Zobrazeno 1 - 10
of 53
pro vyhledávání: '"D. Belvini"'
Akademický článek
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Autor:
Paolo Radossi, Patrizia Pontisso, M. Gerotto, R. Salviato, G. Tagariello, D. Belvini, Alfredo Alberti
Publikováno v:
Haemophilia. 10:81-86
Summary. Patients with haemophilia show high prevalence of hepatitis C infection but low rate of progressive liver disease when they are not co-infected with HIV. The balance between host immune system and hepatitis C virus (HCV) variability seems to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61b41521d8c14aeb4b524d102e55f6bf
https://doi.org/10.1046/j.1365-2516.2003.00846.x
https://doi.org/10.1046/j.1365-2516.2003.00846.x
Publikováno v:
Haemophilia. 8:17-21
Haemophilia A displays a broad heterogeneity of genetic defects and of clinical severity. Inhibitor development is the main complication of replacement therapy in severe cases and most patients with inhibitors have gross gene rearrangement or point m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75973f42b1e4544679db3a8d3055ca29
https://doi.org/10.1046/j.1365-2516.2002.00578.x
https://doi.org/10.1046/j.1365-2516.2002.00578.x
Autor:
Antonio Girolami, Fabrizio Vianello, F. Dal Bello, Ezio Zanon, Giuseppe Tagariello, P. Zerbinati, D. Belvini, Anna M. Lombardi
Publikováno v:
Haemophilia. 7:511-514
Haemophilia B patients with factor IX (FIX) activity < 1% are usually characterized by severe bleeding episodes early in life. We report a case of sporadic severe haemophilia B, clinically characterized by mild bleeding diathesis. The presence of ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::becd74fc11a0f65541a23dea186781c2
https://doi.org/10.1046/j.1365-2516.2001.00551.x
https://doi.org/10.1046/j.1365-2516.2001.00551.x
Publikováno v:
Haemophilia. 10:194-196
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404a520cfadee72a7efe41a3b613c72c
https://doi.org/10.1111/j.1365-2516.2003.00855.x
https://doi.org/10.1111/j.1365-2516.2003.00855.x
Autor:
Ezio Zanon, Giancarlo Castaman, F. Pierobon, Giorgio Gandini, Paolo Radossi, Roberto Sartori, D. Zanotto, D. Belvini, R. Salviato, G. Tagariello
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 13(4)
Summary. Anti factor VIII (FVIII) antibodies represent the main complication of replacement therapy in severe cases of haemophilia and most patients with inhibitor have gross gene rearrangements or point mutations that hamper the production of normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8f2516187f99c4e56e49fbe2d71af22
https://pubmed.ncbi.nlm.nih.gov/17610549
https://pubmed.ncbi.nlm.nih.gov/17610549
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 8(1)
Haemophilia A displays a broad heterogeneity of genetic defects and of clinical severity. Inhibitor development is the main complication of replacement therapy in severe cases and most patients with inhibitors have gross gene rearrangement or point m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b13c3b80a59dea6f1dd09cbc095e7a3
https://pubmed.ncbi.nlm.nih.gov/11886460
https://pubmed.ncbi.nlm.nih.gov/11886460
Autor:
F, Vianello, D, Belvini, F, Dal Bello, G, Tagariello, E, Zanon, A M, Lombardi, P, Zerbinati, A, Girolami
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 7(5)
Haemophilia B patients with factor IX (FIX) activity1% are usually characterized by severe bleeding episodes early in life. We report a case of sporadic severe haemophilia B, clinically characterized by mild bleeding diathesis. The presence of anamne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95a1aa393f9aaa130eeb087dfd59e392
https://pubmed.ncbi.nlm.nih.gov/11952854
https://pubmed.ncbi.nlm.nih.gov/11952854
Publikováno v:
Haemophilia. 7:603-604
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f31bf561436c5495348b8ac144e6b4fa
https://doi.org/10.1046/j.1365-2516.2001.00572.x
https://doi.org/10.1046/j.1365-2516.2001.00572.x