(Q54773654)

English

Penetrance of inherited medullary thyroid carcinoma and genotype-phenotype correlation in a large multiple endocrine neoplasia type 2A family with C634Y RET mutation.

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scholarly article

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Penetrance of inherited medullary thyroid carcinoma and genotype-phenotype correlation in a large multiple endocrine neoplasia type 2A family with C634Y RET mutation. (English)

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

genotype-phenotype correlation

1 reference

based on heuristic

inferred from title

thyroid carcinoma

1 reference

based on heuristic

inferred from title

multiple endocrine neoplasia type 2A

1 reference

based on heuristic

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author name string

Beatriz González-Yebra

1

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

María Elena Medrano

2

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Alejandra Mantilla

3

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Virginia Palma

4

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Carmen Colin

5

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Dulce María Hernández

6

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

José Tapia

7

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Brian Dawson

8

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Mauricio Salcedo

9

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

publication date

1 January 2003

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Endocrine Pathology

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

14

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

1

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

71-80

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

https://scigraph.springernature.com/pub.10.1385/ep:14:1:71

0 references

Current perspectives on the diagnosis and management of patients with multiple endocrine neoplasia type 2 syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à Calcitonine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large family

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ line mutation analysis in families with multiple endocrine neoplasia type 2A or familial medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presentation of a kindred with familial medullary thyroid carcinoma and Cys611Phe mutation of the RET proto-oncogene demonstrating low grade malignancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alcohol-stimulated calcitonin release in medullary carcinoma of the thyroid

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

One gene—four syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET proto-oncogene mutations in French MEN 2A and FMTC families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical and screening age-at-onset distribution for the MEN-2 syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age-Related Disease Penetrance in a Large Medullary Thyroid Cancer Family With a Codon 609 RET Gene Mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Whisky: a new provacative test for calcitonin secretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic aspects of multiple endocrine neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET mutations in exons 13 and 14 of FMTC patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young children

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial medullary thyroid carcinoma with noncysteine ret mutations: phenotype-genotype relationship in a large series of patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advances and controversies in the diagnosis and management of medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and management of pheochromocytomas in patients with multiple endocrine neoplasia type 2-relevance of specific mutations in the RET proto-oncogene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The RET proto‐oncogene and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12746565

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1385/EP:14:1:71

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

3 June 2018

http://europepmc.org/abstract/MED/12746565

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