dc.contributor.author | KÖMÜR, SÜHEYLA | |
dc.contributor.author | Karasahin, Omer | |
dc.contributor.author | Kalkan, Irem Akdemir | |
dc.contributor.author | Dal, Tuba | |
dc.contributor.author | ALTUNIŞIK TOPLU, SİBEL | |
dc.contributor.author | Harputoglu, Murat | |
dc.contributor.author | Sarigul, Figen | |
dc.contributor.author | Mete, Ayse Ozlem | |
dc.contributor.author | Yildiz, Yesim | |
dc.contributor.author | Esmer, Fatih | |
dc.contributor.author | Kandemir, Ozlem | |
dc.contributor.author | NAZİK, SELÇUK | |
dc.contributor.author | İNAN, DİLARA | |
dc.contributor.author | Akgul, Fethiye | |
dc.contributor.author | Kaya, Safak | |
dc.contributor.author | Tunc, Nurettin | |
dc.contributor.author | BALIN, ŞAFAK ÖZER | |
dc.contributor.author | BAYINDIR, YAŞAR | |
dc.contributor.author | TAŞOVA, YEŞİM | |
dc.contributor.author | Akar, Fesih | |
dc.contributor.author | Oren, Meryem Merve | |
dc.contributor.author | Ayhan, Merve | |
dc.contributor.author | Demir, Yakup | |
dc.contributor.author | ÇELEN, MUSTAFA KEMAL | |
dc.date.accessioned | 2021-12-10T11:01:26Z | |
dc.date.available | 2021-12-10T11:01:26Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Karasahin O., Kalkan I. A. , Dal T., ALTUNIŞIK TOPLU S., Harputoglu M., Mete A. O. , KÖMÜR S., Sarigul F., Yildiz Y., Esmer F., et al., "Real-life Data for Tenofovir Alafenamide Fumarate Treatment of Hepatitis B: the Pythagoras Cohort", HEPATITIS MONTHLY, cilt.21, sa.2, 2021 | |
dc.identifier.issn | 1735-143X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_62f1a5f3-bd35-4572-9ff8-ecb9a0b8d2bd | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/171064 | |
dc.identifier.uri | https://doi.org/10.5812/hepatmon.104943 | |
dc.description.abstract | Background: Chronic hepatitis B (CHB) is a viral infection that can result in life-threatening conditions, such as hepatocellular carcinoma and cirrhosis. Tenofovir, which is used for the treatment of CHB, is a nucleotide analog that inhibits HBV-DNApolymerase and has two formulations: disoproxil and alafenamide. In contrast to tenofovir disoproxil fumarate (TDF), tenofovir alafenamide fumarate (TAF) penetrates the whole hepatocyte without being eliminated due to its longer plasma half-life and greater plasma stability. As a result, side effects such as proximal renal tubulopathy and loss of bone density are less common in the treatment of TAF and have similar efficacy to TDF. | |
dc.language.iso | eng | |
dc.subject | İç Hastalıkları | |
dc.subject | GASTROENTEROLOJİ VE HEPATOLOJİ | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Gastroenteroloji-(Hepatoloji) | |
dc.subject | Gastroenterology | |
dc.subject | Hepatology | |
dc.subject | Health Sciences | |
dc.title | Real-life Data for Tenofovir Alafenamide Fumarate Treatment of Hepatitis B: the Pythagoras Cohort | |
dc.type | Makale | |
dc.relation.journal | HEPATITIS MONTHLY | |
dc.contributor.department | Erzurum Bolge Training & Research Hospital , , | |
dc.identifier.volume | 21 | |
dc.identifier.issue | 2 | |
dc.contributor.firstauthorID | 2615839 | |