نتایج جستجو برای: hyper immunoglobulin e syndrome

تعداد نتایج: 1675937  

2003
Per Svensson

The paper discusses architectural options for providing Dominant Battlespace Awareness (DBA) for Archipelagic Anti-Submarine Warfare (AASW) in the Baltic Sea, against experience from submarine intelligence data analysis and fusion research during the recent historical episode which involved recurrent submarine intrusions into Swedish

Journal: :Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2016
Türkan Patıroğlu Himmet Haluk Akar Mehmet Sait Doğan Kazım Üzüm

Dedicator of cytokinesis 8 protein (DOCK8) deficiency is an autosomal recessive, inherited form of hyper-immunoglobulin E (hyper-IgE) syndrome, characterized by persistent cutaneous viral infections, elevated IgE, eosinophilia, and allergic manifestations. The case of a 10-year-old boy who presented with giant aortic aneurysm between the aortic root and iliac bifurcation is described in the pre...

2014
Martin Sikora Meredith L. Carpenter Andres Moreno-Estrada Brenna M. Henn Peter A. Underhill Federico Sánchez-Quinto Ilenia Zara Maristella Pitzalis Carlo Sidore Fabio Busonero Andrea Maschio Andrea Angius Chris Jones Javier Mendoza-Revilla Georgi Nekhrizov Diana Dimitrova Nikola Theodossiev Timothy T. Harkins Andreas Keller Frank Maixner Albert Zink Goncalo Abecasis Serena Sanna Francesco Cucca Carlos D. Bustamante

Genome sequencing of the 5,300-year-old mummy of the Tyrolean Iceman, found in 1991 on a glacier near the border of Italy and Austria, has yielded new insights into his origin and relationship to modern European populations. A key finding of that study was an apparent recent common ancestry with individuals from Sardinia, based largely on the Y chromosome haplogroup and common autosomal SNP var...

2012
Katarzyna Jończyk-Potoczna Aleksandra Szczawińska-Popłonyk Małgorzata Warzywoda Anna Bręborowicz Bogdan Pawlak

BACKGROUND Hyperimmunoglobulinemia E syndrome (hyper-IgE syndrome, Job syndrome, HIES) is a complex immune deficiency with multiorgan clinical manifestations and diverse genetic background. The clinical triad of symptoms observed in approximately 75% of patients with HIES includes: recurrent abscesses of staphylococcal etiology, recurrent respiratory infections and elevated immunoglobulin E in ...

Journal: :caspian journal of internal medicine 0
javad ghaffari saeed abedian- kenari maryam ghasemi farzad gohardehi

background: hyper ige syndrome (hies) is a rare primary immune deficiency, described as job`s syndrome characterized by increased serum levels of ige, eczema, recurrent cutaneous and pulmonary infections. in this paper, we presented a case of hyper ige syndrome.case presentation: a 16-year-old iranian boy presented with a one year history of skin lesions in knees and elbows was diagnosed of pso...

2017
Amrita Dosanjh

Patients with autosomal-dominant (AD) hyper immunoglobulin E (IgE) syndrome (HIES) or Job syndrome develop frequent dermatologic and pulmonary infections. As patients have an extreme elevation of IgE levels, this database analysis study sought to study the association between AD HIES, Job syndrome, and anaphylaxis. HIES is a heterogeneous group of immune disorders characterized by extremely ele...

2010
Lixin Xie Xiaoxiang Hu Yang Li Weihua Zhang Liang'an Chen

Hyper-immunoglobulin E syndromes (HIES) including compound primary immunodeficiency and nonimmunological abnormalities are characterized by extremely high serum IgE levels, eosinophilia, eczema, susceptibility to infections, distinctive facial appearance, retention of deciduous teeth, cyst-forming pneumonias, and skeletal abnormalities. Itis reported that some cases of familial HIES are relativ...

Journal: :Clinical genetics 2014
J Diamond

Aicardi-Goutières Syndrome is caused by IFIH1 mutations Oda et al.(2014) The American Journal of Human Genetics 95(1): 121-125. Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling Rice et al.(2014) Nature Genetics 46(5): 503-510.

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