| P2093 | author name string | M Cristina Pacheco | |
| P2860 | cites work | Multiple tumor suppressor pathways negatively regulate telomerase | Q24306608 |
| | Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans | Q24679314 |
| | Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene | Q28249576 |
| | Activation of a novel human transforming gene, ret, by DNA rearrangement | Q28286635 |
| | Positional cloning of the gene for multiple endocrine neoplasia-type 1 | Q28307577 |
| | Menin induces apoptosis in murine embryonic fibroblasts | Q28589504 |
| | Gastrointestinal manifestations of multiple endocrine neoplasia type 2. | Q33425148 |
| | Guidelines for diagnosis and therapy of MEN type 1 and type 2. | Q34104591 |
| | Role of multiple endocrine neoplasia type 1 mutational analysis in clinical practice | Q34174705 |
| | Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). | Q34283436 |
| | Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma | Q34468665 |
| | Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d’étude des Tumeurs Endocrines (GTE) cohort study | Q61647410 |
| | Recessive transmission of a multiple endocrine neoplasia syndrome in the rat | Q63951641 |
| | Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome | Q68084123 |
| | Physiologic versus neoplastic C-cell hyperplasia of the thyroid: separation of distinct histologic and biologic entities | Q71046691 |
| | Sporadic versus familial medullary thyroid microcarcinoma: a histopathologic study of 50 consecutive patients | Q77101999 |
| | Multiple endocrine neoplasia type 2B diagnosed on suction rectal biopsy in infancy: a report of 2 cases | Q79813985 |
| | Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patients | Q80775138 |
| | Multiple endocrine neoplasia type 1 parathyroid adenoma development over time | Q80874213 |
| | Adrenal cortical tumors, pheochromocytomas and paragangliomas | Q83760021 |
| | MEN1 disease occurring before 21 years old: a 160-patient cohort study from the Groupe d'étude des Tumeurs Endocrines | Q86546147 |
| | Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds | Q34504187 |
| | C-cell hyperplasia and medullary thyroid microcarcinoma | Q34577310 |
| | A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization | Q34635679 |
| | A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. | Q34649802 |
| | Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas | Q34758456 |
| | Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions. | Q35929598 |
| | Identification of MEN1 gene mutations in families with MEN 1 and related disorders | Q36622013 |
| | The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations | Q36735215 |
| | Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors | Q37056120 |
| | Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states | Q37198026 |
| | Histopathologic and clinical features of medullary microcarcinoma and C-cell hyperplasia in prophylactic thyroidectomies for medullary carcinoma: a study of 42 cases | Q37314128 |
| | MEN1 gene and its mutations: basic and clinical implications | Q37345051 |
| | New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis. | Q37575861 |
| | Pheochromocytoma and paraganglioma syndromes: genetics and management update. | Q37577699 |
| | MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27Kip1 and p18INK4C) mutations | Q37787565 |
| | Neuroendocrine tumors of the pancreas: current concepts and controversies. | Q38178882 |
| | RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma | Q38202024 |
| | The association between Hirschsprung's disease and multiple endocrine neoplasia type 2a: a systematic review | Q38223912 |
| | Multiple endocrine neoplasia syndromes 1 and 2: manifestations and management in childhood and adolescence | Q38411934 |
| | A randomized, prospective trial of operative treatments for hyperparathyroidism in patients with multiple endocrine neoplasia type 1. | Q38447520 |
| | Transfection of the multiple endocrine neoplasia type 1 gene to a human endocrine pancreatic tumor cell line inhibits cell growth and affects expression of JunD, delta-like protein 1/preadipocyte factor-1, proliferating cell nuclear antigen, and QM/ | Q40559040 |
| | Low frequency of germline mutations in the RET proto‐oncogene in patients with apparently sporadic medullary thyroid carcinoma | Q40980321 |
| | The ret proto-oncogene is consistently expressed in human pheochromocytomas and thyroid medullary carcinomas | Q41720815 |
| | Pathogenesis of gastrinomas associated with multiple endocrine neoplasia type 1. | Q42424883 |
| | C-cell hyperplasia and medullary thyroid carcinoma: clinicopathological and genetic correlations in 66 consecutive patients | Q42446151 |
| | Presymptomatic thyroidectomy in multiple endocrine neoplasia 2a. | Q42487300 |
| | Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome | Q42576314 |
| | Risk factors and causes of death in MEN1 disease. A GTE (Groupe d'Etude des Tumeurs Endocrines) cohort study among 758 patients | Q44301609 |
| | Incidence and location of ectopic abnormal parathyroid glands | Q44405196 |
| | Frequent association between MEN 2A and cutaneous lichen amyloidosis | Q44514148 |
| | Familial medullary thyroid carcinoma associated with cutaneous lichen amyloidosis. | Q46010186 |
| | Primary lymph node gastrinoma or occult duodenal microgastrinoma with lymph node metastases in a MEN1 patient: the need for a systematic search for the primary tumor | Q46562102 |
| | RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center | Q46982081 |
| | Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia | Q48079288 |
| | Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma. | Q50890372 |
| | Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors. | Q51420518 |
| | Higher risk of aggressive pancreatic neuroendocrine tumors in MEN1 patients with MEN1 mutations affecting the CHES1 interacting MENIN domain. | Q54323177 |
| | A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome. | Q54353310 |
| | Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype. | Q54546392 |
| | Premonitory symptoms preceding metastatic medullary thyroid cancer in MEN 2B: An exploratory analysis. | Q54784797 |
| | A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 | Q55670968 |
| | Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage | Q57319205 |
| | Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene | Q60021403 |
| P433 | issue | 2 | |
| P921 | main subject | multiple endocrine neoplasia | Q1553018 |
| P304 | page(s) | 89-97 | |
| P577 | publication date | 2016-03-09 | |
| P1433 | published in | Journal of Pediatric Genetics | Q27724414 |
| P1476 | title | Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes | |
| P478 | volume | 5 | |