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1. Full Text Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age‐matched controls
by Mannucci, Pier Mannuccio and Nobili, Alessandro and Marchesini, Emanuela and Oliovecchio, Emily and Cortesi, Laura and Coppola, Antonio and Santagostino, Elena and Radossi, Paolo and Castaman, Giancarlo and Valdrè, Lelia and Santoro, Cristina and Tagliaferri, Annarita and Ettorre, Cosimo and Zanon, Ezio and Barillari, Giovanni and Cantori, Isabella and Caimi, Teresa Maria and Sottilotta, Gianluca and Peyvandi, Flora and Iorio, Alfonso
Haemophilia, ISSN 1351-8216, 09/2018, Volume 24, Issue 5, pp. 726 - 732
Background In older people, multiple chronic ailments lead to the intake of multiple medications (polypharmacy) that carry a number of negative consequences... 
haemophilia | drug appropriateness | comorbidity | drug interactions | deprescribing | polypharmacy | MORTALITY | DEATH | PEOPLE | HEMATOLOGY | Polypharmacy | Prevalence | Age Factors | Humans | Risk Factors | Female | Male | Hemophilia A - drug therapy | Hemophilia A - pathology | Drugs | Prescribing | Antiviral agents | Comorbidity | Liver | Mortality | Hemophilia | Aged patients | Family medicine | Plants | Comparative analysis | Aging | Liver diseases
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2. Full Text Peripheral circulating cells with paroxysmal nocturnal haemoglobinuria phenotype after a first episode of cerebral sinus vein thrombosis: Results from a multicentre cross-sectional study
by Napolitano, Mariasanta and Santoro, Rita Carlotta and Nicolosi, Daniela and Calafiore, Valeria and Triolo, Anna and Raso, Simona and Parrinello, Laura and Rizzo, Giuseppina and Sottilotta, Gianluca and Siragusa, Sergio and Giuffrida, Gaetano
Thrombosis Research, ISSN 0049-3848, 01/2020, Volume 185, pp. 85 - 87
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3. Full Text Use of catridecacog in a patient with severe factor XIII deficiency undergoing surgery
by Sottilotta, Gianluca and Luise, Francesca and Oriana, Vincenzo and Piromalli, Angela and Santacroce, Rosa and Di Lelio, Alessandra
Hematology Reports, ISSN 2038-8322, 02/2019, Volume 11, Issue 1, pp. 4 - 5
Despite many articles regarding the antihemorrhagic treatment and prophylaxis, there is a lack of experience about how to best conduct major surgical... 
Recombinant FXIII | Surgery | Congenital FXIII deficiency | congenital FXIII deficiency | surgery
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4. Full Text Efficacy of Octocog Alfa (Advate) in a Child with Type 3 von Willebrand Disease and Alloantibodies
by Sottilotta, G and Luise, F and Massara, E and Oriana, V and Piromalli, A and Angela Piromalli and Francesca Luise and Vincenzo Oriana and Gianluca Sottilotta and Elisabetta Massara
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 09/2017, Volume 6, Issue 9, p. 85
Von Willebrand disease (VWD) is the most frequent inherited bleeding disorder and is caused by either a quantitative and/or qualitative defect of the... 
DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | PATIENT | MANAGEMENT | FACTOR VIIA NOVOSEVEN(R) | n/a
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5. Full Text Desensitization and immune tolerance induction in children with severe factor IX deficiency; Inhibitors and adverse reactions to replacement therapy: A case-report and literature review
by Bon, Andrea and Morfini, Massimo and Dini, Alessandro and Mori, Francesca and Barni, Simona and Gianluca, Sottilotta and De Martino, Maurizio and Novembre, Elio
Italian Journal of Pediatrics, ISSN 1720-8424, 2015, Volume 41, Issue 1, p. 12
Hemophilia B is a rare X-linked recessive disorder with plasma factor IX (FIX) deficiency. 1-3% of patients treated with exogenous FIX-containing products... 
