dec;
60(8):819-826.
PMID: 36543534
Background: Osteogenesis imperfecta (OI) is a heterogeneous group of inherited disorders characterised by susceptibility to fractures, primarily due to defects in type 1 collagen. The aim of this study is...
6.
Ozcan R, Hakalmaz A, Emre S, Karagoz A, Tutuncu C, Kurugoglu S, et al.
Pediatr Surg Int
. 2022 Sep;
38(11):1525-1531.
PMID: 36048241
Tubular esophageal duplication is a rare congenital malformation The surgical treatment of this lesion can be challenging. We aimed to present our experience in two cases with tubular esophageal duplication....
7.
Arslan E, Saygili S, Celkan T, Kurugoglu S, Elicevik M, Camcioglu A, et al.
Pediatr Nephrol
. 2022 Feb;
37(10):2415-2426.
PMID: 35118543
Background: There is evidence of increased risk of hypertension, albuminuria, and development of chronic kidney disease (CKD) in long-term follow-up of survivors of Wilms tumor (WT). However, most studies were...
8.
Gemicioglu B, Uzun H, Borekci S, Karaali R, Kurugoglu S, Atukeren P, et al.
J Infect Dev Ctries
. 2021 Nov;
15(10):1415-1425.
PMID: 34780364
Introduction: We aimed to evaluate clinical and laboratory findings of hospitalized asthma and chronic obstructive pulmonary disease (COPD) patients with COVID-19 and demonstrate that they have different symptoms and/or laboratory...
9.
Huseynov M, Ozcan R, Emre S, Canpolat N, Kurugoglu S, Sayman H, et al.
Turk J Med Sci
. 2021 Apr;
51(4):2029-2035.
PMID: 33896147
Background/aim: The criteria for surgical management of ureteropelvic junction obstruction are not well-defined, and there is a risk for loss of renal function before the operation. In this context, certain...
10.
Kalyoncu Ucar A, Kurugoglu S
Front Pediatr
. 2020 Oct;
8:546.
PMID: 33042907
Ultrasound is the main imaging study used to diagnose ureteropelvic junction (UPJ) obstruction. On ultrasound, abnormal dilatation of the pelvicalyceal system of varying degrees is seen, whereas the ureter is...