List of works by Zoran Erlic

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

scientific article published on 04 June 2013

Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients

scientific article

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

scientific article published on 7 April 2009

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

scientific article published on September 2007

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

scientific article published in February 2008

Familial nonsyndromic pheochromocytoma.

scientific article published in August 2006

Familial pheochromocytoma.

scientific article published in January 2009

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

scientific article published in May 2008

Metabolic Alterations in Patients with Pheochromocytoma

scientific article published on 16 July 2018

Metabolic impact of pheochromocytoma/paraganglioma: targeted metabolomics in patients before and after tumor removal

scientific article published on 01 December 2019

Multiple endocrine neoplasia type 2

scientific article published on 01 June 2010

Neurofibromatosis type 1: should we screen for other genetic syndromes? A case report of co-existence with multiple endocrine neoplasia 2A.

scientific article published on 25 June 2009

Paraganglioma syndrome: SDHB, SDHC, and SDHD mutations in head and neck paragangliomas

scientific article published on 01 August 2006

Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.

scientific article published on 6 October 2009

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome

scientific article

Pheochromocytoma - still a challenge

scientific article

RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma.

scientific article published on 12 June 2015

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10.

scientific article

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

scientific article published on 10 May 2012

Systematic comparison of sporadic and syndromic pancreatic islet cell tumors

scientific article published on 5 October 2010

The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression

scientific article published on 28 March 2012

The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome

scientific article published on 14 March 2009

[CME Answers/"Pheochromocytoma in the General Practice", Praxis No. 17-18]

scientific article published on 01 September 2018

[CME: Pheochromocytoma in the General Practice]

scientific article published on 01 August 2018

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