Zobrazeno 1 - 10
of 23
pro vyhledávání: '"J Palermos"'
Publikováno v:
Calcified Tissue International. 68:285-290
Bisphosphonates are potent inhibitors of osteoclastic activity and reduce the disease-related skeletal complications when they are used in combination with chemotherapy in patients with multiple myeloma (MM). Pamidronate also inhibits apoptosis of pr
Autor:
A. N. Maniatis, J. Palermos, Maria Kantzanou, N. A. Maniatis, C. Christodoulou, Nicholas J. Legakis
Publikováno v:
Journal of Medical Microbiology. 44:199-202
The significance of Streptococcus agalactiae as an aetiological agent in vaginitis was evaluated. A total of 6226 samples from women who presented with vaginal symptoms was examined. The presence of >10 leucocytes/high-power field (h.p.f.) was taken
Autor:
E, Terpos, J, Palermos, K, Tsionos, K, Anargyrou, N, Viniou, P, Papassavas, J, Meletis, X, Yataganas
Publikováno v:
European journal of haematology. 65(5)
Bisphosphonates are potent inhibitors of osteoclastic activity and are used in the treatment of multiple myeloma (MM) in combination with chemotherapy. The effect of pamidronate on markers of bone resorption [cross-linked N-telopeptides of type I col
Autor:
A. N. Maniatis, N. A. Maniatis, J. Palermos, Nicholas J. Legakis, G. Katsanis, Ioannis P. Trougakos
Publikováno v:
Chemotherapy. 43(1)
Surveillance data on 12,944 bacterial isolates derived from nosocomial infections, reported to the Department of Microbiology and Infectious Diseases of the Hellenic Air Force and VA General Hospital over a 9-year period (1986-1994), were analyzed by
Autor:
B O Barger, Harry W. Schroeder, John E. Volanakis, F M Schaffer, Rodney C.P. Go, Z B Zhu, K J Macon, R. D. Campbell, J Palermos, Max D. Cooper
We have proposed that significant subsets of individuals with IgA deficiency (IgA-D) and common variable immunodeficiency (CVID) may represent polar ends of a clinical spectrum reflecting a single underlying genetic defect. This proposal was supporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35856edad8439dd91b48d5e904e724e3
https://europepmc.org/articles/PMC295891/
https://europepmc.org/articles/PMC295891/
Publikováno v:
Progress in Immunology ISBN: 9783642837579
IgA deficiency (IgA-D) and common variable immunodeficiency (CVID) are heritable disorders both of which feature an arrest in B cell differentiation. IgA-D is characterized by a normal number of immature IgA-bearing B cells which fail to undergo diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d88fe0043d836c7b9b42bb7336f0d07
https://doi.org/10.1007/978-3-642-83755-5_72
https://doi.org/10.1007/978-3-642-83755-5_72
IgA deficiency and common variable immunodeficiency are heritable disorders that can occur within the same family. Both immunodeficiencies are characterized by arrests in B-cell differentiation that vary in the extent of the immunoglobulin isotypes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb0950dcd11f4b9991317b9398110ea
https://europepmc.org/articles/PMC298204/
https://europepmc.org/articles/PMC298204/
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