Multiple Endocrine Neoplasia type 1 (MEN1) is a rare syndrome caused by mutations in the MEN1 gene on chromosome 11. It is characterized by the occurrence of primary hyperparathyroidism (pHPT), duodenopancreatic neuroendocrine tumours (NET), pituitary tumours, adrenal adenomas and NET of the stomach, bronchus and thymus. The research in this thesis focusses on the long-term outcome of MEN1 related manifestations. Since the discovery of the MEN1 gene in 1997, presymptomatic genetic testing became available. In the research described in chapter 3 we show that patients with a genetic diagnosis had less manifestations at the end of follow-up and no MEN1 related malignancy or death, compared to patients with a clinical MEN1 diagnosis. Primary hy...
Multiple endocrine neoplasia (MEN) describes the occurrence of tumours affecting two or more endocri...
CONTEXT: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disease ...
Multiple endocrine neoplasia syndromes have since been classified as types 1 and 2, each with specif...
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare syndrome caused by mutations in the MEN1 gene o...
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare syndrome caused by mutations in the MEN1 gene o...
Multiple Endocrine Neoplasia type1 (MEN1) is a rare autosomal inherited disorder, characterized by t...
Multiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the MEN1 gene on...
OBJECTIVE: To identify the optimal surgical strategy for multiple endocrine neoplasia type 1 (MEN1)-...
Multiple endocrine neoplasia (MEN) are clinical inherited syndromes affecting different endocrine gl...
International audienceMultiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by...
Multiple endocrine neoplasia-1 (MEN-1) is an autosomal dominant inherited syndrome that occurs due t...
Multiple Endocrine Neoplasia (MEN) syndromes are rare, hereditary diseases, predisposing to the deve...
The MEN1 syndrome is a hereditary disease characterized by the simultaneous occurrence of parathyroi...
Introduction: Mutation testing for the MEN1 gene is a useful method to diagnose and predict individu...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the oc...
Multiple endocrine neoplasia (MEN) describes the occurrence of tumours affecting two or more endocri...
CONTEXT: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disease ...
Multiple endocrine neoplasia syndromes have since been classified as types 1 and 2, each with specif...
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare syndrome caused by mutations in the MEN1 gene o...
Multiple Endocrine Neoplasia type 1 (MEN1) is a rare syndrome caused by mutations in the MEN1 gene o...
Multiple Endocrine Neoplasia type1 (MEN1) is a rare autosomal inherited disorder, characterized by t...
Multiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the MEN1 gene on...
OBJECTIVE: To identify the optimal surgical strategy for multiple endocrine neoplasia type 1 (MEN1)-...
Multiple endocrine neoplasia (MEN) are clinical inherited syndromes affecting different endocrine gl...
International audienceMultiple endocrine neoplasia type 1 (MEN1) is a rare syndrome characterized by...
Multiple endocrine neoplasia-1 (MEN-1) is an autosomal dominant inherited syndrome that occurs due t...
Multiple Endocrine Neoplasia (MEN) syndromes are rare, hereditary diseases, predisposing to the deve...
The MEN1 syndrome is a hereditary disease characterized by the simultaneous occurrence of parathyroi...
Introduction: Mutation testing for the MEN1 gene is a useful method to diagnose and predict individu...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the oc...
Multiple endocrine neoplasia (MEN) describes the occurrence of tumours affecting two or more endocri...
CONTEXT: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disease ...
Multiple endocrine neoplasia syndromes have since been classified as types 1 and 2, each with specif...