Results 71 to 80 of about 2,267,031 (171)
Hyper-IgD syndrome and other hereditary periodic fever syndromes
, 2004 Hereditary periodic fever syndromes are a group of systemic disorders characterized by recurrent attacks of systemic inflammation (autoinflammation) without infectious or autoimmune cause.
BOCCAFOGLI, Arrigo +2 more
core
Clinical manifestation of autosomal dominant hyper-IgE syndrome with associated autism
Autosomal dominant hyper-IgE syndrome (AD-HIES) is a rare inborn error of immunity that affects multiple organs and presents a wide array of clinical features.
Adrianna Muciek +2 more
core +1 more source
The Turkish Journal of Pediatrics, 2012 The hyperimmunoglobulinemia D syndrome (HIDS), so-called mevalonate kinase deficiency, is caused by recessive mutations in the gene encoding mevalonate kinase enzyme.
Pınar Gençpınar +4 more
doaj
Linear and whorled nevoid hypermelanosis with hyper IgE syndrome
, 2015 Introduction . Linear and whorled nevoid hypermelanosis (LWNH) is a disorder of pigmentation characterized by macular hyperpigmentation following the Blaschko lines. Only 50 cases of LWNH have been described so far.
Joanna Narbutt +4 more
core +1 more source
Hyperimmunoglobulinemia D and periodic fever syndrome : the clinical spectrum in a series of 50 patients : the International Hyper-IgD Study Group [PDF]
, 1994 Contains fulltext : 4781.pdf (Publisher’s version ) (Open Access)The International Hyper-IgD Study ...
Haagsma, C.J. +2 more
core +1 more source
Interleukin 1 blockade withcanakinumab for Hyper IGD syndrome (HIDS) [PDF]
Pediatr Rheumatol Online J, 2015 Brunnner J +4 more
europepmc +1 more source