Searchable abstracts of presentations at key conferences in endocrinology

ea0031s1.3 | Irn bru, to drink or not to drink: endocrinology and iron | SFEBES2013

The celtic disease – haemochromatosis: a disease of iron overload

Zoller Heinz , Schranz Melanie

In contrast to the conventional view of haemochromatosis as a monogenic disease with autosomal recessive inheritance, more recent evidence form genetic, epidemiological, cell biological and clinical studies, challenges this view. The concept that haemochromatosis is an endocrine disorder of mixed etiology embraces the poylgenic nature of the disease, the low penetrance and the similarities in phenotype of genetic and acquired forms of iron overload. Key to understanding haemoc...

ea0035p861 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Serum prolactin in advanced chronic liver disease

Ress Claudia , Maeser Pirmin , Tschoner Alexander , Loacker Lorin , Salzmann Karin , Staudacher Gabriele , Melmer Andreas , Zoller Heinz , Vogel Wolfgang , Griesmacher Andrea , Tilg Herbert , Graziadei Ivo , Kaser Susanne

Introduction: Hyperprolactinemia is a frequent endocrine disorder with well known harmful effects on the reproductive system and bone metabolism. Besides prolactinomas several drugs and disorders such as renal failure and hypothyroidism have been shown to cause hyperprolactinemia. Based on former studies liver cirrhosis has also been suggested to cause hyperprolactinemia while mechanisms have not been identified yet. In this study we set out to investigate the prevalence and p...