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GROWTH RATE OF PARAGANGLIOMAS RELATED TO GERMLINE MUTATIONS OF THE SDHX GENES.
Michałowska I, Ćwikła JB, Michalski W, Wyrwicz LS, Prejbisz A, Szperl M, Nieć D, Neumann HP, Januszewicz A, Pęczkowska M. Michałowska I, et al. Among authors: neumann hp. Endocr Pract. 2017 Mar;23(3):342-352. doi: 10.4158/EP161377.OR. Epub 2016 Dec 14. Endocr Pract. 2017. PMID: 27967220
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: neumann hp. 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.
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: neumann hp. Clin Endocrinol (Oxf). 2013 Dec;79(6):817-23. doi: 10.1111/cen.12218. Epub 2013 May 3. Clin Endocrinol (Oxf). 2013. PMID: 23551045
Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography.
Michałowska I, Ćwikła JB, Pęczkowska M, Furmanek MI, Buscombe JR, Michalski W, Prejbisz A, Szperl M, Malinoc A, Moczulski D, Szutkowski Z, Kawecki A, Antoniewicz J, Pęczkowski P, Lewczuk A, Otto M, Cichocki A, Bednarek-Tupikowska G, Kabat M, Janaszek-Sitkowska H, Przybyłowska K, Janas J, Neumann HP, Januszewicz A. Michałowska I, et al. Among authors: neumann hp. Neuroendocrinology. 2015;101(4):321-30. doi: 10.1159/000381458. Epub 2015 Mar 13. Neuroendocrinology. 2015. PMID: 25791839
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
Erlic Z, Rybicki L, Peczkowska M, Golcher H, Kann PH, Brauckhoff M, Müssig K, Muresan M, Schäffler A, Reisch N, Schott M, Fassnacht M, Opocher G, Klose S, Fottner C, Forrer F, Plöckinger U, Petersenn S, Zabolotny D, Kollukch O, Yaremchuk S, Januszewicz A, Walz MK, Eng C, Neumann HP; European-American Pheochromocytoma Study Group. Erlic Z, et al. Among authors: neumann hp. Clin Cancer Res. 2009 Oct 15;15(20):6378-85. doi: 10.1158/1078-0432.CCR-09-1237. Epub 2009 Oct 13. Clin Cancer Res. 2009. PMID: 19825962
Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions.
Därr R, Pamporaki C, Peitzsch M, Miehle K, Prejbisz A, Peczkowska M, Weismann D, Beuschlein F, Sinnott R, Bornstein SR, Neumann HP, Januszewicz A, Lenders J, Eisenhofer G. Därr R, et al. Among authors: neumann hp. Clin Endocrinol (Oxf). 2014 Apr;80(4):478-86. doi: 10.1111/cen.12327. Epub 2013 Oct 17. Clin Endocrinol (Oxf). 2014. PMID: 24102244 Clinical Trial.
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
Erlic Z, Hoffmann MM, Sullivan M, Franke G, Peczkowska M, Harsch I, Schott M, Gabbert HE, Valimäki M, Preuss SF, Hasse-Lazar K, Waligorski D, Robledo M, Januszewicz A, Eng C, Neumann HP. Erlic Z, et al. Among authors: neumann hp. J Clin Endocrinol Metab. 2010 Jan;95(1):308-13. doi: 10.1210/jc.2009-1728. Epub 2009 Nov 11. J Clin Endocrinol Metab. 2010. PMID: 19906784 Free PMC article.
289 results