Erlic Z - Search Results

1

Autosomal dominant polycystic kidney disease: prevalence of renal neoplasias in surgical kidney specimens.

Jilg CA, Drendel V, Bacher J, Pisarski P, Neeff H, Drognitz O, Schwardt M, Gläsker S, Malinoc A, Erlic Z, Nunez M, Weber A, Azurmendi P, Schultze-Seemann W, Werner M, Neumann HP. Jilg CA, et al. Among authors: erlic z. Nephron Clin Pract. 2013;123(1-2):13-21. doi: 10.1159/000351049. Epub 2013 Jun 4. Nephron Clin Pract. 2013. PMID: 23752029

2

When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?

Erlic Z, Neumann HP. Erlic Z, et al. Clin Endocrinol (Oxf). 2009 Mar;70(3):354-7. doi: 10.1111/j.1365-2265.2008.03480.x. Epub 2008 Dec 3. Clin Endocrinol (Oxf). 2009. PMID: 19067729

3

Familial pheochromocytoma.

Erlic Z, Neumann HP. Erlic Z, et al. Hormones (Athens). 2009 Jan-Mar;8(1):29-38. doi: 10.14310/horm.2002.1219. Hormones (Athens). 2009. PMID: 19269919 Free article.

4

Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.

Weber A, Hoffmann MM, Neumann HP, Erlic Z. Weber A, et al. Among authors: erlic z. Horm Cancer. 2012 Aug;3(4):187-92. doi: 10.1007/s12672-012-0113-y. Epub 2012 May 10. Horm Cancer. 2012. PMID: 22573489 Free PMC article.

5

Systematic comparison of sporadic and syndromic pancreatic islet cell tumors.

Erlic Z, Ploeckinger U, Cascon A, Hoffmann MM, von Duecker L, Winter A, Kammel G, Bacher J, Sullivan M, Isermann B, Fischer L, Raffel A, Knoefel WT, Schott M, Baumann T, Schaefer O, Keck T, Baum RP, Milos I, Muresan M, Peczkowska M, Januszewicz A, Cupisti K, Tönjes A, Fasshauer M, Langrehr J, von Wussow P, Agaimy A, Schlimok G, Lamberts R, Wiech T, Schmid KW, Weber A, Nunez M, Robledo M, Eng C, Neumann HP; VHL-ICT Consortium; German NET Registry. Erlic Z, et al. Endocr Relat Cancer. 2010 Oct 5;17(4):875-83. doi: 10.1677/ERC-10-0037. Print 2010 Dec. Endocr Relat Cancer. 2010. PMID: 20660572

6

Evidence of MEN-2 in the original description of classic pheochromocytoma.

Neumann HP, Vortmeyer A, Schmidt D, Werner M, Erlic Z, Cascon A, Bausch B, Januszewicz A, Eng C. Neumann HP, et al. Among authors: erlic z. N Engl J Med. 2007 Sep 27;357(13):1311-5. doi: 10.1056/NEJMoa071407. N Engl J Med. 2007. PMID: 17898100 Free article.

7

Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.

Sullivan M, Erlic Z, Hoffmann MM, Arbeiter K, Patzer L, Budde K, Hoppe B, Zeier M, Lhotta K, Rybicki LA, Bock A, Berisha G, Neumann HP. Sullivan M, et al. Among authors: erlic z. Ann Hum Genet. 2010 Jan;74(1):17-26. doi: 10.1111/j.1469-1809.2009.00554.x. Ann Hum Genet. 2010. PMID: 20059470 Free article.

8

Maternal transmission of symptomatic disease with SDHD mutation: fact or fiction?

Neumann HP, Erlic Z. Neumann HP, et al. Among authors: erlic z. J Clin Endocrinol Metab. 2008 May;93(5):1573-5. doi: 10.1210/jc.2008-0569. J Clin Endocrinol Metab. 2008. PMID: 18463350 No abstract available.

9

Diagnosing patients with hereditary paraganglial tumours.

Erlic Z, Neumann HP. Erlic Z, et al. Lancet Oncol. 2009 Aug;10(8):741. doi: 10.1016/S1470-2045(09)70204-9. Lancet Oncol. 2009. PMID: 19647193 Review. No abstract available.

10

Multiple endocrine neoplasia type 2.

Wohllk N, Schweizer H, Erlic Z, Schmid KW, Walz MK, Raue F, Neumann HP. Wohllk N, et al. Among authors: erlic z. Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):371-87. doi: 10.1016/j.beem.2010.02.001. Best Pract Res Clin Endocrinol Metab. 2010. PMID: 20833330 Review.

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