Factor IX deficiency | Desensitization | Inhibitor antibodies | Children | Immune tolerance induction | HEMOPHILIA-B PATIENTS | MANAGEMENT | RISK | PEDIATRICS | MECHANISMS | VIII | ANAPHYLAXIS | Factor IX - administration & dosage | Hemophilia B - immunology | Factor IX - immunology | Humans | Immunologic Factors - administration & dosage | Immunologic Factors - immunology | Child, Preschool | Male | Factor IX - adverse effects | Recombinant Proteins - administration & dosage | Hemophilia B - drug therapy | Immune Tolerance - immunology | Immunologic Factors - adverse effects | Desensitization, Immunologic
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6. Full Text Dental Treatment with 30% Trichloroacetic Acid in a Patient with Moderate Hemophilia A
by Delgado, Evelyn Gonzalez and Sottilotta, Gianluca
Open Journal of Blood Diseases, ISSN 2164-3180, 2013, Volume 3, Issue 1, pp. 13 - 14
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7. Full Text Pain assessment and management in haemophilia: A survey among Italian patients and specialist physicians
by Tagliaferri, Annarita and Franchini, Massimo and Rivolta, Gianna F and Farace, Stefania and Quintavalle, Gabriele and Coppola, Antonio and Arbasi, Maria Cristina and Aru, Anna Brigida and Baldacci, Erminia and Bonetti, Elisa and Cantori, Isabella and Cerbone, Anna Maria and Cocco, Antonio and Coluccia, Antonella and Contino, Laura and Cultrera, Dorina and Daniele, Filomena and De Cristofaro, Raimondo and Di Minno, Giovanni and Di Minno, Matteo N.D and Di Perna, Caterina and Ettorre, Cosimo Pietro and Feola, Giulio and Gamba, Gabriella and Giordano, Paola and Giuffrida, Gaetano and Luciani, Matteo and Mancuso, Maria Elisa and Marino, Renato and Molinari, Angelo Claudio and Pasta, Gianluigi and Pedrazzi, Paola and Pizzini, Attilia Maria and Pollio, Berardino and Radossi, Paolo and Raso, Simona and Rodorigo, Giuseppina and Santoro, Rita and Schiavoni, Mario and Schinco, Piercarla and Sottilotta, Gianluca and Speciale, Vincenzo and Todisco, Angelamaria and Turello, Marina and Zanon, Ezio and Ad Hoc Study Grp and ad hoc Study Group and the ad hoc Study Group
Haemophilia, ISSN 1351-8216, 09/2018, Volume 24, Issue 5, pp. 766 - 773
Introduction Persons with haemophilia (PWH) experience recurrent joint bleeding which leads from early synovitis to irreversible joint damage. Pain strongly... 
haemophilia | survey | pain | analgesic | comprehensive care | patient | BLEEDING DISORDERS | ARTHROPATHY | ADULTS | CHILDREN | PROPHYLAXIS | THERAPY | ADOLESCENTS | QUALITY-OF-LIFE | HEMATOLOGY | SEVERITY | Physicians | Humans | Middle Aged | Pain Management - methods | Male | Hemophilia A - pathology | Hemophilia A - complications | Young Adult | Pain Measurement - methods | Adolescent | Adult | Female | Italy | Surveys and Questionnaires | Aged | Child | Chronic Pain - etiology | Surveys | COX-2 inhibitors | Care and treatment | Pain | Fluocinolone acetonide | Opioids | Hemophilia | Chronic pain | Synovitis | Prophylaxis | Inflammation | Management | Patients | Quality of life | Oxygenase | Paracetamol | Children
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8. Full Text Consensus statements on vaccination in patients with haemophilia—Results from the Italian haemophilia and vaccinations (HEVA) project
