Genetic and clinical features of multiple endocrine neoplasia types 1 and 2. (Q41667928)

6 October 2017

Genetic and clinical features of multiple endocrine neoplasia types 1 and 2. (English)

1 reference

multiple endocrine neoplasia

6 October 2017

1 reference

4

R Elisei

1 reference

6 October 2017

C Romei

1

1 reference

PMCID

3503399

6 October 2017

E Pardi

series ordinal

2

1 reference

PMCID

3503399

6 October 2017

F Cetani

series ordinal

3

1 reference

6 October 2017

8 November 2012

1 reference

6 October 2017

1 reference

6 October 2017

2012

1 reference

6 October 2017

705036

1 reference

Creative Commons Attribution 3.0 Unported

6 October 2017

start time

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

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6 June 2018

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6 June 2018

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6 June 2018

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6 June 2018

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6 June 2018

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Familial isolated primary hyperparathyroidism--a multiple endocrine neoplasia type 1 variant?

6 June 2018

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Multiple endocrine neoplasia type 1: new clinical and basic findings

6 June 2018

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A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

6 June 2018

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Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

6 June 2018

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Pheochromocytoma: inherited associations, bilaterality, and cortex preservation

6 June 2018

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Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis

6 June 2018

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Intraoperative parathormone measurement in patients with multiple endocrine neoplasia type I syndrome and hyperparathyroidism

6 June 2018

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Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.

6 June 2018

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

6 June 2018

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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

6 June 2018

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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

6 June 2018

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Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.

6 June 2018

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Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma

6 June 2018

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Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

6 June 2018

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A calcitonin-secreting medullary thyroid carcinoma associated with mucosal neuromas, marfanoid features, myopathy and pigmentation

6 June 2018

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Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

6 June 2018

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Magnetic resonance imaging versus endoscopic ultrasonography for the detection of pancreatic tumours in multiple endocrine neoplasia type 1.

6 June 2018

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In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.

18 August 2018

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18 August 2018

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RET genetic screening of sporadic medullary thyroid cancer (MTC) allows the preclinical diagnosis of unsuspected gene carriers and the identification of a relevant percentage of hidden familial MTC (FMTC).

18 August 2018

1 reference

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Surgery for multiple endocrine neoplasia type 1-associated primary hyperparathyroidism

18 August 2018

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The MENX syndrome and p27: relationships with multiple endocrine neoplasia.

18 August 2018

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Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes

18 August 2018

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Risk factors and causes of death in MEN1 disease. A GTE (Groupe d'Etude des Tumeurs Endocrines) cohort study among 758 patients

18 August 2018

1 reference

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Sporadic and MEN1-related primary hyperparathyroidism: differences in clinical expression and severity

18 August 2018

1 reference

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Premonitory symptoms preceding metastatic medullary thyroid cancer in MEN 2B: An exploratory analysis.

18 August 2018

1 reference

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Pheochromocytoma in MEN 2A syndrome. Study of 54 patients

18 August 2018

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Natural course of small adrenal lesions in multiple endocrine neoplasia type 1: an endoscopic ultrasound imaging study

18 August 2018

1 reference

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RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center

18 August 2018

1 reference

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Ret proto-oncogene mutations in apparently sporadic Turkish medullary thyroid carcinoma patients: Turkmen study

18 August 2018

1 reference

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A new germline RET mutation apparently devoid of transforming activity serendipitously discovered in a patient with atrophic autoimmune thyroiditis and primary ovarian failure.

18 August 2018

1 reference

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Meningiomas may be a component tumor of multiple endocrine neoplasia type 1.

18 August 2018

1 reference

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Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation.

18 August 2018

1 reference

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Familial multiple endocrine neoplasia syndromes: components, classification, and nomenclature.

18 August 2018

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Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3503399

Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up.

18 August 2018

1 reference

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Familial medullary thyroid carcinoma without associated endocrinopathies: a distinct clinical entity

18 August 2018

1 reference

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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

3 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2012%2F705036

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group

21 January 2018

1 reference

12 December 2020

Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918

1 reference

12 December 2020

Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism

1 reference

12 December 2020

Surgical treatment of medullary thyroid carcinoma

1 reference

12 December 2020

Results of initial operation for hyperparathyroidism in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Single access retroperitoneoscopic adrenalectomy (SARA)--one step beyond in endocrine surgery

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12 December 2020

Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis

1 reference

12 December 2020

Familial cutaneous lichen amyloidosis in association with multiple endocrine neoplasia type 2A: a new variant

1 reference

12 December 2020

Molecular pathogenesis of primary hyperparathyroidism

1 reference

12 December 2020

Achieving eugastrinemia in MEN1 patients: both duodenal inspection and formal lymph node dissection are important

1 reference

12 December 2020

Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2

1 reference

12 December 2020

Sipple's syndrome: medullary thyroid carcinoma, pheochromocytoma, and parathyroid disease. Studies in a large family. NIH conference

1 reference

12 December 2020

The surgical management of medullary thyroid carcinoma

1 reference

12 December 2020

Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1

1 reference

12 December 2020

Increased risk of lymph node metastasis in multifocal hereditary and sporadic medullary thyroid cancer

1 reference

12 December 2020

Is total parathyroidectomy the treatment of choice for hyperparathyroidism in multiple endocrine neoplasia type 1?

1 reference

12 December 2020

Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile

1 reference

12 December 2020

Multiple endocrine neoplasia type 2

1 reference

12 December 2020

Preoperative localizing studies for initial parathyroidectomy in MEN1 syndrome: is there any benefit?

1 reference

12 December 2020

Multiple endocrine neoplasia type 2 syndromes: historical perspectives

1 reference

12 December 2020

A French Canadian family with multiple endocrine neoplasia type 2 syndromes

1 reference

12 December 2020

Familial Medullary Thyroid Carcinoma with Noncysteine RET Mutations: Phenotype-Genotype Relationship in a Large Series of Patients

1 reference

12 December 2020

Identifiers

DOI

10.1155/2012/705036

1 reference

6 October 2017

1 reference

6 October 2017

1 reference

PMCID

3503399