(Q42491436)

English

Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis

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scholarly article

1 reference

Europe PubMed Central

1 November 2017

Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis (English)

1 reference

Europe PubMed Central

1 November 2017

multiple endocrine neoplasia type 2A

1 reference

based on heuristic

inferred from title

Isabella Ceccherini

object named as

I Ceccherini

1

0 references

author name string

C Romei

2

1 reference

Europe PubMed Central

1 November 2017

V Barone

3

1 reference

Europe PubMed Central

1 November 2017

F Pacini

4

1 reference

Europe PubMed Central

1 November 2017

E Martino

5

1 reference

Europe PubMed Central

1 November 2017

A Loviselli

6

1 reference

Europe PubMed Central

1 November 2017

A Pinchera

7

1 reference

Europe PubMed Central

1 November 2017

G Romeo

8

1 reference

Europe PubMed Central

1 November 2017

publication date

1 March 1994

1 reference

Europe PubMed Central

1 November 2017

Journal of Endocrinological Investigation

1 reference

Europe PubMed Central

1 November 2017

17

1 reference

Europe PubMed Central

1 November 2017

3

1 reference

Europe PubMed Central

1 November 2017

201-204

1 reference

Europe PubMed Central

1 November 2017

https://scigraph.springernature.com/pub.10.1007/bf03347719

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Hereditary localized pruritus in affected members of a kindred with multiple endocrine neoplasia type 2A (Sipple's syndrome).

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Primary localized cutaneous amyloidosis and familial medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis: description of a new family.

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Exon structure and flanking intronic sequences of the human RET proto-oncogene

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

How sensitive is PCR-SSCP?

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Epidemiology of primary cutaneous amyloidoses in southeast Asia

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Epidemiology of primary cutaneous amyloidoses in South America

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF03347719

21 January 2018

Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker

1 reference

https://pubmed.ncbi.nlm.nih.gov/7914213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7914213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/7914213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Friction amyloidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7914213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7914213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03347719

1 reference

Europe PubMed Central

1 November 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

1 November 2017

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