✦ LIBER ✦

Mutations of the hemophagocytic lymphohistiocytosis–associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis

✍ Scribed by Melissa M. Hazen; Amy L. Woodward; Inga Hofmann; Barbara A. Degar; Alexei Grom; Alexandra H. Filipovich; Bryce A. Binstadt

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 88 KB
Volume: 58
Category: Article
ISSN: 0004-3591
DOI: 10.1002/art.23199

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation screening of the macrophage mig

Mutation screening of the macrophage migration inhibitory factor gene: Positive association of a functional polymorphism of macrophage migration inhibitory factor with juvenile idiopathic arthritis

✍ Rachelle Donn; Zaynab Alourfi; Fabrizio De Benedetti; Cristina Meazza; Eleftheri 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 93 KB 👁 2 views

Increased interleukin-18 expression in b

Increased interleukin-18 expression in bone marrow of a patient with systemic juvenile idiopathic arthritis and unrecognized macrophage-activation syndrome

✍ Nobuaki Maeno; Syuji Takei; Hiroyuki Imanaka; Kimie Yamamoto; Kazumi Kuriwaki; Y 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 245 KB 👁 1 views

## Abstract The aberrant induction of proinflammatory cytokines is considered to be crucial in the pathogenesis of systemic juvenile idiopathic arthritis and adult‐onset Still's disease. Interleukin‐18 (IL‐18) in particular has been reported to be a candidate for the key cytokine in both diseases;

Higher frequency of allele 2 of the inte

Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritis

✍ Jiří Vencovský; Kateřina Jarošová; šárka Růžičková; Dana Němcová; Jaroslava Nied 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 59 KB 👁 2 views

The −174G allele of the interleukin-6 ge

The −174G allele of the interleukin-6 gene confers susceptibility to systemic arthritis in children: A multicenter study using simplex and multiplex juvenile idiopathic arthritis families

✍ Emma M. Ogilvie; Mark S. Fife; Susan D. Thompson; Natalie Twine; Monica Tsoras; 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 66 KB 👁 1 views

Two novel missense mutations of the OCTN

Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency

✍ E. Mayatepek; J. Nezu; I. Tamai; A. Oku; M. Katsura; M. Shimane; A. Tsuji 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 20 KB 👁 1 views

Primary systemic carnitine deficiency (SCD) is an autosomal recessive disorder of fatty acid oxidation caused by defective cellular carnitine transport. The disease is characterized by metabolic derangement simulating Reye´s syndrome, hypoglcaemia, progressive cardiomyopathy and skeletal myopathy. R

Assessment of inflammatory response in a

Assessment of inflammatory response in a study of uveitis associated with juvenile idiopathic arthritis: comment on the article by Smith et al

✍ Liu, David T. L. ;Chan, Alice Y. K. 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB 👁 2 views