Zobrazeno 1 - 10
of 54
pro vyhledávání: '"J. A. Winkelstein"'
Publikováno v:
Veterinary Pathology. 31:201-206
Genetically determined deficiencies of the early components of the classical complement pathway (Cl, C4, C2) or of the third component of complement (C3) in both human beings and experimental animals are known to be associated with renal disease, inc
Autor:
Peter Q. Eichacker, W. D. Hoffman, L. C. Cork, Charles Natanson, Zenaide M.N. Quezado, C A Koev, Ronald J. Elin, I. Yatsiv, J. A. Winkelstein
Publikováno v:
The Journal of Experimental Medicine
We investigated whether the third component of complement (C3) is involved in the pathophysiology of endotoxic shock, and if it is involved, whether it plays a protective role or whether it mediates shock and multiple organ failure. In a prospective,
Publikováno v:
Infection. 32(6)
We describe a 54-year-old man with X-linked agammaglobulinemia (XLA) and Helicobacter cinaedi bacteremia, who presented with tender, hyper-pigmented skin macules without increased local warmth or fever. We propose that this presentation may be a char
Autor:
K L, O'Brien, A J, Swift, J A, Winkelstein, M, Santosham, B, Stover, R, Luddy, J E, Gootenberg, J T, Nold, A, Eskenazi, S J, Snader, H M, Lederman
Publikováno v:
Pediatrics. 106(5)
To determine the immunogenicity and safety of heptavalent pneumococcal polysaccharide vaccine (serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) conjugated to CRM(197) (7-valent conjugate pneumococcal vaccine [7VPnC]) among infants with sickle cell disease
Autor:
H, Ozsahin, F X, Arredondo-Vega, I, Santisteban, H, Fuhrer, P, Tuchschmid, W, Jochum, A, Aguzzi, H M, Lederman, A, Fleischman, J A, Winkelstein, R A, Seger, M S, Hershfield
Publikováno v:
Blood. 89(8)
Adenosine deaminase (ADA) deficiency typically causes severe combined immunodeficiency (SCID) in infants. We report metabolic, immunologic, and genetic findings in two ADA-deficient adults with distinct phenotypes. Patient no. 1 (39 years of age) had
Autor:
K E, Sullivan, J J, Wisnieski, J A, Winkelstein, J, Louie, E, Sachs, R, Choi, E, Veksler, D, Goldman, M, Petri
Publikováno v:
The Journal of rheumatology. 23(12)
To determine whether complement component analyses during a period of inactive disease can define clinically important subgroups and predict morbidity in patients with systemic lupus erythematosus (SLE).We identified 277 patients with SLE whose disea
Autor:
M B, Fasano, K E, Sullivan, S B, Sarpong, R A, Wood, S M, Jones, C J, Johns, H M, Lederman, M J, Bykowsky, J M, Greene, J A, Winkelstein
Publikováno v:
Medicine. 75(5)
The true incidence of sarcoidosis in common variable immunodeficiency (CVID) is unknown. We report here 8 cases of sarcoidosis among 80 patients with CVID followed in our clinics, along with 22 well-documented cases reported in the literature. Sarcoi
Publikováno v:
Transplantation. 61(8)
This study focuses upon two discrete components of posttransplant hepatic reticuloendothelial system (RES) function-phagocytosis and killing of bacteria-under various conditions of ischemic preservation. We had previously reported that, following int
Publikováno v:
The Journal of rheumatology. 21(6)
In an effort to establish whether a 28 base pair (bp) deletion in the gene for the 2nd component of complement (C2) constitutes a significant genetic risk factor for systemic lupus erythematosus (SLE), we determined the frequency of this mutation in
Publikováno v:
Chest. 101(4)
A 19-year-old woman with a childhood history of cavitating left upper lobe pneumonia presented with persistent weight loss, fever, cough and roentgenographic evidence of right upper lobe pneumonia resistant to antibiotic therapy. An open lung biopsy