Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Selma Düzenli"'
Publikováno v:
Journal of Urological Surgery, Vol 10, Iss 4, Pp 290-294 (2023)
Objective: To evaluate the relationship between sodium citrate cotransporter (NaDC-1) gene polymorphism and urinary citrate excretion in patients with kidney stones containing calcium. Materials and Methods: Between June 2009 and August 2011, stone m
Externí odkaz:
https://doaj.org/article/b89b58ec373b4121ba6283924435568b
Autor:
Natascia Tahani, Pietro Maffei, Hélène Dollfus, Richard Paisey, Diana Valverde, Gabriella Milan, Joan C. Han, Francesca Favaretto, Shyam C. Madathil, Charlotte Dawson, Matthew J. Armstrong, Adrian T. Warfield, Selma Düzenli, Clair A. Francomano, Meral Gunay-Aygun, Francesca Dassie, Vincent Marion, Marina Valenti, Kerry Leeson-Beevers, Ann Chivers, Richard Steeds, Timothy Barrett, Tarekegn Geberhiwot
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-22 (2020)
Abstract Alström Syndrome (ALMS) is an ultra-rare multisystem genetic disorder caused by autosomal recessive variants in the ALMS1 gene, which is located on chromosome 2p13. ALMS is a multisystem, progressive disease characterised by visual disturba
Externí odkaz:
https://doaj.org/article/f52e156af0f74a13905c04ea325feb2c
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 41, Iss 1, Pp 64-67 (2013)
Pacemaker (PM)-related thrombosis is an infrequent complication of pacing. We present the case of a 58-year-old man with heart failure and atrial fibrillation who had recurrent episodes of PM lead thrombosis while undergoing anticoagulation therapy.
Externí odkaz:
https://doaj.org/article/34638e689e124e7b82fd7030cea60fd4
Autor:
Ali Osman Arslan, Selma Düzenli
Publikováno v:
Sağlık Bilimleri Dergisi. 28:75-80
1. Amaç: Çalışmamızda, Sitokrom p450 enzimlerini kodlayan CYP ve vitamin K epoksit redüktaz kompleks subünit1 enzimini kodlayan VKORC1 genlerinin alt gruplarındaki tek nükleotit polimorfizmlerinin muhtemel bireysel ve ortak etkilerini prosta
Autor:
Arzu Guler Karakuz, Cansu Kara Oztabag, Selma Düzenli, Mehmet Ata Topcuoglu, Mustafa Ayhan Ekici
Publikováno v:
EXPERIMENTAL BIOMEDICAL RESEARCH; Vol 2 No 1 (2019): Experimental Biomedical Research; 29-36
Aim: Polycystic ovary syndrome (PCOS) is a multifactorial, endocrine, and metabolic disorder seen in 10%-20% of women of reproductive age. Due to the close relationshipobserved between the increased risk of type 2 diabetes and insulin resistance and
Autor:
Shyam Madathil, Hélène Dollfus, Vincent Marion, Timothy Barrett, Ann Chivers, Marina Valenti, Richard P. Steeds, Clair A. Francomano, Natascia Tahani, Matthew J. Armstrong, Meral Gunay-Aygun, Charlotte Dawson, Selma Düzenli, Pietro Maffei, Gabriella Milan, Kerry Leeson-Beevers, Francesca Favaretto, Tarekegn Geberhiwot, Joan C. Han, Adrian T. Warfield, Francesca Dassie, Diana Valverde, Richard B Paisey
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-22 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-22 (2020)
Alström Syndrome (ALMS) is an ultra-rare multisystem genetic disorder caused by autosomal recessive variants in the ALMS1 gene, which is located on chromosome 2p13. ALMS is a multisystem, progressive disease characterised by visual disturbance, hear
Autor:
Yusuf Velioğlu, Kemalettin Erdem, Selma Düzenli, Ufuk Turan Kursat Korkmaz, Erhan Renan Uçaroğlu, Bahadır Dağlar, Ayhan Cetinkaya, Ali Osman Arslan, Ahmet Yuksel
Objectives: To evaluate patients diagnosed with venous thromboembolism (VTE) in terms of hereditary thrombophilic risk factors and to assess genetic and biochemical factors affecting the development of VTE. Methods: Sixty patients with VTE and 23 con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b743c19ee897ab57f2423fb1642e0e1
https://app.trdizin.gov.tr/makale/TXpjeU16QXdNQT09
https://app.trdizin.gov.tr/makale/TXpjeU16QXdNQT09
Autor:
Ozlem Kucukhuseyin, Ali Osman Arslan, Bulent Duran, Şakir Zeybek, Selma Düzenli, Faruk Çelik, Ilhan Yaylim, Murat Diramali
Publikováno v:
EXPERIMENTAL BIOMEDICAL RESEARCH; Vol 2 No 1 (2019): Experimental Biomedical Research; 8-19
Aim: To investigate the possible effects of polymorphisms in genes encoding some important antioxidant enzymes such as super oxide dismutase 2 (SOD2), glutathione peroxidase 1 (GPX1), endothelial NOS (eNOS) and catalase (CAT) in patients with polycys
Autor:
Tolga Karakan, Ali Osman Arslan, Ali Akkoc, Serkan Ozcan, Selma Düzenli, Omer Faruk Yagli, Ahmet Metin
Publikováno v:
EXPERIMENTAL BIOMEDICAL RESEARCH; Vol 1 No 4 (2018): Experimental Biomedical Research; 128-134
Aim: The causes of prostate cancer development and molecular mechanism underlying its development and progression are not clearly understood. The aim of this study is to determine the frequency of G1733A (rs6152) polymorphism of the androgen receptor
Autor:
Taner Yavuz, Omer Polat, Sevil Altunrende, Erkan Yesiller, Selma Düzenli, Ali Kiliçgün, Melih Güven, Halil Ibrahim Atasoy
Publikováno v:
European Journal of Pediatrics. 172:269-272
Poland syndrome has been reported to be associated with true dextrocardia, but not with true situs inversus. In this report, we describe the first patient with total situs inversus in medical literature and try to highlight the syndrome's probable et