by Santagostino, Elena and Riva, Agostino and Cesaro, Simone and Esposito, Susanna and Matino, Davide and Mazzucchelli, Renata Ilde and Molinari, Angelo Claudio and Mura, Rosamaria and Notarangelo, Lucia Dora and Tagliaferri, Annarita and Di Minno, Giovanni and Clerici, Mario and Ambaglio, Chiara and Brigida Aru, Anna and Baldacci, Erminia and Barillari, Giovanni and Basso, Maria and Bernasconi, Sayla and Bertamino, Marta and Bertoni, Elisa and Biasoli, Chiara and Federica Biguzzi, Eugenia and Bonetti, Elisa and Borchiellini, Alessandra and Bulgarelli, Simona and Cabibbo, Sergio and Cantori, Isabella and Castaman, Giancarlo and Castiglia, Paolo and Coluccia, Antonella and Coppetelli, Ugo and Coppola, Antonio and Cultrera, Dorina and De Candia, Erica and Delios, Grazia and Di Gennaro, Leonardo and Di Gregorio, Patrizia and Di Minno, Matteo and Dragani, Alfredo and Pietro Ettorre, Cosimo and Franchini, Massimo and Galli, Massimo and Gallo, Giovanni and Giordano, Paola and Giuffrida, Gaetano and Iannaccaro, Piergiorgio and Lassandro, Giuseppe and Lazzareschi, Ilaria and Linari, Silvia and Luciani, Matteo and Macchi, Silvia and Malcangi, Giuseppe and Malizia, Raniero and Marietta, Marco and Marino, Renato and Massoud, Michela and Gabriella Mazzucconi, Maria and Milan, Marta and Morfini, Massimo and Napolitano, Mariasanta and Pasca, Samantha and Pedrazzi, Paola and Peyvandi, Flora A and Piscitelli, Lydia and Pollio, Berardino and Preti, Paola and Quintavalle, Gabriele and Radossi, Paolo and Raso, Simona and Ricca, Irene and Rocino, Angiola and Santoro, Cristina and Carlotta Santoro, Rita and Sarolo, Lucia and Schiavoni, Mario and Schiavulli, Michele and Sciancalepore, Patrizia and Luisa Serino, Maria and Mario Siragusa, Sergio and Sottilotta, Gianluca and Svahn, Johanna and Valdrè, Lelia and Cristina Vedovati, Maria and Zanon, Ezio and HEVA Study Grp and the HEVA Study Group
Haemophilia, ISSN 1351-8216, 07/2019, Volume 25, Issue 4, pp. 656 - 667
Vaccination against communicable diseases is crucial for disease prevention, but this practice poses challenges to healthcare professionals in patients with... 
haemophilia | factor VIII inhibitor | immunization | bleeding disorder | vaccination | BLEEDING DISORDERS | FACTOR-VIII | GUIDELINES | CHILDREN | HEPATITIS-B VACCINATION | INHIBITOR DEVELOPMENT | UPDATE | HEMATOLOGY | VACCINES | Care and treatment | Blood coagulation factor VIII | Communicable diseases | Vaccination | Hemophilia
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9. Full Text Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)
by Collins, Peter and Baudo, Francesco and Knoebl, Paul and Levesque, Herve and Nemes, Laszlo and Pellegrini, Fabio and Marco, Pascual and Tengborn, Lilian and Huth-Kuehne, Angela and Aspoeck, Gerold and Heistinger, Max and Knobl, Paul and Makipernaa, Anne and Ane, Helene and Aouba, A and Bellucci, Sylvia and Beurrier, Philippe and Borg, Jeanne Yvonne and Darnige, Luc and Devignes, Jean and dOiron, Roseline and Gautier, Philippe and Gay, Valerie and Girault, Stephane and Gruel, Yves and Guerin, Viviane and Hezard, Nathalie and Khellaf, Mehdi and Koenig, Martial and Lifermann, Francois and Marlu, Raphael and Ninet, J and Peynet, Jocelyne and Quemeneur, Thomas and Rothschild, Chantal and Schleinitz, Nicolas and Sigaud, Marianne and Trouillier, Sebastien and Voisin, Sophie and Giebl, Aneas