review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0960-7404(01)00031-7 |
P698 | PubMed publication ID | 12356510 |
P2093 | author name string | Sally E Carty | |
Matthew J Glascock | |||
P2860 | cites work | Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription | Q22001458 |
Positional cloning of the gene for multiple endocrine neoplasia-type 1 | Q28307577 | ||
Duodenopancreatic resections in patients with multiple endocrine neoplasia type 1. | Q33921582 | ||
Genetic aspects of adenomatosis of endocrine glands | Q34234754 | ||
Forty-year appraisal of gastrinoma. Back to the future | Q40971301 | ||
Zollinger-Ellison syndrome can be the initial endocrine manifestation in patients with multiple endocrine neoplasia-type I. | Q41012844 | ||
Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1. | Q41014429 | ||
Pancreatic lesions and hormonal profile of pancreatic tumors in multiple endocrine neoplasia type I. An immunocytochemical study of nine patients | Q41785102 | ||
Pancreatic polypeptide is a useful plasma marker for radiographically evident pancreatic islet cell tumors in patients with multiple endocrine neoplasia type 1. | Q42449253 | ||
Multiple Endocrine Neoplasia Type 1: A 10-Year Prospective Screening Study in Four Kindreds* | Q42464524 | ||
Intraoperative parathormone measurement in patients with multiple endocrine neoplasia type I syndrome and hyperparathyroidism | Q42487338 | ||
Clinical, anatomical, and evolutive features of patients with the Zollinger-Ellison syndrome combined with type I multiple endocrine neoplasia. | Q42497648 | ||
Multiple endocrine syndrome type I. Clinical, laboratory findings, and management in five families | Q44494038 | ||
Surgery in Zollinger-Ellison syndrome alters the natural history of gastrinoma | Q44748811 | ||
Screening for multiple endocrine neoplasia type 1 in patients with recognized pituitary adenoma | Q45115400 | ||
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma | Q48100816 | ||
Results of treatment of pituitary disease in multiple endocrine neoplasia, type I. | Q48953134 | ||
Adrenal lesion in multiple endocrine neoplasia type 1. | Q50593991 | ||
Cost effectiveness of EUS for preoperative localization of pancreatic endocrine tumors. | Q51483627 | ||
Surgery for asymptomatic pancreatic lesion in multiple endocrine neoplasia type I. | Q52887975 | ||
Multiple endocrine neoplasia syndromes | Q62978448 | ||
Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome | Q68084123 | ||
The natural history of multiple endocrine neoplasia type 1. Highly uncommon or highly unrecognized? | Q68309763 | ||
Screening for the multiple endocrine neoplasia syndrome type I. A study of 11 kindreds in The Netherlands | Q69377250 | ||
Parathyroid mitogenic activity in plasma from patients with familial multiple endocrine neoplasia type 1 | Q69881030 | ||
Hyperparathyroidism presenting as the first lesion in multiple endocrine neoplasia type 1 | Q69897298 | ||
Total pancreatectomy in the MEN-1 syndrome | Q69914931 | ||
Vocal cord paralysis and reoperative parathyroidectomy. A prospective study | Q70025690 | ||
Long-term evaluation of patients with primary parathyroid hyperplasia managed by total parathyroidectomy and heterotopic autotransplantation | Q71349807 | ||
Prospective study of surgical resection of duodenal and pancreatic gastrinomas in multiple endocrine neoplasia type 1 | Q71568271 | ||
Clinical studies of multiple endocrine neoplasia type 1 (MEN1) | Q71777163 | ||
Surgical management of insulinoma associated with multiple endocrine neoplasia type I | Q72179249 | ||
Cause of death in multiple endocrine neoplasia type 1 | Q72220849 | ||
Determinants of metastatic rate and survival in patients with Zollinger-Ellison syndrome: a prospective long-term study | Q72281843 | ||
A new approach to parathyroidectomy | Q72425046 | ||
Results of heterotopic parathyroid autotransplantation: a 13-year experience | Q73272722 | ||
Screening for MEN1 mutations in patients with atypical endocrine neoplasia | Q73272733 | ||
Pancreaticoduodenal endocrine tumors in multiple endocrine neoplasia type 1: surgery or surveillance? | Q73292276 | ||
Malignant endocrine tumors in patients with MEN 1 disease | Q73375839 | ||
Lethality of multiple endocrine neoplasia type I | Q74580275 | ||
Thymic carcinoids in multiple endocrine neoplasia type 1 | Q74791955 | ||
Current concepts in the surgical management of multiple endocrine neoplasia type 1 pancreatic-duodenal disease. Results in the treatment of 40 patients with Zollinger-Ellison syndrome, hypoglycaemia or both | Q74817194 | ||
ENDOCRINE ADENOMATOSIS AND PEPTIC ULCER IN A LARGE KINDRED. INHERITED MULTIPLE TUMORS AND MOSAIC PLEIOTROPISM IN MAN | Q76538221 | ||
The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1 | Q77687457 | ||
P433 | issue | 3 | |
P921 | main subject | multiple endocrine neoplasia | Q1553018 |
multiple endocrine neoplasia type 1 | Q3347154 | ||
P304 | page(s) | 143-150 | |
P577 | publication date | 2002-11-01 | |
P1433 | published in | Surgical Oncology | Q14421678 |
P1476 | title | Multiple endocrine neoplasia type 1: fresh perspective on clinical features and penetrance | |
P478 | volume | 11 |
Q36004168 | Endocrine tumor syndromes in infancy and childhood |
Q24679314 | Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans |
Q37146881 | Inherited endocrinopathies: an update |
Q36389423 | Intestinal neuroendocrine tumor in a patient with pituitary adenoma. A case report and review of the current screening recommendations |
Q79775310 | MEN1 family with a novel frameshift mutation |
Q39412594 | Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood |
Q34098952 | Multiple carcinoids in the duodenum, pancreas and stomach accompanied with type A gastritis: a case report |
Q38752172 | Pancreatic neuroendocrine tumors in MEN1 disease: a mono-centric longitudinal and prognostic study |
Q51830527 | Reverse referral: from pathology to endocrinology. |
Q37670702 | Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age? |
Q42418247 | Simultaneous EUS-FNA Diagnosis and TNM Staging of a Pancreatic Neuroendocrine Tumor in a Patient with an Unrecognized MEN Type 1. |
Q38053116 | Surgery for a gastroenteropancreatic neuroendocrine tumor (GEPNET) in multiple endocrine neoplasia type 1. |
Q35571396 | The role of genetics in the surgical management of familial endocrinopathy syndromes |
Q39994289 | Thymic neuroendocrine tumors in multiple endocrine neoplasia type 1: a comparative study on 21 cases among a series of 761 MEN1 from the GTE (Groupe des Tumeurs Endocrines). |
Q44943256 | Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene |
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