(Q35636304)

9 August 2017

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title

Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman (English)

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multiple endocrine neoplasia

9 August 2017

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Andreas Weinhäusel

1

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9 August 2017

Annemarie Behmel

2

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9 August 2017

Bruce A J Ponder

3

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9 August 2017

Oskar A Haas

4

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9 August 2017

Bruno Niederle

5

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9 August 2017

Alois Gessl

6

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9 August 2017

Heinrich Vierhapper

7

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9 August 2017

Roswitha Pfragner

8

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9 August 2017

publication date

1 January 2003

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9 August 2017

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9 August 2017

volume

14

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9 August 2017

issue

4

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9 August 2017

page(s)

375-382

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https://scigraph.springernature.com/pub.10.1385/ep:14:4:375

9 August 2017

exact match

0 references

cites work

A patient with MEN 2 and multiple mutations of RET in the germline

1 reference

12 December 2020

Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 cases

1 reference

12 December 2020

Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

1 reference

12 December 2020

Expression of the ret proto-oncogene in phaeochromocytoma. An in situ hybridization and northern blot study

1 reference

12 December 2020

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.

1 reference

12 December 2020

Germline mutation of RET codon 883 in two cases of de novo MEN 2B.

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12 December 2020

The phenotypes associated with ret mutations in the multiple endocrine neoplasia type 2 syndrome.

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12 December 2020

Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma.

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12 December 2020

Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study.

1 reference

12 December 2020

Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease

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12 December 2020

Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas

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12 December 2020

Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease

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12 December 2020

Duplication of 9 base pairs in the critical cysteine-rich domain of the RET proto-oncogene causes multiple endocrine neoplasia type 2A

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12 December 2020

Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene

1 reference

12 December 2020

Pheochromocytoma: inherited associations, bilaterality, and cortex preservation

1 reference

12 December 2020

Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas

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12 December 2020

Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance

1 reference

12 December 2020

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

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12 December 2020

The RET proto-oncogene in sporadic pheochromocytomas

1 reference

12 December 2020

First continuous human pheochromocytoma cell line: KNA. Biological, cytogenetic and molecular characterization of KNA cells

1 reference

12 December 2020

Pheochromocytoma in multiple endocrine neoplasia type 2: European study

1 reference

12 December 2020

A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene

1 reference

12 December 2020

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

1 reference

12 December 2020

A RET double mutation in the germline of a kindred with FMTC.

1 reference

12 December 2020

Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas

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12 December 2020

[Pheochromocytoma associated with multiple endocrine neoplasia 2A and sporadic: differential characteristics]

1 reference

12 December 2020

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

1 reference

12 December 2020

A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A

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12 December 2020

Expression analysis of RET and the GDNF/GFRalpha-1 and NTN/GFRalpha-2 ligand complexes in pheochromocytomas and paragangliomas

1 reference

12 December 2020

Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.

1 reference

12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

12 December 2020

Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. "Study Group Multiple Endocrine Neoplasia Austria (SMENA)".

1 reference

12 December 2020

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas

1 reference

12 December 2020

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

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12 December 2020

RET proto-oncogene in the development of human cancer

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12 December 2020

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas

1 reference

12 December 2020

Identifiers

DOI

10.1385/EP:14:4:375

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Dimensions Publication ID

9 August 2017

1030578981

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