and Holstein, Katharina and Huth-Kuhne, Angela and Loreth, Ralph M and Steigerwald, Udo and Tiede, Aneas and Theodossiades, George and Radvanyi, Gaspar and Schlammadinger, Agota and Barillari, Giovanni and Pasca, Samantha and Caimi, T and Contino, L and D'Angelo, Armando and Crippa, Luciano and Fattorini, Annalisa and Di Minno, Giovanni and Cerbone, Anna Maria and Di Minno, Matteo Nicola Dario and D'inca, Marco and Falanga, Anna and Maggioni, Anna and Lerede, Teresa and Franchini, Massimo and Gaidano, Gianluca and De Paoli, Lorenzo and Gamba, Gabriella and Ghirardi, Raffaele and Girotto, Mauro and Tasca, Delios and Grandone, Elvira and Tiscia, Giovanni and Imberti, Davide and Iorio, Alfonso and Landolfi, Raffaele and Di Gennaro, Leonardo and Novarese, Linda and Mariani, Guglielmo and Lapecorella, Mario and Marietta, Marco and Peazzi, Paola and Mazzucconi, Maria Gabriella and Santoro, Cristina and Morfini, Massimo and Linari, Silvia and Moratelli, Stefano and Paolini, Rossella and Piseddu, Gavino and Poggio, Renzo and Pogliani, Enrico and Carpenedo, Monica and Remiddi, Chiara and Santagostino, Elena and Mancuso, Maria Elisa and Santoro, Rita and Papaleo, Giuseppina and Schinco, Piercarla and Borchiellini, Alessana and Valeri, Federica and Scortechini, Anna Rita and Siragusa, Sergio and ...
Blood, ISSN 0006-4971, 07/2012, Volume 120, Issue 1, pp. 47 - 55
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10. Full Text Patient preference for needleless factor VIII reconstitution device: The Italian experience
by Musso, Roberto and Santoro, Rita and Coppola, Antonio and Marcucci, Maura and Sottilotta, Gianluca and Targhetta, Roberto and Zanon, Ezio and Franchini, Massimo
International Journal of General Medicine, ISSN 1178-7074, 2010, Volume 3, pp. 203 - 208
Needlestick injuries, mostly due to unsafe needle devices, are a frequent adverse event among health care workers and patients on chronic treatment, such as... 
Therapy | Kogenate® bayer | Safety | Bio-set | Hemophilia | Patients | Needlestick injuries | hemophilia | Kogenate® Bayer | therapy | safety | Bio-Set
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11. Full Text Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management
by Franchini, Massimo and Castaman, Giancarlo and Coppola, Antonio and Santoro, Cristina and Zanon, Ezio and Di Minno, Giovanni and Morfini, Massimo and Santagostino, Elena and Rocino, Angiola and Abbate, Rosanna and Aru, Anna Brigida and Biasoli, Chiara and Borchiellini, Alessandra and Caimi, Teresa Maria and Cantori, Isabella and Cerbone, Anna Maria and Cesaro, Simone and Ciabatta, Carlo and Coluccia, Antonella and Contino, Laura and Cultrera, Dorina and De Cristofaro, Raimondo and Delios, Grazia and Di Minno, Matteo Nicola Dario and Dragani, Alfredo and Ettorre, Cosimo Pietro and Feola, Giulio and Gamba, Gabriella and Gandini, Giorgio and Giuffrida, Anna Chiara and Giuffrida, Gaetano and Gresele, Paolo and Hassan, Hamisa Jane and Lassandro, Giuseppe and Latella, Caterina and Linari, Silvia and Luciani, Matteo and Mancuso, Maria Elisa and Marchesini, Emanuela and Marino, Renato and Matino, Davide and Mazzucconi, Maria Gabriella and Messina, Maria and Milan, Marta and Molinari, Angelo Claudio and Napolitano, Mariasanta and Notarangelo, Lucia Dora and Peyvandi, Flora and Pollio, Berardino and Radossi, Paolo and Riccardi, Federica and Riva, Silvia and Rivolta, Gianna Franca and Rossetti, Gina and Santoro, Rita Carlotta and Serino, Maria Luisa and Schiavulli, Michele and Schiavoni, Mario and Schinco, Piercarla and Solimeno, Luigi Piero and Sottilotta, Gianluca and Targhetta, Roberto and Tagliaferri, Annarita and Testa, Sophie and Todisco, Angela and Turello, Marina and Valdrè, Lelia and AICE Working Grp and AICE Working Group
