Zobrazeno 1 - 10
of 346
pro vyhledávání: '"M, Margaglione"'
Publikováno v:
Value in Health. 22:S851
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c31ada1b1a88a6c81de6993d3a17ff
https://doi.org/10.1016/j.jval.2019.09.2386
https://doi.org/10.1016/j.jval.2019.09.2386
Autor:
E, Grandone, D, Colaizzo, G, Tiscia, P, Vergura, F, Cappucci, L, Greco, M, Margaglione, P, Martinelli, G M, Maruotti
Summary. Background: Although an association between thrombophilias and adverse pregnancy outcome has been shown, the influence of the most common inherited thrombophilias and the somatic mutation JAK2 V617F in determining an adverse outcome is quest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::537d36b5d0f3759748159134e2ddfa1f
http://hdl.handle.net/11588/378493
http://hdl.handle.net/11588/378493
Autor:
D. DELUCIA, V. DELGIUDICE, M. LAURETANO, G. MAISTO, R. MAROTTA, M. MARGAGLIONE, E. GRANDONE, M. L. PAPA, LEPORE, Maria Antonietta
Bechet's disease may be considered an immune-mediated vasculitis involving vessels of all size. We would like to suggest that Bechet's disease should be considered as a prethrombotic state. Howerer, we feel that the hypercoagulable/prethrombotic stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::d3fda91cfe6cb630e2c672b85adcca60
http://hdl.handle.net/11591/183820
http://hdl.handle.net/11591/183820
Autor:
D. DELUCIA, V. DELGIUDICE, M. QUARANTIELLO, M. LAURETANO, G. MAISTO, R. MAROTTA, M. MARGAGLIONE, E. GRANDONE, M. L. PAPA, LEPORE, Maria Antonietta
In the cases presented herein, the TIA episode occurred in the setting of a long history of migraine. Our findings suggest that in a sample of Southern Italy population, aPL are independently associated with the risk for TIA episode.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::e832daa6ea17384462548b3e2c5ec3fa
http://hdl.handle.net/11591/166170
http://hdl.handle.net/11591/166170
Autor:
M, Tomaiuolo, G, Favuzzi, F, Cappucci, D, Pisanelli, G L, Tiscia, P, Musto, F A, Scaraggi, R I, Cincione, M, Margaglione, E, Grandone
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(5)
Factor XI (FXI) deficiency is a rare bleeding disorder, resulting in a wide range of bleeding manifestations, from asymptomatic bleeding to injury-related bleeding. To identify mutations in FXI-deficient patients and to establish a possible relations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0757f0e19b5e68ebb758bb015f854565
https://pubmed.ncbi.nlm.nih.gov/20491955
https://pubmed.ncbi.nlm.nih.gov/20491955
Publikováno v:
Clinical and laboratory haematology. 24(1)
Myeloproliferative disorders are the main cause of Budd-Chiari syndrome in western countries. Inherited or acquired thrombophilic factors have also been implicated. A novel mutation of the prothrombin gene (G--A20210) has only been described in a few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::663c10a0e0ba20887039bb52adf7e1c2
https://pubmed.ncbi.nlm.nih.gov/11843901
https://pubmed.ncbi.nlm.nih.gov/11843901
Autor:
S, De Cosmo, M, Margaglione, V, Tassi, M, Garrubba, S, Thomas, C, Olivetti, G P, Piras, R, Trevisan, M, Vedovato, P, Cavallo Perin, S, Bacci, D, Colaizzo, C, Cisternino, L, Zucaro, G, Di Minno, V, Trischitta, G C, Viberti
Genetic factors are involved in the development of diabetic nephropathy in Type 1 diabetes. We have examined the association of four candidate genes, angiotensin converting enzyme (ACE): insertion/deletion (I/D) polymorphism, plasminogen activator in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ab47b3e6e9affa83bce18000af3e0995
http://hdl.handle.net/11588/477236
http://hdl.handle.net/11588/477236
Autor:
E, Grandone, M, Margaglione, D, Colaizzo, G, Cappucci, D, Paladini, P, Martinelli, S, Montanaro, G, Pavone, G, Di Minno
Publikováno v:
Thrombosis and haemostasis. 77(6)
We performed a case-controlled study to investigate whether the FV Leiden mutation and the CT677 polymorphism of the 5, 10 methylene tetrahydrofolate reductase (MTHFR) are associated with the occurrence of preeclampsia in 96 otherwise healthy preecla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d1ef8ba159cb6aff40f1e8b79378e20
https://pubmed.ncbi.nlm.nih.gov/9241730
https://pubmed.ncbi.nlm.nih.gov/9241730
Autor:
Norman K. Hollenberg, Steven W. Graves, Robert B. McCall, William T. Jackson, Jerome H. Fleisch, M. Margaglione, E. Grandone, F. P. Mancini, G. Di Minno, N. Seiler, A. Hardy, J. P. Moulinoux, James Claghorn, Michael D. Lesem, Eric J. Lien, Arima Das, Linda L. Lien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91e28ed26266d1d0de42de29a07955ca
https://doi.org/10.1007/978-3-0348-8996-4
https://doi.org/10.1007/978-3-0348-8996-4