Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cengiz Bölükbaş"'
Publikováno v:
İstanbul Medical Journal, Vol 21, Iss 4, Pp 327-329 (2020)
Kounis syndrome (KS) is an acute coronary syndrome secondary to allergic reactions and can be triggered by many factors. It is a rare condition that is difficult to diagnose, which delays the prognosis of the disease. KS can be classified into three
Externí odkaz:
https://doaj.org/article/d4276e3cd5f8409fb95b1a210cacc103
Autor:
Necati, Ormeci, Füsun, Bölükbaş, Esra, Erden, Sahin, Coban, Fuat, Ekiz, Hakan, Erdem, Murat, Palabıyıkoğlu, Ali Reşit, Beyler, Ismail, Balık, Cengiz, Bölükbaş, Yaşar, Nazlıgül, Seyfettin, Köklü
Publikováno v:
Hepato-gastroenterology. 58(110-111)
The aim of this study was to evaluate the efficacy of pegylated interferon (PEG-IFN) alfa-2b for short (one year) and long (two years) terms of treatment for chronic hepatitis D.Eighteen patients with chronic hepatitis D were administered PEG-IFN alf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bbcfd5259c71c519754af0f273ad428
https://pubmed.ncbi.nlm.nih.gov/22086695
https://pubmed.ncbi.nlm.nih.gov/22086695
Autor:
Cengiz, Bölükbaş, Füsun F, Bölükbaş, Oya, Ovünç, Güray, Kiliç, Remzi, Dalay, Hatice, Güven, Fikriye, Uras, Turay K, Yardimci, Mehmet H, Sökmen, Ahmet F, Agan, Nezih, Pişkinpaşa
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 17(3)
Serum pepsinogen levels are considered as a non-endoscopic blood test in the diagnosis of atrophic gastritis. The objective of the present study was to investigate whether there is any difference between pepsinogen levels in Helicobacter pylori-posit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23b18b82ef273217ece919258df59f3f
https://pubmed.ncbi.nlm.nih.gov/16941249
https://pubmed.ncbi.nlm.nih.gov/16941249
Autor:
Evren, Abut, Hakan, Güveli, Tülin, Kendir, Cengiz, Bölükbaş, Ali Tüzün, Ince, Ali Remzi, Dalay, Oya Ovünç, Kurdaş
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 15(2)
This report describes a case of Budd-Chiari syndrome caused by latent polycythemia vera and factor V Leiden mutation. This syndrome usually occurs due to thrombosis of hepatic veins or membranous obstruction of inferior vena cava. The most common rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::792bd28f482978393493ece5110212e5
https://pubmed.ncbi.nlm.nih.gov/15334320
https://pubmed.ncbi.nlm.nih.gov/15334320
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 14(2)
The case of a 65 year old woman referred for further evaluation of back pain and with abnormalities at ultrasound including increase in portal vein diameter and splenomegaly is presented. Other tests, including bone marrow biopsy and Doppler ultrasou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8646979fc1efceb39026532adcd06122
https://pubmed.ncbi.nlm.nih.gov/14614643
https://pubmed.ncbi.nlm.nih.gov/14614643
Autor:
Evren, Abut, Alper, Arman, Hakan, Güveli, Cengiz, Bölükbaş, Tülin, Kendir, Remzi, Dalay, Oya, Ovünç
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 14(2)
Situs ambiguous anomaly is a rarely encountered condition in clinical practice that is characterized by the presence of multiple congenital anomalies relevant to intraabdominal organs and the cardiovascular system. While this syndrome is mostly diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6189c7f03370d867a341fefbb5d33c3b
https://pubmed.ncbi.nlm.nih.gov/14614646
https://pubmed.ncbi.nlm.nih.gov/14614646
Autor:
Haci Mehmet, Sökmen, Ali Tüzün, Ince, Cengiz, Bölükbaş, Güray, Kiliç, Remzi, Dalay, Oya Ovünç, Kurdaş
Publikováno v:
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. 14(1)
Peutz-Jeghers syndrome is an autosomal dominantly inherited rare syndrome characterized by mucocutaneous pigmentations, with intestinal and extraintestinal polyps. It is accepted to be a precancerous syndrome. The polyps can cause anemia and intestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f49825fb9d3b596c8188bf7f089c277c
https://pubmed.ncbi.nlm.nih.gov/14593545
https://pubmed.ncbi.nlm.nih.gov/14593545
Publikováno v:
Gastroenterology. 114:A1318-A1319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef1b0c34e2105c83965455d224dae259
https://doi.org/10.1016/s0016-5085(98)85351-1
https://doi.org/10.1016/s0016-5085(98)85351-1