Search Results - "Aghighi Y."
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Association of tumour necrosis factor-alpha G/A -238 and G/A -308 single nucleotide polymorphisms with juvenile idiopathic arthritis
Published in International journal of immunogenetics (01-12-2016)“…Summary Juvenile idiopathic arthritis (JIA) is a heterogeneous autoimmune disorder of unknown origin. As proinflammatory cytokines are known to contribute…”
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Interleukin-4 single nucleotide polymorphisms in juvenile systemic lupus erythematosus
Published in International journal of immunogenetics (01-12-2014)“…Summary Juvenile systemic lupus erythematosus (JSLE) is a chronic, recurrent multisystem inflammatory disease, caused by a combination of environmental events…”
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Association of interleukin-2 and interferon-γ single nucleotide polymorphisms with Juvenile systemic lupus erythematosus
Published in Allergologia et immunopathologia (01-09-2016)“…Juvenile systemic lupus erythematosus (JSLE) is a severe and chronic autoimmune disease of unknown origin. Inflammatory cytokines can play a pivotal role in…”
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Interleukin 10 and transforming growth factor beta 1 gene polymorphisms in juvenile idiopathic arthritis
Published in Bratislavské lékarské listy (2016)“…The aim of this study is to identify the associations between interleukin 10 (IL-10) and transforming growth factor beta 1 (TGF-β1) gene polymorphisms and…”
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Juvenile rheumatoid arthritis in children with Ebstein Barr virus infection
Published in Pakistan journal of biological sciences (15-10-2007)“…Juvenile Rheumatoid Arthritis (JRA) is a disease of unknown etiology. A total of 50 patients with JRA who were hospitalized in the Pediatrics Rheumatology Ward…”
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Relationship between eosinophilia coronary artery lesions in Kawasaki disease: a survey in Imam Khomeini Hospital
Published in Majallah-i Danishkadah-'i Pizishki (01-03-2008)“…Background: Kawasaki disease (KD) is an acute vasculitis in children. Eosinophilia, a reflection of the host's immune response that can cause tissue damage,…”
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Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene
Published in Acta dermato-venereologica (01-01-2017)Get full text
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PReS-FINAL-2083: The rate of malignancy in iranian children with joint manifestations
Published in Pediatric rheumatology online journal (05-12-2013)Get full text
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Fibrodysplasia Ossificans Progressive Two Forms of a Disease
Published in Majallah-i Dānishgāh-i ʻUlūm-i Pizishkī̄-i Bābul (01-04-2010)“…BACKGROUND AND OBJECTIVE: Fibrodysplasia ossificans progressive (FOP) or myositis ossificans progressiva is a rare hereditary connective tissue disorder…”
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Multiple Ganglion Cysts in a 21 Months Old Child
Published in Bihdād (01-10-2012)“…Ganglion cyst or synovial cysts are the most common benign tumors in the hand that arise from the synovium, tendon sheaths or tendons. The most common sites…”
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WILSON'S DISEASE IN CHILDREN, REPORT OF 25 CASES
Published in Acta medica Iranica (01-12-1984)“…We conducted a retrospective study of 25 cases (15 boys and 12 girls) of Wilson's disease(Hepatolenticular degeneration)spanning a period of 8 years. Age at…”
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WILSON'S DISEASE IN CHILDREN, REPORT OF 25 CASES
Published in Acta medica Iranica (01-05-1984)“…We conducted a retrospective study of 25 cases (15 boys and 12 girls) of Wilson's disease(Hepatolenticular degeneration)spanning a period of 8 years. Age at…”
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