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Burcu Albuz
Observed names:
ALBUZ, BURCU,
Albuz, Burcu,
Burcu ALBUZ
Institution:
Denizli Devlet Hastanesi
Observed institutions:
Çanakkale Onsekiz Mart Üniversitesi,
University Ferhat Abbas of Setif,
Sağlık Bilimleri Üniversitesi,
Denizli Devlet Hastanesi,
Pamukkale Üniversitesi Hastaneleri,
Pamukkale University
show all 6
ORCID:
0000-0002-9874-0781
Observed ORCID:
0000-0002-9874-0781
OpenAlex ID:
A5013932981
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy
2018
·
Anna Fassio
, Alessandro Esposito
, et al.
·
Brain
·
89
PDF
Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings
2017
·
Bayram Özhan
, Özlem Boz Anlaş
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
11
PDF
A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type
2019
·
Burcu Albuz
, Gökhan Ozan Çetin
, et al.
·
Clinical Dysmorphology
·
9
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients
2021
·
Burcu Albuz
, Ozturk Ozdemir
, et al.
·
Clinical Neurology and Neurosurgery
·
6
Blau syndrome with a rare mutation in exon 9 of NOD2 gene
2019
·
Jelena Velickovic
, Fatma Silan
, et al.
·
Autoimmunity
·
5
Is Prescription Drug Abuse in Prisons Changing? A Preliminary Study with Prison Doctors -
2015
·
Ceyhan Balcı Şengül
, Cem Şengül
, et al.
·
Journal of Dependence
·
3
Analysis of Differences in DNA Damage and Repair Efficacy in Lymphocytes of Patients with Bipolar Disorder
2022
·
Mehmet Mart
, Gökçe Mart
, et al.
·
Turkish Journal of Psychiatry
·
2
A rare missense Duchenne muscular dystrophy gene variant in a family with muscular dystrophy from Turkey
2022
·
Onur Tokgün
, Burcu Albuz
, et al.
·
The European Research Journal
·
1
PDF
Mikrodelesyon ve Mikroduplikasyon Sendromları
2018
·
Cavidan Nur Semerci Gündüz
, Burcu Albuz
·
Turkiye Klinikleri Medical Genetics - Special Topics
·
1
Next‐Generation Sequencing in Pediatric Lipid Disorders: Expanding the Genetic Landscape and Clinical Understanding
2026
·
Ozlem Boz
, Burcu Albuz
, et al.
·
Pediatrics International
PDF
The effects of working conditions on work life in Familial Mediterranean Fever (FMF) patients
2023
·
Savaş KANBUR
, Burcu ALBUZ
, et al.
·
DAHUDER Medical Journal
PDF
Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID ‐19 pandemic
2022
·
Mehmet Berkay Akcan
, Burcu Albuz
, et al.
·
International Journal of Rheumatic Diseases
The evaluation of FMF course and colchicine treatment in the patients with or without COVID-19 symptoms during the pandemic
2021
·
Özdemir, Öztürk
, Sılan, Fatma
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Çanakkale İlimizdeki Jinekolojik Kanserlerde Yeni Nesil DNA Dizi Analizi ile Saptanan Mutasyon Profilleri
2020
·
ŞAHİN, HACI ÖZTÜRK
, SILAN, FATMA
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Jinekolojik Kanserlerde Yeni Nesil DNA Dizi Analizi ile Saptanan Mutasyon Profilleri: Tek Merkez Vaka Serisi Sonuçlarımız
2020
·
H.öztürk ŞAHİN
, Kübra ÖZKAN
, et al.
·
Uludağ Üniversitesi Tıp Fakültesi Dergisi
PDF
A novel variant for SQSTM1 gene in a patient with frontotemporal dementia.
2020
·
ÖZDEMİR, ÖZTÜRK
, SILAN, FATMA
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report
2020
·
Fatma SILAN
, Burcu ALBUZ
, et al.
·
Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi
PDF
A Rare Chromosomal Aneuploidy That Diagnosed With Array CGH And MLPA Validation : Trisomy 4 in a fetus
2020
·
SÖNMEZ, VOLKAN
, ÖZDEMİR, ÖZTÜRK
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Homozygous Frameshi̇ft Mutati̇on İn Ddb2 Gene İnduced Squamous Cell and Basal Cell Carci̇nomas İn a Chi̇ld Wi̇th Xeroderma Pi̇gmentosum
2020
·
ÖZDEMİR, ÖZTÜRK
, SILAN, FATMA
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Epilepsi hastalarında kromozomal kopya sayısı değişikliklerinin (CNV) aCGH yöntemi ile retrospektif olarak araştırılması
2019
·
Burcu Albuz
·
Çanakkale Onsekiz Mart University AVESIS
BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q
2019
·
ÖZTÜRK, MENEKŞE
, ALBUZ, BURCU
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
A rare heterochromatin polymorphism of chromosome 6 associated with recurrent miscarriage: A case report
2019
·
ÖZTÜRK, MENEKŞE
, ALBUZ, BURCU
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Otoinflamatuar Hastalıklar ve Genetik
2019
·
Menekşe Öztürk
, Burcu Albuz
, et al.
·
Turkiye Klinikleri Medical Genetics - Special Topics
Türkiye Klinikleri Tıbbi Genetik - Özel Konular Genetik ve Multidisipliner Yaklaşımlar
2019
·
ALBUZ, BURCU
, ÖZTÜRK, MENEKŞE
, et al.
·
Çanakkale Onsekiz Mart University AVESIS
Türkiye Klinikleri Tıbbi Genetik - Özel Konular-Sitogenetik
2018
·
SEMERCİ GÜNDÜZ, CAVİDAN NUR
, ALBUZ, BURCU
·
AYBU AVESIS
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Works count:
30
Citation count:
127
H-index:
5
I10-index:
2
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