Blood Transfusion, ISSN 1723-2007, 07/2015, Volume 13, Issue 3, pp. 498 - 513
SYSTEMIC-LUPUS-ERYTHEMATOSUS | SINGLE-CENTER EXPERIENCE | IMMUNOSUPPRESSIVE THERAPY | FACTOR-VIII INHIBITORS | HEMOPHILIA REGISTRY EACH2 | FACTOR-X DEFICIENCY | FACTOR-IX | PORCINE FACTOR-VIII | INTERNATIONAL REGISTRY | HEMATOLOGY | VON-WILLEBRAND-SYNDROME | Autoantibodies - blood | Humans | Female | Male | Hemophilia A - diagnosis | Hemophilia A - therapy | Hemophilia A - blood | Blood Coagulation Factor Inhibitors - blood | Recommendation
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12. Full Text Recombinant Activated Factor VII Combined with Desmopressin in Preventing Bleeding from Dental Extraction in a Patient with Glanzmann’s Thrombasthenia
by Lombardo, Vincenzo Trapani and Sottilotta, Gianluca
Clinical and Applied Thrombosis/Hemostasis, ISSN 1076-0296, 01/2006, Volume 12, Issue 1, pp. 115 - 116
The case of a 41-year-old woman with Glanzmann’s thrombasthenia who underwent double dental extraction is presented. In the past, treatments with desmopressin... 
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13. Full Text Hyperhomocysteinemia and C677T MTHFR Genotype in Patients With Retinal Vein Thrombosis
by Sottilotta, Gianluca and Siboni, Simona Maria and Latella, Caterina and Oriana, Vincenzo and Romeo, Ermelinda and Santoro, Rita and Consonni, Dario and Trapani Lombardo, Vincenzo
Clinical and Applied Thrombosis/Hemostasis, ISSN 1076-0296, 10/2010, Volume 16, Issue 5, pp. 549 - 553
Introduction: Elevated homocysteine (Hcy) is associated with the risk of deep vein thrombosis, pulmonary embolism, ischemic heart disease, and stroke. Several... 
Thrombophilia | Gene polymorphisms | Venous thromboembolism | thrombophilia | POPULATION | RISK-FACTOR | venous thromboembolism | MUTATION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | PLASMA HOMOCYSTEINE | gene polymorphisms | VASCULAR-DISEASE | OCCLUSION | Genetic Predisposition to Disease | Hyperhomocysteinemia - blood | Humans | Middle Aged | Risk Factors | Genotype | Male | Retinal Vein Occlusion - blood | Retinal Vein Occlusion - genetics | Case-Control Studies | Polymorphism, Genetic | Young Adult | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Aged, 80 and over | Adult | Female | Hyperhomocysteinemia - genetics | Aged | Retrospective Studies | Cohort Studies
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14. Full Text High Incidence of Factor V Leiden and Prothrombin G20210A in Healthy Southern Italians
by Sottilotta, Gianluca and Mammì, Corrado and Furlò, Giuseppe and Oriana, Vincenzo and Latella, Caterina and Trapani Lombardo, Vincenzo
Clinical and Applied Thrombosis/Hemostasis, ISSN 1076-0296, 06/2009, Volume 15, Issue 3, pp. 356 - 359
Factor V Leiden (FVL) and G20210 prothrombin (FII G20210A) mutations are risk factors for thromboembolism. In Europe, FVL is more prevalent in the north (7%)... 
