(Q40307592)

English

Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children

scientific article published on 30 October 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

periodic fever syndrome

1 reference

based on heuristic

inferred from title

hyper-IgD syndrome

1 reference

based on heuristic

inferred from title

author name string

E Lainka

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

U Neudorf

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

P Lohse

3

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

C Timmann

4

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

M Bielak

5

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

S Stojanov

6

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

K Huss

7

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

R von Kries

8

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

T Niehues

9

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

publication date

30 October 2011

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Rheumatology International

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

32

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

3253-3260

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

https://scigraph.springernature.com/pub.10.1007/s00296-011-2180-8

0 references

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Hyperimmunoglobulinemia D and periodic fever syndrome in children. Review on therapy with biological drugs and case report

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Mevalonate kinase deficiency: Evidence for a phenotypic continuum.

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the Netherlands

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Autoinflammatory conditions: when to suspect? How to treat?

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

B cell cytopenia in two brothers with hyper-IgD and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

A founder effect in the hyperimmunoglobulinemia D and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Autoinflammatory syndromes: diagnosis and management

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Periodic fever in children with hyperimmunoglobulinemia D and mevalonate kinase mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Long-term follow-up, clinical features, and quality of life in a series of 103 patients with hyperimmunoglobulinemia D syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference.

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Hyperimmunoglobulin D syndrome in childhood

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

A clinical criterion to exclude the hyperimmunoglobulin D syndrome (mild mevalonate kinase deficiency) in patients with recurrent fever

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Familial autoinflammatory diseases: genetics, pathogenesis and treatment

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Dysregulation of innate immunity: hereditary periodic fever syndromes.

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Web resources for rare auto-inflammatory diseases: towards a common patient registry

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Translational research network and patient registry for auto-inflammatory diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2180-8

21 January 2018

Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the

1 reference

https://pubmed.ncbi.nlm.nih.gov/22038276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fevers, genes, and innate immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/22038276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoinflammatory syndromes behind the scenes of recurrent fevers in children.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22038276

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00296-011-2180-8

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

ResearchGate publication ID

0 references

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