Zobrazeno 1 - 7
of 7
pro vyhledávání: '"S A, Vogelgesang"'
Autor:
S. A. Vogelgesang, Sandra S. Richter, A. J. Chavez, Amy M. Grooters, Michael G. Rinaldi, M. A. Pfaller, Aaron D. Bossler, G.S. de Hoog, Deanna A. Sutton
Publikováno v:
Journal of Clinical Microbiology. 41:4779-4782
A 62-year-old male with a history of Wegener's granulomatosis and immunosuppressive therapy presented with chronic olecranon bursitis. A black velvety mould with brown septate hyphae and tapered annellides was isolated from a left elbow bursa aspirat
Autor:
B, Kovacs, T, Szentendrei, J M, Bednarek, M C, Pierson, J D, Mountz, S A, Vogelgesang, G C, Tsokos
Publikováno v:
Clinical and experimental rheumatology. 15(1)
To report a patient with SLE whose T cells expressed disproportionally increased amounts of an alternatively spliced form of Fas/APO1 transcript and secreted a soluble form of Fas.We established continuously activated, short-term T cell lines from 16
Autor:
S A, Vogelgesang, M P, Heyes, S G, West, A M, Salazar, P P, Sfikakis, R N, Lipnick, G L, Klipple, G C, Tsokos
Publikováno v:
The Journal of rheumatology. 23(5)
To evaluate the relationship between quinolinic acid, a neuroactive metabolite of L-tryptophan, and neuropsychiatric manifestations of systemic lupus erythematosus (SLE).Forty specimens of cerebrospinal fluid (CSF) were obtained from 39 patients with
Publikováno v:
The Journal of rheumatology. 22(7)
We describe 2 patients in whom juvenile dermatomyositis (DM) was associated with well defined clinical polyneuropathies, and review the clinical and serological data. Light and electron microscopy were used to study muscle and nerve tissues from one
Publikováno v:
The Journal of rheumatology. 22(4)
We describe a patient with rheumatoid arthritis who developed bacteremia from Listeria monocytogenes after treatment with low dose oral pulse methotrexate. We discuss possible immunologic mechanisms for susceptibility to Listeria infections. As the e
Autor:
S A, Vogelgesang, G L, Klipple
Publikováno v:
Postgraduate medicine. 96(5)
Amyloidosis occurs in association with many diseases and can also be idiopathic. It is usually a systemic disease with variable presentations. The diagnosis should be suspected in patients with unexplained proteinuria, cardiomyopathy, congestive hear
Publikováno v:
South Dakota journal of medicine. 39(6)