Zobrazeno 1 - 10
of 29
pro vyhledávání: '"P J Späth"'
Publikováno v:
Revista de la Facultad de Medicina Veterinaria y de Zootecnia, Vol 68, Iss 3, Pp 189-199 (2021)
El objetivo de este trabajo fue evaluar in vitro la eficacia del extracto de quebracho (Schinopsis spp.), rico en taninos condensados, en el control de H. contortus de ovinos, ya que existen evidencias de que estos taninos pueden reducir la excreció
Externí odkaz:
https://doaj.org/article/fffe80a4b7e343f781dca73ad49e98be
Autor:
Makoto Sudo, Yoshiki Yamaguchi, Peter J Späth, Kana Matsumoto-Morita, Benjamin K Ong, Nortina Shahrizaila, Nobuhiro Yuki
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e107772 (2014)
Intravenous immunoglobulin (IVIG) is the first line treatment for Guillain-Barré syndrome and multifocal motor neuropathy, which are caused by anti-ganglioside antibody-mediated complement-dependent cytotoxicity. IVIG has many potential mechanisms o
Externí odkaz:
https://doaj.org/article/8acd0e57836d44f987d0de17f76ac6b2
Publikováno v:
Allergy. 56:349-358
A 54-YEAR-OLD woman was referred to the allergy unit of the department of dermatology at University Hospital Zurich for a diagnostic work-up after she had emergency treatment for an episode of angioedema of the tongue and throat. Angioedematous sympt
Autor:
H.-J. Späth
Publikováno v:
Eiszeitalter und Gegenwart, Vol 23-24, Pp 130-140 (1973)
Zwischen Melvich und Cape Wrath an der Nordküste Sutherlands wurden solche morphologischen Phänomene erfaßt und ausgewertet, die auf postglaziale Meeresstände zurückzuführen sind. Die vertikale Verteilung dieser Formen konzentriert sich auf vie
Externí odkaz:
https://doaj.org/article/80de25f3d75a49ba9125aed7d7278f06
Publikováno v:
The Journal of Immunology. 158:5043-5049
The ninth component of human complement (C9) is the last of the terminal complement components creating the membrane attack complex. C9 is a single-chain serum protein that is encoded by a gene located on chromosome 5p. Deficiency of terminal complem
Publikováno v:
Vox Sanguinis. 59:51-58
The complement system, as the effector mechanism of the antigen-antibody reaction, and the levels of circulating immune complexes in a 1-year, double-blind, randomized, placebo-controlled study served as laboratory parameters to assess the effect of
Publikováno v:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 49(2)
A multicentre, retrospective study of hereditary deficiency of C1-esterase inhibitor (C1-INH) function, a deficiency which clinically manifests as hereditary angioedema (HAE), was performed in six centres in Germany, Austria and Switzerland. 242 indi
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 86(9)
Seventy-seven children with bacterial meningitis were screened for complement deficiency. Both the classical and the alternate pathways were normal in 75 patients. Transiently reduced total haemolytic activity of the classical pathway was documented
Publikováno v:
Blood. 88(1)
Intravenously applied human IgG has beneficial effects in treating inflammatory diseases, presumably because it has a complement attenuating role. This role of IgG was studied in vitro by following C3 activation and inactivation in sera that were sup
Autor:
D, Agardi, M, Pigg, A G, Sjöholm, L, Truedsson, P J, Späth, E J, Kuijper, C C, Tijssen, L, Tranebjaerg, K H, Gustavson, P J, Ulfendahl
Publikováno v:
Experimental and clinical immunogenetics. 12(2)
Microsatellite polymorphisms are widely used to map the genes responsible for inherited disorders. The most commonly used detection is based on radioactive labelling and autoradiography. We now present the successful detection of fluorescence-labelle