Thrombophilia | Factor V Leiden | Prothrombin G20210 | thrombophilia | factor V Leiden | POPULATION | ORIGIN | VENOUS THROMBOEMBOLISM | GENE | prothrombin G20210 | PERIPHERAL VASCULAR DISEASE | PREVALENCE | MUTATIONS | 3-UNTRANSLATED REGION | HEMATOLOGY | European Continental Ancestry Group - genetics | Gene Frequency | Humans | Male | Reference Values | Polymorphism, Genetic | Homozygote | Adult | Female | Heterozygote | Italy | Prothrombin - genetics | Factor V - genetics
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15. Full Text Patient preference for needleless factor VIII reconstitution device: The Italian experience
by Musso, Roberto and Santoro, Rita and Coppola, Antonio and Marcucci, Maura and Sottilotta, Gianluca and Targhetta, Roberto and Zanon, Ezio and Franchini, Massimo
American Journal of Clinical Hypnosis, ISSN 0002-9157, 04/2011, Volume 53, Issue 4, pp. 203 - 208
Therapy | Kogenate® bayer | Bio-set | Hemophilia | Safety
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16. Full Text Congenital hypodysfibrinogenemia and abruptio placentae in a woman with history of cerebral thrombosis
by Santoro, Rita and Iannaccaro, Piergiorgio and sottilotta, Gianluca
Acta Obstetricia et Gynecologica Scandinavica, ISSN 0001-6349, 2007, Volume 86, Issue 2, pp. 247 - 248
Pregnancy | Thrombophilia | Hypodysfibrinogenemia | Hemorrhage | Abruptio placentae | thrombophilia | DYSFIBRINOGENEMIA | hypodysfibrinogenemia | FETAL LOSS | pregnancy | AFIBRINOGENEMIA | abruptio placentae | hemorrhage | OBSTETRICS & GYNECOLOGY | Abruptio Placentae | Humans | Stillbirth | Anticoagulants - therapeutic use | Heparin - therapeutic use | Enoxaparin - therapeutic use | Warfarin - therapeutic use | Puerperal Disorders - drug therapy | Puerperal Disorders - etiology | Intracranial Thrombosis - etiology | Fibrinogens, Abnormal - adverse effects | Adult | Female | Intracranial Thrombosis - drug therapy
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17. Full Text The prothrombin time/international normalized ratio (PT/INR) Line: derivation of local INR with commercial thromboplastins and coagulometers - two independent studies
by Poller, L and Ibrahim, S and Keown, M and Pattison, A and Jespersen, J and Marun, S and Muntean, W and Aspoeck, Gerold and Gallus, Alex S and Bailleul, E and Wijns, William and Michel, T and Jochmans, Kristin and Chatelain, B and Marcelis, Carlo L. M and Nijs de, A.S and Johnston, M and Kynde, K and Syrjala, M and Savolainen, E.-R and Ivaska, K and Rajamaki, A and Vanharanta, R and Juhan, I and Aillaud, M.-F and Guillin, M.-C and Huisse, M.-G and Sie, P and Lecompte, T and Schmitt, Y and Harenberg, J and Plesch, W and Aronis, S and Theodossiades, George and Tsoukanas, B and Markala, D and Ditsa, M and Cahill, M and Madden, M and White, B and Nolan, B.T and Fitzgerald, H and McCarthy, D and Collins, B and Rooney, S and Naparstek, E and Palareti, G and Marongiu, F and Erba, N and Testa, Sophie and Mariani, G and Poti, R and Mannucci, P. M and Tripodi, A and Bader, R and Pengo, Vittorio and Gresele, Paolo and D'inca, Marco and Ageno, W and Tosetto, Alberto and Hensgens, H. E. S. J and Idema, R. N and Oosterhout, D. H and Mulder, A. B and Hamulyak, K and van der Dussen, H and Musial, J and Gago, T and Palmeiro, A and Campos, Manuel and Marques-Dias, D. A and Monteiro, A. Cunha and Cunha, M. Angela and de Gaia, W. N and Peternel, P and Stegnar, M and Fontcuberta, J and Borrell, M and Reverter, J. C and Santasusana, P. Domenech and Lopez-Fernandez, M. Fernanda and Castro-Montero, José Luis and Ribera Casado, C and Vicente, Vicente and Edlund, B and Egberg, N and Laemmle, B and Alberio, L and de Moerloose, P and Reber, G and Machin, S. J and Mackie, I and Lawrie, A and Luckit, J and Shanks, D and Dolan, G and Flaherty, T and Ludlam, C. A and Walker, I. D and Lawson, D. E and ... and European Action Anticoagulation and European Action On Anticoagulation
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 01/2011, Volume 9, Issue 1, pp. 140 - 148
Background: The WHO scheme for prothrombin time (PT) standardization has been limited in application, because of its difficulties in implementation,... 
