(Q74454015)

English

Pheochromocytoma in von hippel-lindau disease: distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2

scientific article published on 01 January 2002

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Pheochromocytoma in von hippel-lindau disease: distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

phaeochromocytoma

1 reference

based on heuristic

inferred from title

multiple endocrine neoplasia type 2

1 reference

based on heuristic

inferred from title

von Hippel-Lindau disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Christian A. Koch

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Georgios P. Chrousos

8

object named as

George P Chrousos

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

David Mauro

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

McClellan M Walther

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

W Marston Linehan

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Alexander O Vortmeyer

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Ronald Jaffe

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Karel Pacak

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Zhengping Zhuang

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Irina A Lubensky

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 January 2002

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Endocrine Pathology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

13

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

17-27

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12114747%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

https://scigraph.springernature.com/pub.10.1385/ep:13:1:17

0 references

Genetic aspects of pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of pheochromocytoma in hypertensive patients with neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple paragangliomas in neurofibromatosis: a new neuroendocrine neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hippel-Lindau disease: MR imaging

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia, type 2b

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differences between sporadic pheochromocytoma and pheochromocytoma in multiple endocrine neoplasia, type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral adrenal medullary hyperplasia: a clinicopathological entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathology of multiple endocrine neoplasias 2A and 2B: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A patient with neurofibromatosis type 1 and watery diarrhoea syndrome due to a VIP-producing adrenal phaeochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of von Recklinghausen's disease with bilateral pheochromocytoma-malignant peripheral nerve sheath tumors of the adrenal and gastrointestinal autonomic nerve tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia. Type IIa.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial pheochromocytoma, hypercalcemia, and von Hippel-Lindau disease. A ten year study of a large family

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparative study of 14 cases of familial and nonfamilial pheochromocytomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis, localization, and management of pheochromocytoma. Pitfalls and follow-up in 41 patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenal medullary disease in multiple endocrine neoplasia, type 2: pheochromocytoma and its precursors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[112 cases of sporadic and genetically determined pheochromocytoma: a comparative pathologic study]

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial pheochromocytoma associated with von Recklinghausen's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: the precursor of bilateral pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenal medullary hyperplasia. A morphometric analysis in patients with familial medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis, von Recklinghausen's disease of the nervous system; analysis of the total pathologic picture

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Management of hereditary pheochromocytoma in von Hippel-Lindau kindreds with partial adrenalectomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Von Hippel-Lindau disease: clinical and pathological manifestations in nine families with 50 affected members

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

von Recklinghausen's disease and pheochromocytomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the RET protooncogene in sporadic pheochromocytomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CT screening of the abdomen in von Hippel-Lindau disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Von Recklinghausen's disease (neurofibromatosis) associated with malignant pheochromocytoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Silent adrenal nodules in von Hippel-Lindau disease suggest pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenal pheochromocytoma: a clinicopathologic review of 60 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathology and molecular genetics of multiple cysts and microcystic (serous) adenomas of the pancreas in von Hippel-Lindau patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survivin: a novel neuroendocrine marker for pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis: past, present, and future

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concomitant occurrence of an adrenal ganglioneuroma and a contralateral pheochromocytoma in a patient with von Recklinghausen's neurofibromatosis. An immunocytochemical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12114747

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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