Zobrazeno 1 - 10
of 29
pro vyhledávání: '"F Marafioti"'
Autor:
M. Cirillo, A. Prigiobbo, Mario Barra, Antonio Cassinese, R. Vaglio, Roberto Russo, F Marafioti
Publikováno v:
Superconductor Science and Technology. 17:S427-S431
In this paper the performances of superconducting devices based on fractal layout are discussed. Depending on their shape, fractals are characterized by self-similarity and/or space-filling properties. The former allows the design of superconducting
Autor:
Gina Rossetti, P Gottardi, N Ceschini, F Marafioti, C Mazzon, Paola Boccagni, M Antolini, M Rubertelli, G Gosetti
Publikováno v:
The International Journal of Artificial Organs. 16:139-142
New systems for collection of platelet concentrate (PC) and platelet poor plasma (PPP) are presently available. The aim of our work was to test the possibility of preparing PC routinely from normal plasma donors in a minimum amount of time and, at th
Autor:
M, Rubertelli, F, Marafioti, C, Mazzon, G, Rossetti, G, Gosetti, P, Gottardi, M, Antolini, N, Ceschini, P, Boccagni
Publikováno v:
The International journal of artificial organs. 16
New systems for collection of platelet concentrate (PC) and platelet poor plasma (PPP) are presently available. The aim of our work was to test the possibility of preparing PC routinely from normal plasma donors in a minimum amount of time and, at th
Publikováno v:
Acta Haematologica. 72:73-82
A family with a new congenital abnormality of antithrombin III (AT III) is presented. 5 members, all females, were affected. The proposita has had several thrombotic manifestations. The other patients
Publikováno v:
Acta haematologica. 75(1)
Heterozygous plasminogen deficiency was found in 2 patients (mother and daughter). The mother, aged 55 years, was symptomatic while the daughter, aged 10 years, was asymptomatic so far. The thrombotic tendency presented by the proposita (mother) was
Publikováno v:
Haematologia. 20(3)
In this study we present a new case of Factor XIII deficiency. The proposita, a 34 year old woman, showed a deficiency of both subunit a and subunit b, and a moderate bleeding tendency. Because of the concomitant decrease of subunits a and b the prop
In a family with a known antithrombin III abnormality (AT III Trento) an associated von Willebrand defect (Type I) was found. The two defects seem to segregate independently. In fact four types of individuals were present, namely: subjects with isola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1dadd87edacb80739f731593b3b398e
http://hdl.handle.net/11577/2489915
http://hdl.handle.net/11577/2489915
Publikováno v:
Rivista italiana di ginecologia.
Publikováno v:
Archivio di ostetricia e ginecologia. 87(3-4)