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1.  Treatment of rheumatoid arthritis in patients with concomitant chronic hepatitis C infection 
Hepatitis C virus (HCV) infection is present in 1.8% of the general US population and its prevalence worldwide is estimated at 2–3%. HCV infected patients with concomitant rheumatoid arthritis (RA) pose a particular challenge to the rheumatologist because of the risks of treatment with disease-modifying medications in patients with chronic liver infection. In this paper the difficulties of diagnosing RA in HCV patients and the safety of RA treatment in patients with both conditions are discussed.
doi:10.1177/1759720X11424459
PMCID: PMC3383526  PMID: 22870493
biological-response modifiers; disease-modifying antirheumatic drugs; hepatitis C; rheumatoid arthritis
2.  Spinal gout mimicking paraspinal abscess: A case report 
Gout is usually thought of as a peripheral joint disease. However, case reports are available describing gouty lesions in the spine. We report a case of a 51 year old African American woman with no previous history of gout who presented with lower back pain and fever and was found to have multiple small fluid collections in the paraspinal muscles at the L3 to L5 levels on the MRI. She was empirically treated with antibiotics, since the fluid was not accessible for drainage initially. Unsuccessful antibiotic therapy and an episode of peripheral gout during this hospitalization prompted the diagnosis of axial gout as the cause for the paraspinal lesions in this patient. CT guided aspiration of the paraspinal lesions confirmed monosodium urate (gout) crystals under polarized microscopy.
doi:10.3941/jrcr.v4i6.332
PMCID: PMC3303413  PMID: 22470736
Axial gout; spinal lesions; paraspinal abscess; uric acid
3.  A truncated T antigen expressed from an alternatively spliced BK virus early mRNA 
The Journal of General Virology  2009;90(Pt 5):1238-1245.
The early region of BK virus (BKV) is known to encode two well-characterized tumour (T) antigens, large T antigen (TAg) and small T antigen (tAg). In this study, we provide evidence of a third early BKV mRNA that codes for an additional early region product with an apparent molecular mass of 17–20 kDa. This truncated form of TAg (truncTAg) is expressed from an alternatively spliced mRNA that is derived from the excision of a second intron from the mRNA encoding TAg. The first 133 aa of truncTAg are identical to those of TAg but the additional splice results in translation from a different reading frame, adding three new amino acids before reaching a stop codon. TruncTAg is expressed in both BKV-transformed and lytically infected cells and it is found to be primarily localized to the nucleus. The function of BKV truncTAg is likely to be relevant to transformation, similar to the additional T antigens of simian virus 40, JC virus and mouse polyomavirus.
doi:10.1099/vir.0.009159-0
PMCID: PMC2887564  PMID: 19264611

Results 1-3 (3)