An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis (Q36477902)

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English	An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis	scientific article

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scholarly article

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14 August 2017

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis (English)

1 reference

Europe PubMed Central

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14 August 2017

immunohistochemistry

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based on heuristic

inferred from title

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based on heuristic

inferred from title

Jérôme Bertherat

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Jérôme Bertherat

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Patrick J Pollard

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Patrick J Pollard

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Laurence Amar

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Judith Favier

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Eamonn R Maher

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Massimo Mannelli

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Massimo Mannelli

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Anne-Paule Gimenez-Roqueplo

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Anne-Paule Gimenez-Roqueplo

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Aurel Perren

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13

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Karel Pacak

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Wouter W de Herder

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Wouter W de Herder

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Jacques W M Lenders

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Jacques W M Lenders

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Ronald de Krijger

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Ronald R de Krijger

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Winand N M Dinjens

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Winand N M Dinjens

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Esther Korpershoek

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Esther Korpershoek

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José Gaal

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Francien H van Nederveen

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Francien H van Nederveen

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Hein F B M Sleddens

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Hein F B M Sleddens

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Hilde Dannenberg

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Hilde Dannenberg

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Albert A Verhofstad

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Albert A Verhofstad

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author name string

Rogier A Oldenburg

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Elly M C A de Bruyn

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Pieter Derkx

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Julie Rivière

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Bart-Jeroen Petri

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Paul Komminoth

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Wim C J Hop

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Jean-Pierre Bayley

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Stephan Niemann

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Adriaan P de Bruïne

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Frédérique Tissier

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Tchao Méatchi

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Cécile Badoual

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Despoina Alataki

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Eric Van Marck

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Francesco Ferrau

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Jerney François

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Mark-Paul F M Vrancken Peeters

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Anne van Linge

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publication date

1 July 2009

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14 August 2017

Lancet Oncology Commission

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10

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8

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764-771

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Europe PubMed Central

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14 August 2017

Germline SDHB mutations and familial renal cell carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Cells silenced for SDHB expression display characteristic features of the tumor phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Pheochromocytoma: an update on genetics and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Mitochondrial tumour suppressors: a genetic and biochemical update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Phaeochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

30 September 2017

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Phaeochromocytoma, new genes and screening strategies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Genetic testing in pheochromocytoma or functional paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Immunological approaches to the characterization and diagnosis of mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

G12S and H50R variations are polymorphisms in the SDHD gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Succinate:quinone oxidoreductases: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4718191

21 September 2018

Somatic SDHB mutation in an extraadrenal pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19576851

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of germline succinate dehydrogenase mutations in sporadic cervical paragangliomas in northern Spain: mitochondrial succinate dehydrogenase structure-function relationships and clinical-pathological correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19576851

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/19576851

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S1470-2045(09)70164-0

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

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