(Q34972749)

5 August 2017

1 reference

title

Etiopathogenesis and clinical presentation of carotid body tumors (English)

1 reference

5 August 2017

Bora E Baysal

1

1 reference

PubMed ID

12384970

5 August 2017

Eugene N Myers

series ordinal

2

1 reference

5 August 2017

1 November 2002

1 reference

Microscopy Research and Technique

5 August 2017

1 reference

5 August 2017

59

1 reference

5 August 2017

3

1 reference

5 August 2017

256-261

1 reference

Carotid body tumor associated with hyperparathyroidism

5 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Germline SDHD mutation in familial phaeochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Genetics of familial paragangliomas: past, present, and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Molecular pathogenesis in sporadic head and neck paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Gastric stromal sarcoma, pulmonary chondroma, and extra-adrenal paraganglioma (Carney Triad): natural history, adrenocortical component, and possible familial occurrence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Multiple paragangliomas in neurofibromatosis: a new neuroendocrine neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

The carotid body in animals at high altitude

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Genetic testing for cancer predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Human Cancer Syndromes: Clues to the Origin and Nature of Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Familial carotid body tumors: case report and epidemiologic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Regulation of oxygen sensing in peripheral arterial chemoreceptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Genetic analysis in the diagnosis of familial paragangliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Cellular mechanisms of oxygen sensing at the carotid body: heme proteins and ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Bilateral carotid body paraganglioma and central alveolar hypoventilation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10200

21 January 2018

Identifiers

DOI

10.1002/JEMT.10200

1 reference

5 August 2017

1 reference

PubMed ID

12384970