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

JCH van der Hilst, EJ Bodar, KS Barron, J Frenkel… - Medicine, 2008 - journals.lww.com
The hyperimmunoglobulinemia D and periodic fever syndrome (HIDS), one of the
autoinflammatory syndromes, is caused by mutations in the gene coding for mevalonate …

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

W Ammouri, L Cuisset, S Rouaghe, MO Rolland… - …, 2007 - academic.oup.com
Objective. The hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) was
originally defined by the presence of a high serum level of immunoglobulin D associated …

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

L Cuisset, JPH Drenth, A Simon, MF Vincent… - European Journal of …, 2001 - nature.com
Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) is an autosomal
recessive inflammatory disorder characterised by recurrent episode of fever associated with …

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

A Simon, L Cuisset, MF Vincent… - Annals of internal …, 2001 - acpjournals.org
Background: The hyper-IgD and periodic fever syndrome (HIDS) is characterized by
recurrent attacks of fever, abdominal distress, and arthralgia and is caused by mevalonate …

Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D

J Frenkel, SM Houten, HR Waterham… - …, 2001 - academic.oup.com
Objectives. The hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) was
found recently to be caused by a deficiency of mevalonate kinase (MK). The aim of this study …

Treatment with anakinra in the hyperimmunoglobulinemia D/periodic fever syndrome

D Rigante, V Ansuini, B Bertoni, AL Pugliese… - Rheumatology …, 2006 - Springer
Hyperimmunoglobulinemia D/periodic fever syndrome is caused by recessively inherited
mutations in the mevalonate kinase gene and is characterized by persistently high …

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

K Takada, I Aksentijevich, V Mahadevan… - … : Official Journal of …, 2003 - Wiley Online Library
Objective The hyperimmunoglobulinemia D and periodic fever syndrome (HIDS; MIM
260920) is caused by recessive mutations in the mevalonate kinase gene (MVK), which …

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

A D'Osualdo, P Picco, F Caroli, M Gattorno… - European journal of …, 2005 - nature.com
Autosomal recessive autoinflammatory disorder caused by mutations of the mevalonate
kinase gene (MVK), leading to mild, incomplete MK enzyme deficiency (MKD), has been …

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

A Simon, E Drewe, JWM Van Der Meer… - Clinical …, 2004 - Wiley Online Library
Hyperimmunoglobulinemia D (hyper‐IgD) and periodic fever syndrome, a hereditary
autoinflammatory syndrome, is characterized by lifelong recurrent episodes of fever and …

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

SM Houten, W Kuis, M Duran, TJ De Koning… - Nature …, 1999 - nature.com
Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS; MIM 260920) is an
autosomal recessive disorder characterized by recurrent episodes of fever associated with …