VETTORE, SILVIA

VETTORE, SILVIA  

Dipartimento di Medicina - DIMED  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
MOLECULAR AND CELLULAR DIVERSITY OF HEART CONDUCTION SYSTEM MYOCYTES 1994 GORZA, LUISAVETTORE, SILVIA + TRENDS IN CARDIOVASCULAR MEDICINE - -
Cardiac myocytes differ in mRNA composition for sarcoplasmic reticulum Ca2+ channels and Ca2+ pumps. 1995 GORZA, LUISAVETTORE, SILVIAVOLPE, POMPEO + ANNALS OF THE NEW YORK ACADEMY OF SCIENCES - -
Intracellular Ca2+ -release channel mRNA composition of the developing, adult and senescent rat heart 1996 GORZA, LUISAVETTORE, SILVIA + - - -
Neurofilament M mRNA is expressed in conduction system myocytes of the developing and adult rabbit heart 1996 VETTORE, SILVIAGORZA, LUISA + JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY - -
Regional and age-related differences in mRNA composition of intracellular Ca2+-release channels of rat cardiac myocytes. 1997 GORZA, LUISAVETTORE, SILVIA + JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY - -
Impairment of fibrinolytic potential in long-term steroid treatment after heart transplantation. 1997 CASONATO, SANDRAVETTORE, SILVIAGIROLAMI, ANTONIO + TRANSPLANTATION - -
Selection of both normal and bleeding patients is indicated before desmopressin administration 2005 GIROLAMI, ANTONIOVETTORE, SILVIAFABRIS, FABRIZIO THROMBOSIS AND HAEMOSTASIS - -
Helicobater pylori infection and clinical response to eradication therapy in patients with immune thrombocytopenic purpura (ITP) 2005 FABRIS, FABRIZIOVETTORE, SILVIARANDI, MARIA LUIGIA + BLOOD - -
Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature. 2006 GIROLAMI, ANTONIOVETTORE, SILVIACASONATO, SANDRA + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Novel point mutation in a leucine-rich repeat of the GP1balfa chain of the platelet von Willebrand factor receptor, GP1b/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant 2008 VETTORE, SILVIAMORO, STEFANORANDI, MARIA LUIGIAFABRIS, FABRIZIO + HAEMATOLOGICA - -
Heparin induced-thrombocytopenia in patients with myeloproliferative disorders 2008 RANDI, MARIA LUIGIADUNER, ELENAVETTORE, SILVIAFABRIS, FABRIZIO + HEMATOLOGY JOURNAL - -
Caratterizzazione Molecolare delle Macrotrombocitopenie Ereditarie a Trasmissione Autosomica Dominante 2008 Vettore, Silvia - - -
Platelet response to Helicobacter pylori eradication therapy in adult chronic idiopathic thrombocytopenic purpura seems to be related to the presence of anticytotoxin-associated gene A antibodies. 2009 SCANDELLARI, RAFFAELLAALLEMAND, EMANUELEVETTORE, SILVIAPLEBANI, MARIORANDI, MARIA LUIGIAFABRIS, FABRIZIO BLOOD COAGULATION & FIBRINOLYSIS - -
Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia 2010 FABRIS, FABRIZIOVETTORE, SILVIARANDI, MARIA LUIGIA + THROMBOSIS AND HAEMOSTASIS - -
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect. 2010 VETTORE, SILVIAFABRIS, FABRIZIO + EUROPEAN JOURNAL OF MEDICAL GENETICS - -
Identification of patients with thrombocytopenia in padua university and city hospital through the administrative database 2010 VETTORE, SILVIAFABRIS, FABRIZIO + HEMATOLOGY JOURNAL - -
Bernard Boulier syndrome in a patients affected by klinefelter disease: novel a386g homosygous mutation of gpib alpha gene with anomalous behaviour 2010 VETTORE, SILVIAMORO, STEFANOFABRIS, FABRIZIO + THE HEMATOLOGY JOURNAL - -
Clinical biological remission induced by rituximab in acute refractory chronic relapsing TTP. 2010 VETTORE, SILVIAGIROLAMI, ANTONIOFABRIS, FABRIZIO + THROMBOSIS RESEARCH - -
Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes). 2011 GIROLAMI, ANTONIOVETTORE, SILVIABONAMIGO, EMANUELAFABRIS, FABRIZIO JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard-Soulier syndrome. 2012 Girolami AVettore SVIANELLO, FABRIZIOBerti de Marinis GFABRIS, FABRIZIO JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -