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151 results
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Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.
Peczkowska M, Erlic Z, Hoffmann MM, Furmanek M, Cwikla J, Kubaszek A, Prejbisz A, Szutkowski Z, Kawecki A, Chojnowski K, Lewczuk A, Litwin M, Szyfter W, Walter MA, Sullivan M, Eng C, Januszewicz A, Neumann HP. Peczkowska M, et al. Among authors: prejbisz a. J Clin Endocrinol Metab. 2008 Dec;93(12):4818-25. doi: 10.1210/jc.2008-1290. Epub 2008 Sep 30. J Clin Endocrinol Metab. 2008. PMID: 18826997 Free PMC article.
Mortality associated with phaeochromocytoma.
Prejbisz A, Lenders JW, Eisenhofer G, Januszewicz A. Prejbisz A, et al. Horm Metab Res. 2013 Feb;45(2):154-8. doi: 10.1055/s-0032-1331217. Epub 2013 Jan 15. Horm Metab Res. 2013. PMID: 23322516 Review.
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
Pęczkowska M, Kowalska A, Sygut J, Waligórski D, Malinoc A, Janaszek-Sitkowska H, Prejbisz A, Januszewicz A, Neumann HP. Pęczkowska M, et al. Among authors: prejbisz a. Clin Endocrinol (Oxf). 2013 Dec;79(6):817-23. doi: 10.1111/cen.12218. Epub 2013 May 3. Clin Endocrinol (Oxf). 2013. PMID: 23551045
Measurements of plasma metanephrines by immunoassay vs liquid chromatography with tandem mass spectrometry for diagnosis of pheochromocytoma.
Weismann D, Peitzsch M, Raida A, Prejbisz A, Gosk M, Riester A, Willenberg HS, Klemm R, Manz G, Deutschbein T, Kroiss M, Därr R, Bidlingmaier M, Januszewicz A, Eisenhofer G, Fassnacht M. Weismann D, et al. Among authors: prejbisz a. Eur J Endocrinol. 2015 Mar;172(3):251-60. doi: 10.1530/EJE-14-0730. Epub 2014 Dec 1. Eur J Endocrinol. 2015. PMID: 25452465
Cardiovascular Risk in Primary Hyperaldosteronism.
Prejbisz A, Warchoł-Celińska E, Lenders JW, Januszewicz A. Prejbisz A, et al. Horm Metab Res. 2015 Dec;47(13):973-80. doi: 10.1055/s-0035-1565124. Epub 2015 Nov 17. Horm Metab Res. 2015. PMID: 26575306 Review.
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