Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Emanuele Allemand"'
Autor:
P. Bigolin, Fabrizio Fabris, Fabio De Stefano, Alois Saller, Emanuele Allemand, Giuseppe Realdi
Publikováno v:
Aging Clinical and Experimental Research. 24:97-103
Tako-tsubo cardiomyopathy (idiopathic or transient left ventricular apical ballooning syndrome [ABS]) is a reversible condition frequently precipitated by a stressful trigger that clinically mimics an acute ST-elevation myocardial infarction. Charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9aa56fb408375c1159cebbe6b200965
https://doi.org/10.1007/bf03325357
https://doi.org/10.1007/bf03325357
Publikováno v:
European Journal of Haematology. 86:135-139
FVII Padua is a Type 2 defect owing to an Arg304Gln substitution in exon 8. The defect was originally discovered in an isolated valley in northeastern Italy. Subsequently, it was described in several other countries of the Mediterranean basin and Mid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bfb6a5c8b335cdbddc42f23f2732424
https://doi.org/10.1111/j.1600-0609.2010.01544.x
https://doi.org/10.1111/j.1600-0609.2010.01544.x
Publikováno v:
Haemophilia. 16:182-185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32622425f6ac08181f215ee399926a6b
https://doi.org/10.1111/j.1365-2516.2009.02091.x
https://doi.org/10.1111/j.1365-2516.2009.02091.x
Autor:
Silvia Vettore, Fabrizio Fabris, Emanuele Allemand, Maria Luigia Randi, Mario Plebani, Raffaella Scandellari
Publikováno v:
Blood Coagulation & Fibrinolysis. 20:108-113
The aims of this study were to assess the prevalence of Helicobacter pylori infection in chronic idiopathic thrombocytopenic purpura adult patients and investigate the platelet response after eradication. To minimize the confounding effect of concomi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18ea254775097e6b4d84f36ad76fa6b5
https://doi.org/10.1097/mbc.0b013e32832315d8
https://doi.org/10.1097/mbc.0b013e32832315d8
Publikováno v:
Haemophilia. 15:825-827
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b7430b22e51f8f4ed0c622125f02b7f
https://doi.org/10.1111/j.1365-2516.2008.01959.x
https://doi.org/10.1111/j.1365-2516.2008.01959.x
Autor:
Fabiana Tezza, Martina Treleani, Fabrizio Vianello, Fabrizio Fabris, Michela Galdarossa, Pamela Scarparo, Emanuele Allemand
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 23(4)
Administrative databases can be a reliable source for estimating the epidemiology of blood disorders. No data are available estimating the epidemiology of thrombocytopenia from administrative data in Italian institutions. We analyzed the administrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b666a0cdd670a497474cb7d1013518fe
https://pubmed.ncbi.nlm.nih.gov/22343688
https://pubmed.ncbi.nlm.nih.gov/22343688
Autor:
Irene Bertozzi, Maria Luigia Randi, Giulia Berti de Marinis, Emanuele Allemand, Fabrizio Fabris, Agostino Naso, Fabiana Tezza
Publikováno v:
Internal and emergency medicine. 7(5)
Dr. Berti de Marinis, Dr. Allemand: In November 2009, a 40-year-old man was urgently hospitalized after orthostatic syncope secondary to severe hypotension. Three days before admission, he had experienced profuse sweating and contracted diuresis afte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77e32a47e3825e492e7651a442461d2
https://pubmed.ncbi.nlm.nih.gov/21948352
https://pubmed.ncbi.nlm.nih.gov/21948352
Autor:
Antonio Girolami, Bruno Girolami, Anna Maria Lombardi, Emanuele Allemand, Raffaella Scandellari
Publikováno v:
Hematology (Amsterdam, Netherlands). 14(3)
The Gla-domain of factor X (FX) is a 39 residue peptide, part of the light chain, and is characterized by the presence of 11 gamma-carboxylglutaminic acid residues interspersed among other no-Gla residues. At least 15 cases of FX deficiency have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fedf6e6827108a8bcba8b6558133e69f
https://pubmed.ncbi.nlm.nih.gov/19490765
https://pubmed.ncbi.nlm.nih.gov/19490765
Publikováno v:
American journal of hematology. 83(8)
Congenital Factor X deficiency is commonly classified as type I, in which there is a concomitant decrease of activity and antigen (CRM negative), and in type II, in which activity is low but antigen is normal or near normal (CRM positive). During the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dae5253a98df776f1ae9ab0ffded152d
https://pubmed.ncbi.nlm.nih.gov/18785643
https://pubmed.ncbi.nlm.nih.gov/18785643
Publikováno v:
Acta haematologica. 117(1)
Factor VII deficiency is the least rare among uncommon congenital coagulation disorders. The majority of cases are isolated deficiencies. In some cases, FVII deficiency has been found to be associated with the deficiency in another coagulation factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ad8a10a8408d60ba786fcb4eae28c0
https://pubmed.ncbi.nlm.nih.gov/17095860
https://pubmed.ncbi.nlm.nih.gov/17095860