(Q42469941)

English

Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634.

scientific article published on 4 November 2004

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scholarly article

1 reference

Europe PubMed Central

1 November 2017

Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634. (English)

1 reference

Europe PubMed Central

1 November 2017

8

object named as

Henning Dralle

1 reference

Europe PubMed Central

1 November 2017

author name string

Oliver Gimm

1

1 reference

Europe PubMed Central

1 November 2017

Jörg Ukkat

2

1 reference

Europe PubMed Central

1 November 2017

Barbara E Niederle

3

1 reference

Europe PubMed Central

1 November 2017

Theresa Weber

4

1 reference

Europe PubMed Central

1 November 2017

Phuong Nguyen Thanh

5

1 reference

Europe PubMed Central

1 November 2017

Michael Brauckhoff

6

1 reference

Europe PubMed Central

1 November 2017

Bruno Niederle

7

1 reference

Europe PubMed Central

1 November 2017

publication date

4 November 2004

1 reference

Europe PubMed Central

1 November 2017

World Journal of Surgery

1 reference

Europe PubMed Central

1 November 2017

28

1 reference

Europe PubMed Central

1 November 2017

1312-1316

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Europe PubMed Central

1 November 2017

12

1 reference

Europe PubMed Central

1 November 2017

https://scigraph.springernature.com/pub.10.1007/s00268-004-7640-9

0 references

Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morbidity of prophylactic lymph node dissection in the central neck area in patients with papillary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET proto-oncogene mutations affecting codon 790/791: A mild form of multiple endocrine neoplasia type 2A syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complications of neck dissection for thyroid cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The different RET-activating capability of mutations of cysteine 620 or cysteine 634 correlates with the multiple endocrine neoplasia type 2 disease phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET codon 634 mutations in multiple endocrine neoplasia type 2: variable clinical features and clinical outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 2: evaluation of the genotype-phenotype relationship.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk estimation and screening in families of patients with medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Review of multiple endocrine neoplasia type 2A in children: therapeutic results of early thyroidectomy and prognostic value of codon analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prognostic value of codon 918 (ATG-->ACG) RET proto-oncogene mutations in sporadic medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early or prophylactic thyroidectomy in MEN 2/FMTC gene carriers: results in 71 thyroidectomized patients. The French Calcitonin Tumours Study Group (GETC).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RET.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medullary carcinoma in children. Results of early detection and surgery

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic insights into familial cancers-- update and recent discoveries

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/15517481

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/15517481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00268-004-7640-9

1 reference

Europe PubMed Central

1 November 2017

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0 references

1 reference

Europe PubMed Central

1 November 2017

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