Search Results - "Colella, Marina P"

Key endothelial cell angiogenic mechanisms are stimulated by the circulating milieu in sickle cell disease and attenuated by hydroxyurea by Lopes, Flavia C M, Traina, Fabiola, Almeida, Camila B, Leonardo, Flavia C, Franco-Penteado, Carla F, Garrido, Vanessa T, Colella, Marina P, Soares, Raquel, Olalla-Saad, Sara T, Costa, Fernando F, Conran, Nicola

“…As hypoxia-induced inflammatory angiogenesis may contribute to the manifestations of sickle cell disease, we compared the angiogenic molecular profiles of…”
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Elevated hypercoagulability markers in hemoglobin SC disease by Colella, Marina P, de Paula, Erich V, Machado-Neto, João A, Conran, Nicola, Annichino-Bizzacchi, Joyce M, Costa, Fernando F, Olalla Saad, Sara T, Traina, Fabiola

“…Hemoglobin SC disease is a very prevalent hemoglobinopathy; however, very little is known about this condition specifically. There appears to be an increased…”
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Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease by Ataga, Kenneth I, Kutlar, Abdullah, Kanter, Julie, Liles, Darla, Cancado, Rodolfo, Friedrisch, João, Guthrie, Troy H, Knight-Madden, Jennifer, Alvarez, Ofelia A, Gordeuk, Victor R, Gualandro, Sandra, Colella, Marina P, Smith, Wally R, Rollins, Scott A, Stocker, Jonathan W, Rother, Russell P

“…In this yearlong trial involving patients with sickle cell disease, crizanlizumab, an antibody to P-selectin, was associated with a 45% lower rate of pain…”
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Chronic pain in patients with hemophilia: Influence of kinesiophobia and catastrophizing thoughts by Feldberg, Glenda, Ricciardi, Janaína B.S., Zorzi, Alessandro R., Colella, Marina P., Yamaguti‐Hayakawa, Gabriela G., Ozelo, Margareth C.

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A retrospective analysis of 122 immune thrombocytopenia patients treated with dapsone: Efficacy, safety and factors associated with treatment response by Colella, Marina P., Orsi, Fernanda A., Alves, Elizio C. F., Delmoro, Gabriela de F., Yamaguti‐Hayakawa, Gabriela G., Paula, Erich V., Annichino‐Bizzacchi, Joyce M.

“…Background The optimum second‐line treatment or best sequence of treatments for immune thrombocytopenia (ITP) are yet to be determined. Our institution has…”
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Aquatic exercise in patients with haemophilia: Electromyographic and functional results from a prospective cohort study by Feldberg, Glenda, Ricciardi, Janaína B. S., Zorzi, Alessandro R., Colella, Marina P., Ozelo, Margareth C.

“…Introduction Recurrent joint bleeds in haemophilia patients often cause musculoskeletal changes leading to functional capacity impairment. Aim In this study,…”
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Residual Vein Thrombosis Echogenicity Is Associated to the Risk of DVT Recurrence: A Cohort Study by Mazetto, Bruna M., Orsi, Fernanda L. A., Silveira, Sandra A. F., Bittar, Luis F., Flores-Nascimento, Mariane M. C., Zapponi, Kiara C. S., Colella, Marina P., de Paula, Erich V., Annichino-Bizzacchi, Joyce M.

“…Although deep vein thrombosis (DVT) recurrence is a common late complication of the disease, there are few predictive markers to risk-stratify patients…”
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Elevated plasma levels and platelet-associated expression of the pro-thrombotic and pro-inflammatory protein, TNFSF14 (LIGHT), in sickle cell disease by Garrido, Vanessa T., Proença-Ferreira, Renata, Dominical, Venina M., Traina, Fabiola, Bezerra, Marcos A. C., de Mello, Mariana R. B., Colella, Marina P., Araújo, Aderson S., Saad, Sara T. O., Costa, Fernando F., Conran, Nicola

“…Summary Chronic vascular inflammation and endothelial activation may initiate vaso‐occlusion in sickle cell disease (SCD). TNFSF14 (CD258; LIGHT), a…”
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Severe postthrombotic syndrome is associated with characteristic sonographic pattern of the residual thrombosis by Mazetto, Bruna M, Orsi, Fernanda L.A, Silveira, Sandra A.F, Bittar, Luis Fernando, Flores-Nascimento, Mariane C, Zapponi, Kiara C.S, Colella, Marina P, de Paula, Erich V, Annichino-Bizzacchi, Joyce M

“…Postthrombotic syndrome (PTS) may affect 50% of patients with deep venous thrombosis, 5–10% of them may present severe manifestations. The causes for PTS…”
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Performance of a point-of-care device in determining prothrombin time in an anticoagulation clinic by Colella, Marina P, Fiusa, Maiara M.L, Orsi, Fernanda L.A, de Paula, Erich V, Annichino-Bizzacchi, Joyce M

