Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary
cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and …

… multiple endocrine neoplasia type 2A have a 20–30% risk for primary hyperparathyroidism.
Individuals with multiple endocrine neoplasia type 2B … of multiple endocrine neoplasia type 2, …

… for novel therapeutical interventions in multiple endocrine neoplasia type 1 (MEN1) …
Schematic representation of epigenetic regulation in multiple endocrine neoplasia type 1 (MEN1)-…

… [Adapted from PJ Newey and RV Thakker: Role of multiple endocrine neoplasia type 1
mutational analysis in clinical practice. Endocr Pract 17(Suppl 3):8–17, 2011 (21), with permission…

… A few years ago a novel multiple endocrine neoplasia syndrome, named multiple endocrine
neoplasia type 4 (MEN4), was discovered thanks to studies conducted on a MEN syndrome …

Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by the co-occurrence
of primary hyperparathyroidism, duodenopancreatic neuroendocrine tumours (NETs…

Multiple endocrine neoplasia type 2 (MEN2) is a autosomal dominat inherited tumour-syndrome
caused by germline activating mutations of the RET proto-oncogene on chromosome 10…

… of m-calpain as the multiple endocrine neoplasia type 1 gene. Hum … Multiple endocrine
neoplasia type 1 gene maps to … in screening for multiple endocrine neoplasia type 1. Endocrinol …

… as von Hippel-Lindau disease or multiple endocrine neoplasia type 1 in which the clinical
… data may be, in particular, interesting for syndromes such as multiple endocrine neoplasias. …

Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited syndrome caused by inactivating
heterozygote mutations of the MEN1 gene affecting parathyroid glands, neuroendocrine …