(Q37738109)

22 August 2017

1 reference

title

Hyperimmunoglobulin D syndrome in childhood (English)

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22 August 2017

author name string

Jeroen C H van der Hilst

series ordinal

1

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22 August 2017

Joost Frenkel

series ordinal

2

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22 August 2017

publication date

1 April 2010

1 reference

Current Rheumatology Reports

22 August 2017

published in

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22 August 2017

volume

12

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22 August 2017

issue

2

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22 August 2017

page(s)

101-107

1 reference

https://scigraph.springernature.com/pub.10.1007/s11926-010-0086-1

22 August 2017

exact match

0 references

cites work

Hyperimmunoglobulinaemia D and periodic fever: a new syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11926-010-0086-1

Biochemical and genetic aspects of mevalonate kinase and its deficiency

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11926-010-0086-1

First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome

21 January 2018

1 reference

12 December 2020

Defective apoptosis of peripheral-blood lymphocytes in hyper-IgD and periodic fever syndrome.

1 reference

12 December 2020

The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome

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12 December 2020

Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations

1 reference

12 December 2020

Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The course of life of survivors of childhood cancer.

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12 December 2020

A role for geranylgeranylation in interleukin-1beta secretion

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary periodic fever

1 reference

12 December 2020

Effect of etanercept and anakinra on inflammatory attacks in the hyper-IgD syndrome: introducing a vaccination provocation model.

1 reference

12 December 2020

Diagnostics and therapeutic insights in a severe case of mevalonate kinase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Young adult patients with a history of pediatric disease: impact on course of life and transition into adulthood.

1 reference

12 December 2020

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

1 reference

12 December 2020

Simvastatin treatment for inflammatory attacks of the hyperimmunoglobulinemia D and periodic fever syndrome

1 reference

12 December 2020

Limited efficacy of thalidomide in the treatment of febrile attacks of the hyper-IgD and periodic fever syndrome: a randomized, double-blind, placebo-controlled trial

1 reference

12 December 2020

HMG-CoA reductase inhibition induces IL-1beta release through Rac1/PI3K/PKB-dependent caspase-1 activation

1 reference

12 December 2020

Statin synergizes with LPS to induce IL-1beta release by THP-1 cells through activation of caspase-1.

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12 December 2020

Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes

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12 December 2020

An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist

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12 December 2020

Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndrome

1 reference

12 December 2020

AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases

1 reference

12 December 2020

Hyperimmunoglobulinemia D and periodic fever syndrome. The clinical spectrum in a series of 50 patients. International Hyper-IgD Study Group

1 reference

12 December 2020

Autoinflammatory gene mutations in Behçet's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Specific increase in caspase-1 activity and secretion of IL-1 family cytokines: a putative link between mevalonate kinase deficiency and inflammation

1 reference

12 December 2020

Hereditary periodic fever and reactive amyloidosis.

1 reference

12 December 2020

Lives in a Balance: Perceived Family Functioning and the Psychosocial Adjustment of Adolescent Cancer Survivors

1 reference

12 December 2020

Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome.

1 reference

12 December 2020

Nummular keratopathy in a patient with Hyper-IgD Syndrome

1 reference

12 December 2020

Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)

1 reference

12 December 2020

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

1 reference

12 December 2020

Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D.

1 reference

12 December 2020

Treatment with anakinra in the hyperimmunoglobulinemia D/periodic fever syndrome

1 reference

12 December 2020

10.1007/S11926-010-0086-1

Identifiers

DOI

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22 August 2017

1 reference