“…New portable devices for the measurement of the prothrombin time and the international normalized ratio (INR) from capillary blood samples have demonstrated to…”
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Acquired Hemophilia a Relapse Is Related to Th2 Response, and Increased Expression of B-Cell Activating Factor (BAFF) by Frade-Guanaes, Jessica O, Racanelli, Ana P, Siqueira, Lucia H, Costa-Lima, Carolina, Medina, Samuel S, Foschi, Nivia M, Colella, Marina P, Montalvão, Silmara A L, Yamaguti-Hayakawa, Gabriela G, Ozelo, Margareth C

“…Acquired hemophilia A (AHA) is a rare autoimmune disorder caused by the development of autoantibodies against the factor (F)VIII of coagulation with higher…”
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Impact of Two Immobilized GPIbα Assays in the Diagnosis of Von Willebrand Disease by Montalvão, Silmara Lima, Soares, Sandra Martins Silva, Colella, Marina P, Annichino-Bizzacchi, Joyce M, Medina, Samuel de Souza, Ozelo, Margareth C

“…The diagnosis of von Willebrand Disease (VWD) remains a challenge of daily hematology practice. Ristocetin cofactor activity (VWF:RCo) is an important…”
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Lower Echogenicity of the Residual Venous Thrombosis at Ultrasound Examination Is Associated to Recurrent Thrombosis Events by Mazetto, Bruna M, Orsi, Fernanda Loureiro de Andrade, Silveira, Sandra A.F, Zapponi, Kiara Cristina Senger, Colella, Marina P, de Paula, Erich Vinicius, Annichino-Bizzachi, Joyce

“…Introduction: After the first thrombotic event, up to 30% of deep venous thrombosis (DVT) cases may recur within 10 years. Unprovoked first DVT episode, male…”
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Six Novel Mutations Identified in the Glycoproteins Ib Alpha, Ib Beta and IX Genes Among Twenty-Two Unrelated Patients with Bernard-Soulier Syndrome in Brazil by de Siqueira, Lucia Helena, Beltrame, Miriam P, Cunha, Fernanda P G, Colella, Marina P, Annichino-Bizzacchi, Joyce M, de Paula, Erich V, Ozelo, Margareth C.

“…Abstract 1156▪▪This icon denotes a clinically relevant abstract Bernard-Soulier syndrome (BSS) is a rare hereditary bleeding disorder, caused by mutations…”
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Comparative Evaluation of Five Different Assays for Ristocetin Cofactor Activity Determination by Montalvao, Silmara Aparecida Lima, Faioto, Vanessa Boury, Colella, Marina P, Machado, Tania de Fatima Gomes Siegl, Annichino-Bizzacchi, Joyce M, De Paula, Erich V, Ozelo, Margareth C.

“…Abstract 3317 Despite significant advances in the comprehension of the molecular pathogenesis of Von Willebrand Disease (VWD), the diagnosis of this condition…”
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Hydroxyurea Reduces the Hypercoagulable State In Sickle Cell Anemia by Colella, Marina P, Machado-Neto, Joao, Quaino, Susan K.P., Conran, Nicola, Annichino-Bizzacchi, Joyce M, Costa, Fernando Ferreira, Saad, Sara Olalla, de Paula, Erich V, Traina, Fabiola

“…Abstract 1068 Sickle cell anemia (SCA) is associated with a hypercoagulable state, through mechanisms not yet clearly defined. SCA patients present an elevated…”
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Elevation of Hypercoagulability Markers in Hemoglobin SC Disease by Colella, Marina P, De Paula, Erich V, Conran, Nicola, Machado-Neto, João, Quaino, Susan K.P., Annichino-Bizzacchi, Joyce M, Costa, Fernando Ferreira, Saad, Sara T Olalla, Traina, Fabiola

“…Abstract 3227 Sickle cell anemia (SCA) patients present an elevated rate of thrombotic complications and increased biological markers of hemostatic activation…”
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Elevated plasma levels and platelet‐associated expression of the pro‐thrombotic and pro‐inflammatory protein, T NFSF14 (LIGHT), in sickle cell disease by Garrido, Vanessa T., Proença‐Ferreira, Renata, Dominical, Venina M., Traina, Fabiola, Bezerra, Marcos A. C., de Mello, Mariana R. B., Colella, Marina P., Araújo, Aderson S., Saad, Sara T. O., Costa, Fernando F., Conran, Nicola

“…Summary Chronic vascular inflammation and endothelial activation may initiate vaso‐occlusion in sickle cell disease ( SCD ). TNFSF 14 ( CD 258; LIGHT ), a…”
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