Letter to the Editor
- THE INDEX OF MICROCIRCULATORY RESISTANCE BUT NOT CORONARY COLLATERAL SUPPLY IS ASSOCIATED WITH MICROVASCULAR OBSTRUCTION REVEALED BY CONTRAST ENHANCED MAGNETIC RESONANCE IMAGING. // Heart;Jul2008 Supp, Vol. 94, pA81
An abstract for the article "The Index of Microcirculatory Resistance but not Coronary Collateral Supply is associated with Microvascular Obstruction revealed by Contrast Enhanced Magnetic Resonance Imaging," by C. Berry, A. Davie, and S.D. Robb is presented.
- Antiphospholipid antibody syndrome in a patient with neurosarcoidosis. Satti, S.D.; Bartholomew, J.; Gordon, S.M.; Longworth, D.L.; Ada, K.A.l. // Vascular Medicine;1999, Vol. 4 Issue 1, p37
The case of a 56-year-old woman who developed neurosarcoidosis and was discovered to have inferior vena cava and lower extremity thromboses is described. She was found to have anticardiolipin antibodies. This newly described association of antiphospholipid antibody syndrome with sarcoidosis is...
- Outcome of patients with anticardiolipin antibodies: a 10 year follow-up of 52 patients. Shah, N.M.; Khamashta, M.A.; Atsumi, T.; Hughes, G.R.V. // Lupus;1998, Vol. 7 Issue 1, p3
We report a 10-year follow-up on 52 patients with raised levels of anticardiolipin antibodies (aCL) who were first seen at our tertiary referral centre in 1986. The clinical and serological features of these 52 patients are described. Thirty-one patients had the antiphospholipid syndrome (APS)...
- Multiple sclerosis-like picture in association with Hughes syndrome. Siam, A.M.; Hammoudeh, M.; Khanjar, I. // Lupus;1998, Vol. 7 Issue 5, p367
Presents a case report of a patient with hughes syndrome, an antiphospholipid antibody syndrome. Medical history of the patient; Clinical features of hughes syndrome; Physiological changes associated with the syndrome.
- The Antiphospholipid Syndrome and ‘Multiple Sclerosis’. Hughes, G.R.V. // Lupus;1999, Vol. 8 Issue 2, p89
Editorial. Introduces several studies on multiple sclerosis in the clinical spectrum covered by antiphospholipid syndrome.
- Anti-ï¿½2-glycoprotein I autoantibodies require an antigen density threshold, consistent with divalent binding. Reddel, SW; Wang, YX; Krilis, SA // Lupus;2003, Vol. 12 Issue 1, p37
Autoantibodies binding ï¿½[sub 2]-glycoprotein I (B2GPI) are an important finding in the antiphospholipid syndrome. While antibodies from mice or rabbits immunized with B2GPI readily bind B2GPI coated on a polystyrene microwell plate, anti-B2GPI autoantibodies only do so when using a modified...
- Outcome of primary antiphospholipid syndrome in childhood. Gattorno, M.; Falcini, F.; Ravelli, A.; Zulian, F.; Buoncompagni, A.; Martini, G.; Resti, M.; Picco, P.; Martini, A. // Lupus;2003, Vol. 12 Issue 6, p449
The objective of this paper is to investigate the long-term outcome of primary antiphospholipid syndrome (APS) in the paediatric age. The features of unselected patients with primary APS who had disease onset before the age of 16 years were retrospectively analysed in three Italian referral...
- Superficial thrombophlebitis of the chest wall associated with anticardiolipin antibodies: antiphospholipid syndrome or Mondor's disease? Boehlen, Fran�oise; Bader, Marlyse; de Moerloose, Philippe // Lupus;2004, Vol. 13 Issue 1, p70
Presents a letter to the editor on antiphospholipid syndrome, a superficial thrombophlebitis of the chest wall associated with anticardiolipin antibodies.
- Tubular aggregates in a patient with primary antiphospholipid syndrome. Spengos, K.; Manta, P.; Sfagos, K.; Vassilopoulos, D. // Lupus;2004, Vol. 13 Issue 7, p555
Presents a letter to the editor regarding primary antiphospholipid syndrome, a thrombophilic state characterized by repeated arterial or venous thrombosis.