Search Results - "PODA, Mehveş"

OKÜLT HEPATİT B VİRÜSÜNÜN GENOTİP, SUBGENOTİP VE SUBTİP ANALİZİ by Çakal, Bülent, Atasoy, Alp, Çavuş, Bilger, Çifcibaşı Örmeci, Aslı, Poda, Mehveş, Bulakçı, Mesut, Güllüoğlu, Mine, Günver, Mehmet, Akyüz, Filiz

“…Amaç: Okült Hepatit B Virus (HBV) enfeksiyonu (Occult HBV infection; OBI) mevcut serolojik testler ile HBV yüzey antijeni (Surface antigen; HBsAg) negatif…”
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What is the clinical impact of occult HBV infections and anti‐HBc positivity in patients with chronic hepatitis C? by Cakal, Bulent, Cavus, Bilger, Atasoy, Alp, Poda, Mehves, Bulakci, Mesut, Gulluoglu, Mine, Demirci, Mehmet, Sener, Leyla Turker, Altunok, Damla, Arslan, Asli Berru, Akyuz, Filiz

“…Occult hepatitis B infection (OBI) is defined by the persistence of the hepatitis B virus (HBV) genome in the liver of individuals testing negative for…”
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Prognostic Value of NTCP p.Ser267Phe Variant in Patients with Chronic Hepatitis B by ÇAKAL, Bülent, ATASOY, Alp, PODA, Mehveş, ÇAVUŞ, Bilger, BULAKÇI, Mesut, GÜLLÜOĞLU, Mine, AKYÜZ, Filiz

“…Aim: In this study, the aim is to detect polymorphisms in the gene encoding the sodium taurocholate cotransporting polypeptide (NTCP), the functional receptor…”
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Comparison of S gene mutations in patients with occult and chronic hepatitis B virus infection by Cakal, Bulent, Cavus, Bilger, Atasoy, Alp, Altunok, Damla, Poda, Mehves, Bulakci, Mesut, Gulluoglu, Mine, Demirci, Mehmet, Sener, Leyla Turker, Arslan, Aslı Berru, Arikan, Muzaffer, Akyuz, Filiz

“…This study aimed to detect mutations in the HBV S gene and evaluate their relationship to occult hepatitis B virus (HBV) infection (OBI). The study included 32…”
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Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey by Durmuş, Hacer, Matur, Zeliha, Atmaca, Murat Mert, Poda, Mehves, Çakar, Arman, Ulaş, Ümit Hıdır, Oflazer-Serdaroğlu, Piraye, Deymeer, Feza, Parman, Yesim G

“…Highlights • The clinical and genetic features of 17 patients from Turkey with TTR-FAP • Five different mutations (Val30Met, Glu89Gln, Gly53Glu, Glu54Gly,…”
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Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11 : evidence for further locus heterogeneity by CHRISTODOULOU, Kyproula, DEYMEER, Feza, SERDAROGLU, Piraye, ÖZDEMIR, Coskun, PODA, Mehves, GEORGIOU, Domna-Maria, IOANNOU, Panos, TSINGIS, Marios, ZAMBA, Eleni, MIDDLETON, Lefkos T

“…Friedreich's ataxia (FRDA), the most-common form of autosomal recessive ataxia, is inherited in most cases by a large expansion of a GAA triplet repeat in the…”
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Case report of fatal Mycobacterium tilburgii infection by Akpinar, Timur, Bakkaloglu, Oguz K, Ince, Burak, Tufan, Fatih, Kose, Murat, Poda, Mehves, Tascioglu, Didem, Koksalan, O. Kaya, Saka, Bulent, Erten, Nilgun, Buyukbabani, Nesimi, Kilicaslan, Zeki, Tascioglu, Cemil

“…Abstract There are few reports concerning Mycobacterium tilburgii infection in humans because this bacterium is non-cultivatable. Herein, using new molecular…”
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Pretreatment with Octreotide Modulates iNOS Gene Expression, Mimics Surgical Delay, and Improves Flap Survival by GÖZÜ, Aydin, PODA, Mehveş, TASKIN, Elif I, TURGUT, Hürriyet, ERGINEL-ÜNALTUNA, Nihan, DOGRUMAN, Hüsniye, ÖZSOY, Zafer

“…We aimed to evaluate the role of a synthetic somatostatin analogue in delay procedure of experimental skin flaps. Thirty-six rats were randomly divided into 2…”
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TÜRKİYE POPÜLASYONUNDA HLA-DQ POLİMORFİZMLERİNİN HEPATİT B VİRÜS ENFEKSİYONU İLE İLİŞKİSİ by Çakal, Bülent, Arıkan, Muzaffer, Atasoy, Alp, Çavuş, Bilger, Poda, Mehveş, Bulakçı, Mesut, Güllüoğlu, Mine, Demirci, Mehmet, Akyüz, Filiz

