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14篇 您的检索式:作者名="Patocs"
    题名 作者 年代 出处 被引量
1Inflammation and oxidative stress caused might lead to left ventricular diastolic and hypertension by nitric oxide synthase uncoupling systolic dysfunction in patients with显示文摘Zsuzsanna Szelenyi Adam Fazakas Gabor Szenasi Melinda KiSS Narcis Tegze Bertalan CsabaFekete Eszter Nagy Imre Bodo Balint Nagy Attila Molvarec Attila Patocs Lilla Pepo Zoltan Prohatszka Andras Vereckei 2015Journal of Geriatric Cardiology2015,12,1:2
2Fast high-voltage resistive pulse divider显示文摘Racz B Patocs A 0,,03:1
3Novel mutation of the CYP17 gene in two unrelated patients with combined 17 alpha-hydroxylase/17,20 -lyase deficiency : Demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling 显示文摘Patocs A Liko I Varga I 2005J Steroid Biochem Mol Biol2005,97,3:1
4Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma显示文摘Kevin M Zbuk Attila Patocs Amy Shealy 0,,10:1
5A novel mechanism between typeⅡdiabetes mellitus and procalcitonin gene expression显示文摘Patocs A Liko I Varga I 2005FEBS Journal2005,272,1:1
6Breast-cancer stromal cells with TP53 mutations and nodal metastases 显示文摘Patocs A Zhang L Xu Y 2007N Engl J Med2007,357,25:1
7Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1显示文摘Balogh K Patocs A Majnik J 2004Mol Genet Metab2004,83,12:1
8Breast-cancer stromal cells with TP53 mutations and nodal metastases显示文摘Patocs A Zhang L Xu Y 2007N Engl J Med2007,357,:1
9Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy显示文摘Boyle B Koranyi K Patocs A 2008British Journal of Ophthalmology2008,92,1:1
10Overrepresentation of BclIpolyrnorphism of the glucocorticoid receptor gene in preg- nant women with HELLP syndrome显示文摘Bertalan R Patocs A Nagy B 2009Clinica Chimiea Acta2009,405,12:1
11Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1 显示文摘Balogh K Patocs A Majnik J 2008Mol Genet Metab2008,83,122:1
12VHL gene mutations in Hungar- ian families with yon Hippel - Lindau disease and patients with ap- parently sporadic unilateral pheochromocytomas 显示文摘Gergics P Patocs A Toth M 2009Eur J Endo- crino12009,161,:1
13Menin and itsinteracting proteins ; elucidation of menin function 显示文摘Balogh K Racz K Patocs A 2006Trends Endocrinol Metab2006,17,9:1
14Association between birthweight in preterm neonates and the BclI polymorphism of theglucocorticoid receptor gene显示文摘Bertalan R Patocs A Vasarhelyi B 2008J Steroid Biochem Mol Biol2008,111,12:1
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