Sfoglia per Autore
Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis
2010 C. Vener, C. Novembrino, F. Bamonti, N.S. Fracchiolla, U. Gianelli, F. Savi, F. Radaelli, E. Fermo, A. Cortelezzi, S. Lonati, M. Menegatti, G. Lambertenghi Deliliers
Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis
2010 I. Martinelli, P. Bucciarelli, V. De Stefano, S.M. Passamonti, M. Menegatti, D. Tormene, A. Tosetto, P.M. Mannucci
Patients Informative Booklet on the Establishment of a European Network of Rare Bleeding Disorders (EN-RBD) project funded by EC (downloadable at www.rbdd.eu)
2011 F. Peyvandi, R. Palla, M. Menegatti, S. Malosio
Registri nazionali ed internazionali sulle malattie rare della coagulazione
2011 F. Peyvandi, A. Cairo, R. Palla, M. Menegatti
Post-partum haemorrhage in women with rare bleeding disorders
2011 F. Peyvandi, M. Menegatti, S.M. Siboni
Gynecological and obstetrical manifestations of inherited bleeding disorders in women
2011 F. Peyvandi, I. M. Garagiola, M. Menegatti
Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran
2012 P. Eshghi, N. Cohan, M. Lak, M. Naderi, F. Peyvandi, M. Menegatti, M. Karimi
Inherited bleeding disorders in pregnancy: rare coagulation factor defects
2012 F. Peyvandi, M. Menegatti, S. Siboni
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes
2012 L.A. LOTTA, M. WANG, J. YU, I. MARTINELLI, F. YU, S.M. PASSAMONTI, D. CONSONNI, E. PAPPALARDO, M. MENEGATTI, S.E. SCHERER, L.L. LEWIS, H. AKBAR, Y. WU, M.N. BAINBRIDGE, D.M. MUZNY, P.M. MANNUCCI, R.A. GIBBS, F. PEYVANDI
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran
2012 M. Karimi, A. Vafafar, S. Haghpanah, M. Payandeh, P. Eshghi, H. Hoofar, A. Afrasiabi, J. Gerdabi, R. Ardeshiri, M. Menegatti, F. Peyvandi
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders : results from the European Network of Rare Bleeding Disorders
2012 F. Peyvandi, R. Palla, M. Menegatti, S.M. Siboni, S. Halimeh, B. Faeser, H. Pergantou, H. Platokouki, P. Giangrande, K. Peerlinck, T. Celkan, N. Ozdemir, C. Bidlingmaier, J. Ingerslev, M. Giansily-Blaizot, J.F. Skeved, R. Gilmore, A. Gadisseur, M. Benedik-Dolnicar, L. Kitanovsky, D. Mikovic, K.M. Musallam, F.R. Rosendaal
Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disorders
2012 M. Van Geffen, M. Menegatti, A. Loof, P. Lap, M. Karimi, B.A. Laros-van Gorkom, P. Brons, W.L. Van Heerde
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene
2013 M. Menegatti, D. Balestra, B. Fabrizzi, R. Asselta, M. Pinotti, F. Peyvandi
A recurrent Gly43Asp substitution of coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking
2013 M. Menegatti, R. De Cristofaro, A. Vangone, R. Palla, G. Milano, L. Cavallo, R. Oliva, F. Peyvandi
Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management
2013 F. Peyvandi, M. Menegatti, R. Palla
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene
2013 M. Menegatti, D. Balestra, B. Fabrizzi, R. Asselta, M. Pinotti, F. Peyvandi
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency
2013 L.A. Lotta, S.M. Siboni, L. Lemma, M. Clerici, M. Menegatti, F. Peyvandi
Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran
2014 M. Karimi, A. Cairo, M. Safarpour, S. Haghpanah, M. Ekramzadeh, A. Afrasiabi, M. Shahriari, M. Menegatti
Thrombin Generation in Patients with Idiopathic Sudden Sensorineural Hearing Loss
2014 A. Tripodi, P. Capaccio, L. Pignataro, V. Chantarangkul, M. Menegatti, F. Bamonti, M. Clerici, R. De Giuseppe, F. Peyvandi
Combined Factor V and Factor VIII Deficiency in Rare Coagulation Disorders
2014 F. Peyvandi, R. Palla, M. Menegatti
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