Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Bafunno, V"'
Autor:
Bafunno V., Bova M., Loffredo S., Divella C., Petraroli A., Montinaro V., Margaglione M., Triggiani M., LOFFREDO, STEFANIA, MARONE, GIANNI
Publikováno v:
ResearcherID
Summary Hereditary angioedema (HAE) is an autosomal dominant disease due to mutations in the C1 inhibitor gene (C1NH) that affects protein synthesis (HAE type I) or function (HAE type II). In 45 subjects affected by HAE diagnosed through clinical fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec437b080bc68fa0c6095442527ae48
https://doi.org/10.1111/ahg.12052
https://doi.org/10.1111/ahg.12052
Autor:
Bafunno, V.1, Santacroce, R.1, Chetta, M.1, Peyvandi, F.2, Sessa, F.1, Chinni, E.3, Longo, V.1, Margaglione, M.1
Publikováno v:
Haemophilia. Nov2012, Vol. 18 Issue 6, p1003-1007. 5p. 2 Charts.
Autor:
BAFUNNO, V.1 valeria.b@libero.it, SANTACROCE, R.1, CHETTA, M.1, D'ANDREA, G.1, PISANELLI, D.2, SESSA, F.1, TROTTA, T.3, TAGARIELLO, G.4, PEYVANDI, F.5,6, MARGAGLIONE, M.1,2
Publikováno v:
Haemophilia. May2010, Vol. 16 Issue 3, p469-473. 5p. 1 Chart.
Autor:
Cancian, M, Arcoleo, F, Bafunno, V, Barca, Mp, Borrelli, P, Bova, M, Di Rocco PC, Cicardi, M, Cillari, E, De Carolis, C, De Pasquale, T, Del Corso, I, Guarino, Md, Massaro, I, Minale, P, Montinaro, V, Neri, S, Perricone, R, Pucci, S, Quattrocchi, P, Rossi, O, Senter, Riccardo, Triggiani, M, Zanichelli, A, Zanierato, G, Zoli, A.
Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) is a rare disease, with a reported prevalence of about 1 : 50 000. C1-INH-HAE causes disabling symptoms, which may be life-threatening if swelling affects upper airways.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18f437d2842a9cd44b02864bf142621c
http://hdl.handle.net/11386/4675144
http://hdl.handle.net/11386/4675144
Autor:
BAFUNNO, V.1, FAVUZZI, G.2, FIERRO, T.3, CHETTA, M.1, MASTRODICASA, E.4, CHINNI, E.2, GRANDONE, E.2, MARGAGLIONE, M.1, GRESELE, P.3
Publikováno v:
Haemophilia. Mar2012, Vol. 18 Issue 2, pe51-e53. 3p. 1 Diagram, 1 Chart.
Autor:
Bafunno, V., Santacroce, R., Chetta, M., D'Andrea, G., Pisanelli, D., Sessa, F., Trotta, T., Tagariello, G., Peyvandi, F., Margaglione, M.
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(3)
One of the most severe and important complication in the treatment of patients with haemophilia A is the formation of neutralizing antibodies (FVIII inhibitors) that inhibit the clotting activity of substituted FVIII. Both genetic and environmental f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::af607e90fa8f742413689ed10c67a0b9
https://pubmed.ncbi.nlm.nih.gov/20015215
https://pubmed.ncbi.nlm.nih.gov/20015215
New TET2 gene mutations in patients with myeloproliferative neoplasms and splanchnic vein thrombosis
Autor:
COLAIZZO, D., TISCIA, G.L., PISANELLI, D., BAFUNNO, V., AMITRANO, L., GRANDONE, E., GUARDASCIONE, M.A., MARGAGLIONE, M. *
Publikováno v:
In Journal of Thrombosis and Haemostasis May 2010 8(5):1142-1144
Autor:
COLAIZZO, D., TISCIA, G.L., BAFUNNO, V., AMITRANO, L., VERGURA, P., GRANDONE, E., GUARDASCIONE, M.A., MARGAGLIONE, M. *
Publikováno v:
In Journal of Thrombosis and Haemostasis February 2010 8(2):413-416
Publikováno v:
279 (2004): 95–102.
info:cnr-pdr/source/autori:Bafunno V, Giancaspero TA, Brizio C, Bufano D, Passarella S, Boles E, Barile M./titolo:Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export./doi:/rivista:/anno:2004/pagina_da:95/pagina_a:102/intervallo_pagine:95–102/volume:279
info:cnr-pdr/source/autori:Bafunno V, Giancaspero TA, Brizio C, Bufano D, Passarella S, Boles E, Barile M./titolo:Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export./doi:/rivista:/anno:2004/pagina_da:95/pagina_a:102/intervallo_pagine:95–102/volume:279
We have studied the functional steps by which Saccharomyces cerevisiae mitochondria can synthesize FAD from cytosolic riboflavin (Rf). Riboflavin uptake into mitochondria took place via a mechanism that is consistent with the existence of (at least t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::5335083ec761c29cdf278d8b78536275
https://publications.cnr.it/doc/12779
https://publications.cnr.it/doc/12779