Results 101 to 110 of about 2,216 (148)

Case Report: Early-onset mevalonic aciduria in neonates with inflammatory marker elevated. [PDF]

Front Immunol
Xue S, Shi W, He X, Hao L.
europepmc   +1 more source

Genetic and epidemiological patterns of primary immunodeficiency diseases in Eastern Iranian patients. [PDF]

Sci Rep
Salehi M, Ahanchian H, Karimiani EG, Aelami MH, Moazzen N, Neshati Z, Pasdar A.   +6 more
europepmc   +1 more source

Zespół hiper-IgD (ang. hyper-IgD syndrome, HIDS). [W : zespoły autozapalne]

, 2018
openaire   +1 more source

Hyper-IgD Syndrome and pregnancy

European Journal of Obstetrics, Gynecology and Reproductive Biology, 1996
In this report two cases of the coincidence of hyperimmunoglobulinemia D syndrome (HIDS) and pregnancy are described. HIDS is not associated with complications in pregnancy or disturbance in fetal outcome; the frequency of attacks diminishes during pregnancy; HIDS probably inherits via an autosomal recessive trait and is not transmitted to children of ...
J A de Hullu, J A de Hullu
exaly   +5 more sources

Some of the next articles are maybe not open access.

Related searches:

Das Hyper-IgD-Syndrom (The hyper-IgD-syndrome)

Zeitschrift f�r Rheumatologie, 1997
We report on a 6-year-old Romanian girl with recently diagnosed hyper-IgD-syndrome. The leading symptom of this rare disease are periodic pyrexia, joint involvements (arthralgias/arthritis) and swollen lymph nodes. A permanent increase of alpha 1-acid glycoprotein fucosylation indicates persisting inflammation.
J. Suschke, J.-U. Walther
openaire   +2 more sources

A patient with hyper-IgD syndrome in Antalya, Turkey

Clinical Rheumatology, 2004
Hyper-IgD syndrome is a periodic fever syndrome that presents with recurrent episodes of high fever accompanied by lymphadenopathy, abdominal distress, arthralgias or arthritis, headache and skin lesions. The diagnosis is based on clinical grounds and elevated serum IgD levels (>100 U/ml), but requires a high index of suspicion, and a mevalonate kinase
Erkan Çoban, Mustafa Ender Terzioğlu
exaly   +3 more sources

Hyper-IGD syndrome: A new case treated with colchicine

Clinical Rheumatology, 1988
We report a new case of hyper-IgD syndrome, a recently described disease characterized by recurrent episodes of fever with headache, bilateral cervical lymphadenopathy and, more rarely, abdominal pain and diarrhoea. Polyclonal increase of serum IgD is the most important laboratory finding.
Paolo Lazzarin, Silvano Todesco, P F Gambari   +2 more
exaly   +3 more sources

Crescentic glomerulonephritis in hyper IgD syndrome

Pediatric Nephrology, 1999
The hyperimmunoglobulinemia D syndrome (HIDS) is a well-defined entity resembling familial Mediterranean fever. HIDS is a systemic inflammatory disease associated with stimulation of T-cell-mediated immunity. These patients are at low risk for amyloidosis and are not known to develop nephropathy.
M, Tsimaratos, I, Koné-Paut, L, Daniel, M C, Gubler, B, Dussol, G, Picon   +5 more
openaire   +2 more sources

Un cas de syndrome hyper-IgD

Revue Francophone Des Laboratoires, 2019
Resume Les fievres recurrentes de l’enfant sont de diagnostic etiologique difficile, car concernent des anomalies metaboliques ou genetiques souvent non encore connues. Elles sont associees a des maladies dont les mecanismes physiopathologiques, et donc les marqueurs biologiques, commencent a etre elucides.
Marie-Nathalie Kolopp-Sarda
exaly   +2 more sources

Treatment of adult hyper-IgD syndrome with canakinumab

The Journal of Allergy and Clinical Immunology: In Practice, 2015
Hyper-IgD and periodic fever syndrome (HIDS) is a rare, autosomal-recessive autoinflammatory disease characterized by lifelong recurrent episodes of systemic inflammation. HIDS frequently presents in infancy with intermittent fevers lasting from 4 to 7 days, recurring every 4 to 6 weeks.
Casey D, Curtis, Charity C, Fox
openaire   +2 more sources