Elcin Bora
Overview
Explore the profile of Elcin Bora including associated specialties, affiliations and a list of published articles.
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Articles
29
Citations
73
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0
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Recent Articles
1.
Aslan P, Caglayan A, Bora E, Koc A, Yucel H, Ulgenalp A, et al.
Turk J Gastroenterol
. 2024 Aug;
35(5):374-384.
PMID: 39115133
Peutz-Jeghers syndrome (PJS) is a rare hereditary disorder linked to increased cancer risk due to specific genetic variants in the STK11 gene. This study aimed to assess disease manifestations, genetic...
2.
Ozkalayci H, Bora E, Cankaya T, Kocabey M, Zubari N, Yis U, et al.
Neurogenetics
. 2024 Jun;
25(3):201-213.
PMID: 38850354
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive allelic muscle diseases caused by dystrophin gene mutations. Eight hundred thirty-seven patients admitted between 1997 and 2022 were...
3.
Bora E, Bulut A, Cankaya T, Cinleti T, Genc H, Ozcan E, et al.
Mol Syndromol
. 2023 Oct;
14(5):363-374.
PMID: 37901857
Introduction: Long QT syndrome (LQTS) is a disorder of ventricular myocardial repolarization characterized by a prolonged QT interval on the electrocardiogram. It increases the risk of ventricular arrhythmias, which can...
4.
Demir S, Cagliyan E, Ozturk D, Ozmen S, Altunyurt S, Cankaya T, et al.
J Obstet Gynaecol
. 2022 Aug;
42(7):2899-2904.
PMID: 36006022
The aim of this study is to retrospectively examine invasive diagnostic methods, structural anomalies accompanying cystic hygroma, and pregnancy outcomes in cystic hygroma cases admitted to a tertiary centre. The...
5.
Bora E, Caglayan A, Koc A, Cankaya T, Ozkalayci H, Kocabey M, et al.
Cancer Genet
. 2022 Feb;
262-263:118-133.
PMID: 35220195
Breast cancer, a worldwide leading cause of cancer in women, may occur in familial cases. Germline mutations in BRCA1/2 genes are responsible for 15% of the familial cases. With the...
6.
Dundar M, Fahrioglu U, Yildiz S, Bakir-Gungor B, Temel S, Akin H, et al.
Funct Integr Genomics
. 2022 Jan;
22(3):291-315.
PMID: 35098403
Familial Mediterranean fever (FMF) is a monogenic autoinflammatory disorder with recurrent fever, abdominal pain, serositis, articular manifestations, erysipelas-like erythema, and renal complications as its main features. Caused by the mutations...
7.
Akdal G, Kocoglu K, Bora E, Koc A, Ulgenalp A, Bedir M, et al.
Neurol Clin Pract
. 2021 Apr;
11(2):e129-e134.
PMID: 33842081
Purpose Of Review: To report the findings in 12 members over 3 generations of a family with dominantly inherited Charcot-Marie-Tooth disease (CMT1B) due to a novel mutation, who all had...
8.
Vural A, Simsir G, Tekgul S, Kocoglu C, Akcimen F, Kartal E, et al.
Mov Disord
. 2021 Feb;
36(7):1676-1688.
PMID: 33624863
Background: The genetic and epidemiological features of hereditary ataxias have been reported in several populations; however, Turkey is still unexplored. Due to high consanguinity, recessive ataxias are more common in...
9.
Akdal G, Kocoglu K, Kocoglu C, Bora E, Basak A, Halmagyi G
Clin Neurophysiol
. 2020 Nov;
132(1):77-79.
PMID: 33248435
No abstract available.
10.
Akdal G, Kocoglu K, Tanriverdizade T, Bora E, Bademkiran F, Yuceyar A, et al.
J Neurol
. 2020 Aug;
268(2):526-531.
PMID: 32862243
Objective: To find out if Charcot-Marie-Tooth (CMT) patients, who have peripheral vestibular as well as peripheral somatosensory impairment, have worse postural balance than those who do not. Methods: We studied...