(Q36121940)

12 August 2017

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title

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

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von Hippel-Lindau disease

12 August 2017

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1

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12 August 2017

Francesca Schiavi

3

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author name string

Pierantonio Conton

series ordinal

2

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12 August 2017

Beatrice Macino

series ordinal

4

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12 August 2017

Franco Mantero

series ordinal

5

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12 August 2017

language of work or name

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1 January 2005

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12 August 2017

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12 August 2017

volume

4

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12 August 2017

issue

1

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12 August 2017

page(s)

13-16

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The genetic basis of pheochromocytoma.

12 August 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS10689-004-6128-Y

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

21 January 2018

1 reference

12 December 2020

Molecular basis of the VHL hereditary cancer syndrome

1 reference

12 December 2020

Blood pressure and cardiovascular involvement in children with neurofibromatosis type1

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical review 155: Pheochromocytoma in Von Hippel-Lindau disease

1 reference

12 December 2020

Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis

1 reference

12 December 2020

Structure of the VHL-ElonginC-ElonginB complex: implications for VHL tumor suppressor function

1 reference

12 December 2020

Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

1 reference

12 December 2020

Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I

1 reference

12 December 2020

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

1 reference

12 December 2020

von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF.

1 reference

12 December 2020

The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors

1 reference

12 December 2020

von Recklinghausen's disease and pheochromocytomas

1 reference

12 December 2020

Cardiovascular disease in neurofibromatosis 1: report of the NF1 Cardiovascular Task Force

1 reference

12 December 2020

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

1 reference

12 December 2020

Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome

1 reference

12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

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12 December 2020

Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

1 reference

12 December 2020

10.1007/S10689-004-6128-Y

Identifiers

DOI

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12 August 2017

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