(Q33430491)

26 July 2017

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients (English)

1 reference

26 July 2017

1 reference

9

Peter Devilee

0 references

author name string

Jean-Pierre Bayley

1

1 reference

26 July 2017

Anneliese E M Grimbergen

2

1 reference

26 July 2017

Patrick A van Bunderen

3

1 reference

26 July 2017

Michiel van der Wielen

4

1 reference

26 July 2017

Henricus P Kunst

5

1 reference

26 July 2017

Jacques W Lenders

6

1 reference

26 July 2017

Jeroen C Jansen

7

1 reference

26 July 2017

Robin P F Dullaart

8

1 reference

26 July 2017

Eleonora P Corssmit

10

1 reference

26 July 2017

Annette H Vriends

11

1 reference

26 July 2017

Monique Losekoot

12

1 reference

26 July 2017

Marjan M Weiss

13

1 reference

26 July 2017

15 April 2009

1 reference

26 July 2017

1 reference

26 July 2017

10

1 reference

26 July 2017

34

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-34

26 July 2017

0 references

cites work

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Paraganglioma after maternal transmission of a succinate dehydrogenase gene mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Mitochondrial tumour suppressors: a genetic and biochemical update

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Germ-line mutations in nonsyndromic pheochromocytoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2670821

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

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/10.1186%2F1471-2350-10-34

Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Molecular characterisation of a common SDHB deletion in paraganglioma patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Systematic screening and treatment evaluation of hereditary neck paragangliomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-34

Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19368708

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19368708

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular characterization of a pediatric pheochromocytoma with suspected bilateral disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19368708

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-10-34

1 reference

26 July 2017

1 reference

26 July 2017

1 reference