Výsledky vyhledávání - "Feryal Cabuk"

Association of MTHFR A1298C polymorphism with conotruncal heart disease

Autor: Feryal Cabuk, Cihat Sanli, Murat Koç, Beyza D. Sayin Kocakap, Ali Kutsal

Koc, Murat/0000-0003-4555-2151 WOS: 000361384800015 PubMed: 25547204 Congenital heart diseases are common congenital anomalies with 1% prevalence worldwide and are associated with significant childhood morbidity and mortality. Among a wide range of a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d39e702646f15dc660f78eefce6c7225
https://hdl.handle.net/20.500.12587/6050

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Tolmetin and salicylate therapy in acute rheumatic fever: Comparison of clinical efficacy and side-effects

Autor: Selmin Karademir, Filiz Şenocak, Feryal Cabuk, Cemşit Karakurt, Burhan Öcal, Deniz Oğuz

Publikováno v: Pediatrics International. 45:676-679

Background: The arthritis of rheumatic fever is very responsive to treatment with salicylates, but there are many adverse reactions, especially hepatotoxicity, due to aspirin (acetylsalicylic acid) therapy. These side-effects change the course and du

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78478b8a4667b924c5d217438a3b263b
https://doi.org/10.1111/j.1442-200x.2003.01801.x

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Myocardial Performance Index Combining Systolic and Diastolic Myocardial Performance in Doxorubicin-Treated Patients and Its Correlation to Conventional Echo/Doppler Indices

Autor: Burhan Öcal, Dilek Birgen, Nazmiye Yüksek, Ulya Ertem, Selmin Karademir, Deniz Oğuz, Feryal Cabuk

Publikováno v: Pediatric Cardiology. 23:522-527

This study was designed to evaluate the utility of myocardial performance index (MPI) in anthracycline cardiotoxicity. The MPI measures the ratio of total time spent in isovolumic activity (isovolumetric contraction time and isovolumetric relaxation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd4c98dec2898aebf00b34fe9eeeb09e
https://doi.org/10.1007/pl00021001

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The prevalence of mental retardation by gender, age of diagnosis and location in Zonguldak province, Turkey

Autor: Ferruh N, Ayoglu, Feryal, Cabuk, Sibel, Kiran, Ayse, Ocakci, Zuhtu, Sahin, Ahmet, Dursun

Publikováno v: Neurosciences (Riyadh, Saudi Arabia). 13(1)

To evaluate the prevalence of mental retardation by gender, age of diagnosis, and location in Zonguldak, Turkey.The data of 1909 mentally retarded children recorded between 1995 and 2003 was obtained from the Learning Disability Guidance and Research

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9832a399cf96e8a2d0b2964e16a2a654
https://pubmed.ncbi.nlm.nih.gov/21063288

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Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction

Autor: Dagan Jenkins, Zoran Gucev, Xavier Caubit, Laurent Fasano, Nadica Matevska, Claire M. Lye, Feryal Cabuk, Aleksandar Dimovski, Adrian S. Woolf, Velibor Tasic

Publikováno v: Nephrology Dialysis Transplantation
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2010, 25 (1), pp.54-60. ⟨10.1093/ndt/gfp453⟩
Nephrology Dialysis Transplantation, 2010, 25 (1), pp.54-60. ⟨10.1093/ndt/gfp453⟩

Background. Congenital pelvi-ureteric junction obstruction (PUJO) affects 0.3% of human births. It may result from aberrant smooth muscle development in the renal pelvis, resulting in hydronephrosis. Mice that are null mutant for the Teashirt3 (Tshz3

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6445d3ef4a477eb9888b8dfcb1224582
https://pubmed.ncbi.nlm.nih.gov/19745106

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Relationship of apoE polymorphism with lipoprotein(a), apoA, apoB and lipid levels in atherosclerotic infarct

Autor: Savas Baris, Esra Aciman, Ahmet Dursun, Görkem Mungan, Handan Ankarali, Vildan Sumbuloglu, Sureyya Ekem, Feryal Cabuk, Nida Tascilar, Sevcan Tug Bozdogan

Publikováno v: Journal of the neurological sciences. 277(1-2)

Background and purpose: Apolipoprotein E (apoE) polymorphism is suggested to be a risk factor in stroke in some populations, either by affecting lipid parameters or independently. Its effect on lipoprotein(a) [Lp(a)] is not known. The roles of apoE p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b8650fdccba1bfb7cc5c4686d3468c8
https://pubmed.ncbi.nlm.nih.gov/18945448

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TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy

Autor: Feryal, Cabuk, Halil G, Karabulut, Timur, Tuncali, Selmin, Karademir, Mithat, Bozdayi, Ajlan, Tükün

Publikováno v: The Turkish journal of pediatrics. 49(1)

Fallot tetralogy (FT) is the most frequently observed conotruncal heart defect (CTHD) and accompanies 15% of the 22q11 deletion syndromes, DiGeorge/ velocardiofacial (DGS/VCFS) syndromes. TBX1 is a gene located in the 22q11 region and has a role in n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b223077701da8a3e98c5fd61ecf247e
https://pubmed.ncbi.nlm.nih.gov/17479646

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