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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: szutkowski z. 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.
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
Schiavi F, Boedeker CC, Bausch B, Peçzkowska M, Gomez CF, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann MM, Berlis A, Brink I, Cybulla M, Muresan M, Walter MA, Forrer F, Välimäki M, Kawecki A, Szutkowski Z, Schipper J, Walz MK, Pigny P, Bauters C, Willet-Brozick JE, Baysal BE, Januszewicz A, Eng C, Opocher G, Neumann HP; European-American Paraganglioma Study Group. Schiavi F, et al. Among authors: szutkowski z. JAMA. 2005 Oct 26;294(16):2057-63. doi: 10.1001/jama.294.16.2057. JAMA. 2005. PMID: 16249420
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: szutkowski z. Neuroendocrinology. 2015;101(4):321-30. doi: 10.1159/000381458. Epub 2015 Mar 13. Neuroendocrinology. 2015. PMID: 25791839
21 results