Ugur Demirsoy
Overview
Explore the profile of Ugur Demirsoy 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
25
Citations
100
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Dogan M, Demirsoy U, Basar E, Babaoglu K
J Pediatr Hematol Oncol
. 2023 Dec;
46(2):e205-e207.
PMID: 38113229
Mediastinal radiotherapy for childhood cancers, particularly Hodgkin disease, has numerous potential adverse effects, including coronary artery disease, pericarditis, cardiomyopathy, valvular disease, and conduction abnormalities. The prevalence of valvular stenosis is...
2.
Mese I, Altintas Mese C, Demirsoy U, Anik Y
Pediatr Radiol
. 2023 Dec;
54(1):1-11.
PMID: 38041712
In pediatric radiology, balancing diagnostic accuracy with reduced radiation exposure is paramount due to the heightened vulnerability of younger patients to radiation. Technological advancements in computed tomography (CT) reconstruction techniques,...
3.
Yaprak Bayrak B, Yildiz D, Demirsoy U, Corapcioglu F, Anik Y, French C
Asian Biomed (Res Rev News)
. 2023 Aug;
14(5):203-208.
PMID: 37551266
Background: Nuclear protein in testis (NUT) midline carcinoma (NMC) is an undifferentiated carcinoma, usually localized to the midline and presenting a translocation in the gene for bromodomain containing protein 4....
4.
Gallon R, Phelps R, Hayes C, Brugieres L, Guerrini-Rousseau L, Colas C, et al.
Gastroenterology
. 2022 Dec;
164(4):579-592.e8.
PMID: 36586540
Background & Aims: Constitutional mismatch repair deficiency (CMMRD) is a rare recessive childhood cancer predisposition syndrome caused by germline mismatch repair variants. Constitutional microsatellite instability (cMSI) is a CMMRD diagnostic...
5.
Kilci F, Demirsoy U, Jones J, Cakir O, Cizmecioglu-Jones F
J Pediatr Endocrinol Metab
. 2022 May;
35(8):1107-1112.
PMID: 35534911
Objectives: Ectopic parathyroid hormone (PTH) secretion is rare in children with rhabdomyosarcoma, and only a few pediatric cases have been reported to date. Reports of the use of zoledronic acid...
6.
Demirsoy U, Corapcioglu F
Eur J Med Genet
. 2021 Feb;
64(3):104167.
PMID: 33588069
There are few guidelines for genetic counseling and management of pediatric cancer patients with probable cancer predisposition. In this study, we used a previously proposed patient selection tool by Jongmans...
7.
Yildirimcakar D, Demirsoy U, Azizoglu M, Corapcioglu F
J Drugs Dermatol
. 2020 Dec;
19(12):1156-1165.
PMID: 33346523
Background: Infantile hemangiomas are the most common vascular tumors in childhood. Although spontaneous regression is common; several infantile hemangioma patients need treatment due to possible morbidities. The aim of this...
8.
Azizoglu M, Demirsoy U, Kulac I, Aktas S, Corapcioglu F
Fetal Pediatr Pathol
. 2020 Apr;
40(6):717-722.
PMID: 32242756
Although neuroblastoma and Ewing sarcoma/Primitive neuroectodermal tumor are different clinical entities, they are both a member of small round blue cell tumors and can mimic each other's behavior in clinical...
9.
Demirsoy U, Alparslan B, Sen M, Anik Y, Akansel G, Gorur G, et al.
Turk J Pediatr
. 2019 Sep;
61(1):139-141.
PMID: 31559737
Demirsoy U, Alparslan B, Şen MC, Anık Y, Akansel G, Görür G, Gürel B, Aksu G, Çorapçıoğlu F. More than Ophelia syndrome: Multiple paraneoplastic syndromes in pediatric Hodgkin lymphoma. Turk...
10.
Gonzalez-Acosta M, Marin F, Puliafito B, Bonifaci N, Fernandez A, Navarro M, et al.
J Med Genet
. 2019 Sep;
57(4):269-273.
PMID: 31494577
Introduction: Lynch syndrome (LS) and constitutional mismatch repair deficiency (CMMRD) are hereditary cancer syndromes associated with mismatch repair (MMR) deficiency. Tumours show microsatellite instability (MSI), also reported at low levels...