(Q38014788)

27 August 2017

Hereditary pheochromocytoma and paraganglioma (English)

1 reference

27 August 2017

1 reference

Peter J Mazzaglia

1

1 reference

27 August 2017

30 May 2012

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Journal of Surgical Oncology

27 August 2017

1 reference

27 August 2017

106

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27 August 2017

5

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27 August 2017

580-585

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Pheochromocytoma in Italy: a multicentric retrospective study

27 August 2017

1 reference

Genetic basis of phaeochromocytoma and paraganglioma

21 January 2018

1 reference

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

21 January 2018

1 reference

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

21 January 2018

1 reference

SDHA is a tumor suppressor gene causing paraganglioma

21 January 2018

1 reference

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

21 January 2018

1 reference

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

21 January 2018

1 reference

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

21 January 2018

1 reference

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

21 January 2018

1 reference

Pheochromocytoma: the expanding genetic differential diagnosis

21 January 2018

1 reference

Germ-line mutations in nonsyndromic pheochromocytoma

21 January 2018

1 reference

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

21 January 2018

1 reference

The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.

21 January 2018

1 reference

Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor

21 January 2018

1 reference

Distribution of 13 truncating mutations in the neurofibromatosis 1 gene

21 January 2018

1 reference

Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.

21 January 2018

1 reference

Genetic testing in pheochromocytoma or functional paraganglioma

21 January 2018

1 reference

Genetic testing for pheochromocytoma

21 January 2018

1 reference

Phaeochromocytoma, new genes and screening strategies.

21 January 2018

1 reference

Germline SDHB mutations and familial renal cell carcinoma.

21 January 2018

1 reference

Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD.

21 January 2018

1 reference

Loss of SDHB and NF1 genes in a malignant phyllodes tumor of the breast as detected by oligo-array comparative genomic hybridization

21 January 2018

1 reference

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

21 January 2018

1 reference

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

21 January 2018

1 reference

Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

21 January 2018

1 reference

Genetic screening for pheochromocytoma: should SDHC gene analysis be included?

21 January 2018

1 reference

Plasma metanephrines: a novel and cost-effective test for pheochromocytoma

21 January 2018

1 reference

A systematic review of the literature examining the diagnostic efficacy of measurement of fractionated plasma free metanephrines in the biochemical diagnosis of pheochromocytoma

21 January 2018

1 reference

A comparison of biochemical tests for pheochromocytoma: measurement of fractionated plasma metanephrines compared with the combination of 24-hour urinary metanephrines and catecholamines

21 January 2018

1 reference

Biochemical diagnosis of pheochromocytoma: which test is best?

21 January 2018

1 reference

Clinical review 164: The laboratory diagnosis of adrenal pheochromocytoma: the Mayo Clinic experience

21 January 2018

1 reference

Fluorine-18 DOPA PET imaging of paraganglioma syndrome

21 January 2018

1 reference

Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients

21 January 2018

1 reference

21 January 2018

1 reference

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

21 January 2018

1 reference

Pheochromocytoma: recommendations for clinical practice from the First International Symposium. October 2005.

21 January 2018

1 reference

Genetic testing in pheochromocytoma: increasing importance for clinical decision making

21 January 2018

1 reference

Succinate Dehydrogenase B Gene Mutations Predict Survival in Patients with Malignant Pheochromocytomas or Paragangliomas

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/JSO.23157

1 reference

27 August 2017

1 reference

PubMed ID

22648936