INR correction | prothrombin time | coagulometers | ECAA plasmas | thromboplastins | INR Line | PT/INR Line | Coagulometers | Prothrombin time | Thromboplastins | MULTICENTER | PLASMA CALIBRANTS | FIELD | ENHANCED STANDARDIZATION | INTERNATIONAL SENSITIVITY INDEX | QUALITY ASSESSMENT | PERIPHERAL VASCULAR DISEASE | TIME MONITORS | HEMATOLOGY | ISI | Prothrombin Time - standards | Predictive Value of Tests | Rabbits | Reproducibility of Results | World Health Organization | Humans | Automation, Laboratory - standards | Linear Models | Thromboplastin - analysis | Calibration | International Normalized Ratio - standards | Reference Standards | Animals | Analysis of Variance | Cattle | Blood Coagulation | Observer Variation | Medical examination | Chemical tests and reagents | Prothrombin | Thrombin | Anticoagulants (Medicine) | Universities and colleges | Blood
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18. Iliac giant pseudotumour in a haemophiliac patient
by Rita Santoro and Piergiorgio Iannaccaro and Gianluca Sottilotta and Pier Paolo Arcuri
British Journal of Haematology, ISSN 0007-1048, 07/2004, Volume 126, Issue 2, p. 163
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19. Full Text Iliac giant pseudotumour in a haemophiliac patient
by Santoro, Rita and Iannaccaro, Piergiorgio and Sottilotta, Gianluca and Arcuri, Pier Paolo
British Journal of Haematology, ISSN 0007-1048, 07/2004, Volume 126, Issue 2, pp. 163 - 163
HIV Infections - diagnostic imaging | Psoas Muscles - pathology | Hemophilia A - diagnostic imaging | Humans | Hematoma - diagnostic imaging | Hematoma - diagnosis | Hematoma - etiology | Male | Tomography, X-Ray Computed | Psoas Muscles - diagnostic imaging | Hemophilia A - pathology | Hemophilia A - complications | Muscular Diseases - etiology | Muscular Diseases - diagnosis | Magnetic Resonance Imaging | Ilium - diagnostic imaging | HIV Infections - pathology | HIV Infections - complications | Ilium - pathology | Adult | Hepatitis C - complications | Hepatitis C - diagnostic imaging | Hepatitis C - pathology | Muscular Diseases - diagnostic imaging
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20. Full Text Recombinant activated factor VII combined with desmopressin in preventing bleeding from dental extraction in a patient with Glanzmann's thrombasthenia
by Lombardo, Vincenzo Trapani and Sottilotta, Gianluca
Clinical and Applied Thrombosis/Hemostasis, ISSN 1076-0296, 01/2006, Volume 12, Issue 1, pp. 115 - 116
The case of a 41-year-old woman with Glanzmann's thrombasthenia who underwent double dental extraction is presented. In the past, treatments with desmopressin... 
Glanzmann's thrombasthenia | Dental extraction | Recombinant activated factor VII | dental extraction | DDAVP | DISORDERS | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | recombinant activated factor VII | Recombinant Proteins - therapeutic use | Blood Loss, Surgical - prevention & control | Tooth Extraction - methods | Factor VII - therapeutic use | Humans | Adult | Female | Thrombasthenia - complications | Drug Therapy, Combination | Deamino Arginine Vasopressin - therapeutic use | Factor VIIa
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