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CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome by Ozsait, Bilge, Kömürcü Bayrak, Evrim, Poda, Mehveş, Can, Günay, Hergenç, Gülay, Onat, Altan, Humphries, Steve E, Erginel Unaltuna, Nihan

“…In this study, our aim was to investigate the association of cholesterol ester transfer protein (CETP) TaqIB polymorphism with the likelihood of metabolic…”
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Natural history of SMA IIIb : Muscle strength decreases in a predictable sequence and magnitude by DEYMEER, Feza, SERDAROGLU, Piraye, PARMAN, Yesim, PODA, Mehves

“…To assess the natural progression of muscle weakness in spinal muscular atrophy (SMA) IIIb. Ten patients with SMA IIIb were followed for at least 10 years. Age…”
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Genotypic and Phenotypic Presentation of TTR- FAP in Turkey (P2.034) by Durmus, Hacer, Matur, Zeliha, Poda, Mehves, Atmaca, Mert Murat, Serdaroglu, Piraye, Deymeer, Feza, Parman, Yesim

“…Abstract only…”
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ANALYSIS OF GENOTYPE, SUBGENOTYPE AND SEROTYPE OF OCCULT HEPATITIS B VIRUS/OKULT HEPATIT B VIRUSUNUN GENOTIP, SUBGENOTIP VE SUBTIP ANALIZI by Cakal, Bulent, Atasoy, Alp, Cavus, Bilger, Ormeci, Asli, Poda, Mehves, Bulakci, Mesut, Gulluoglu, Mine, Gunver, Mehmet Guven, Akyuz, Filiz

“…Objective: Occult hepatitis B infection (OBI) can be characterized by the long-term persistence of HBV DNA in the liver of individuals who test negative for…”
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The effects of IL28B rs12979860 and rs8099917 polymorphism on Hepatitis B infection by Cakal, Bulent, Cavus, Bilger, Atasoy, Alp, Altunok, Damla, Poda, Mehves, Bulakci, Mesut, Gulluoglu, Mine, Demirci, Mehmet, Sener, Leyla Turker, Arslan, Asli Berru, Akyuz, Filiz

“…OBJECTIVE: The purpose of this study was to evaluate the relationship of IL28B rs12979860 and rs8099917 polymorphisms with the clinical, histological, and…”
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Genotypic and phenotypic presentation of Glu89Gln mutation in Turkey by Durmus, Hacer, Matur, Zeliha, Atmaca, Murat Mert, Poda, Mehves, Cakar, Arman, Serdaroglu-Oflazer, Piraye, Deymeer, Feza, Parman, Yesim

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Genotype-Phenotype Evaluation In 476 Turkish Dystrophinopathy Patients (P5.089) by Durmus, Hacer, Erginel-Unaltuna, Nihan, Mehves, Poda, Çakar, Arman, Altinkaya, Ayca, Guclu-Geyik, Filiz, Deymeer, Feza, Parman, Yesim, Tolun, Asli, Serdaroglu, Piraye

“…Abstract only…”
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Gender-modulated impact of apolipoprotein A5 gene (APOA5) -1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults by Komurcu-Bayrak, Evrim, Onat, Altan, Poda, Mehves, Humphries, Steve E, Palmen, Jutta, Guclu, Filiz, Can, Gunay, Erginel-Unaltuna, Nihan

“…Apolipoprotein A5 (APOA5) gene polymorphisms are usually associated with plasma triglyceride levels. We evaluated the relationship of the APOA5 -1131T>C and…”
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The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks by Komurcu-Bayrak, Evrim, Onat, Altan, Poda, Mehves, Humphries, Steve E., Acharya, Jayshree, Hergenc, Gülay, Coban, Neslihan, Can, Gunay, Erginel-Unaltuna, Nihan

“…We evaluated the relationship of the lipoprotein lipase (LPL) S447X variant with serum lipid levels and the metabolic syndrome (MS) in the Turkish Adult Risk…”
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Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time by Deymeer, Feza, Serdaroğlu, Pıraye, Poda, Mehveş, Gülşen-Parman, Yeşim, Özçelık, Tayfun, Özdemır, Coşkun

“…We examined 26 spinal muscular atrophy type III (SMA III) patients with SMNt deletions, searching for possible segmental distribution of muscle weakness. In…”
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Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time1This work was presented at the New Challenges in Neuromuscular Disorders, 25–27 September 1996, London, UK.1 by Deymeer, Feza, Serdaroğlu, Pıraye, Poda, Mehveş, Gülşen-Parman, Yeşim, Özçelık, Tayfun, Özdemır, Coşkun

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