(Q40465055)

English

Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma.

scientific article published on 5 October 2015

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

phaeochromocytoma

1 reference

based on heuristic

inferred from title

genotype-phenotype correlation

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

object named as

Sendhil Rajan

1

0 references

author name string

Ghazala Zaidi

2

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Anjali Mishra

4

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Amit Agarwal

5

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Saroj Kanta Mishra

6

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Eesh Bhatia

7

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

publication date

5 October 2015

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

World Journal of Surgery

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

40

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

690-696

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

https://scigraph.springernature.com/pub.10.1007/s00268-015-3255-6

0 references

Pheochromocytoma: state-of-the-art and future prospects

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Familial pheochromocytomas and paragangliomas

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Size of the tumor and pheochromocytoma of the adrenal gland scaled score (PASS): can they predict malignancy?

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Multiple endocrine neoplasia type 2 RET protooncogene database: repository of MEN2-associated RET sequence variation and reference for genotype/phenotype correlations.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Prevalence of common disease-associated variants in Asian Indians.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Genotype-Phenotype Correlations by Ethnicity and Mutation Location in BRCA Mutation Carriers

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

RET gene mutations and polymorphisms in medullary thyroid carcinomas in Indian patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Molecular analysis of the RET proto-oncogene key exons in patients with medullary thyroid carcinoma: a comprehensive study of the Iranian population.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Prophylactic thyroidectomy for MEN 2-related medullary thyroid carcinoma based on predictive testing for RET proto-oncogene mutation and basal serum calcitonin in China

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

High penetrance of pheochromocytoma in multiple endocrine neoplasia 2 caused by germ line RET codon 634 mutation in Japanese patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Bilateral Pheochromocytomas in MEN2A Syndrome: A Two-Institution Experience

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Clinical experiences of pheochromocytoma in Korea.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Pheochromocytoma in children and adolescents

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Pediatric and adolescent pheochromocytoma: clinical presentation and outcome of surgery

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Diagnosis of endocrine disease: Biochemical diagnosis of phaeochromocytoma and paraganglioma

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Genotype-phenotype correlation in multiple endocrine neoplasia type 2

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00268-015-3255-6

21 January 2018

Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series

1 reference

https://pubmed.ncbi.nlm.nih.gov/26438242

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/26438242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26438242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations seen among patients with pheochromocytoma and paraganglioma at a referral center from India.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26438242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B

1 reference

https://pubmed.ncbi.nlm.nih.gov/26438242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00268-015-3255-6

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

ResearchGate publication ID

0 references

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