Search Results - "Brodsky, Andres"
-
1
Genetic Variants in C5 and Poor Response to Eculizumab
Published in The New England journal of medicine (13-02-2014)“…Patients with paroxysmal nocturnal hemoglobinuria who had a poor response to eculizumab therapy were found to have a genetic polymorphism in C5 that prevents…”
Get full text
Journal Article -
2
-
3
Apoptotic synergism between STI571 and the farnesyl transferase inhibitor SCH66336 on an imatinib-sensitive cell line
Published in Blood (01-03-2003)Get full text
Journal Article -
4
Sudden sensorineural hearing loss as a manifestation of primary antiphospholipid syndrome
Published in Joint, bone, spine : revue du rhumatisme (01-07-2007)Get full text
Journal Article -
5
DELAYED ERYTHROID AND PLATELET RESPONSE TO ECULIZUMAB IN PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA – A CASE REPORT AND LITERATURE REVIEW
Published in European medical journal. Hematology (01-08-2013)“…Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired clonal disorder of haemopoiesis characterised by haemolytic anaemia, thrombophilia and variable…”
Get full text
Journal Article -
6
Long‐term safety and efficacy of ravulizumab in patients with paroxysmal nocturnal hemoglobinuria: 2‐year results from two pivotal phase 3 studies
Published in European journal of haematology (01-09-2022)“…Objectives The complement component 5 (C5) inhibitor ravulizumab demonstrated non‐inferiority to eculizumab following 26 weeks of treatment in complement…”
Get full text
Journal Article -
7
Phase 3 randomized COMMODORE 2 trial: Crovalimab versus eculizumab in patients with paroxysmal nocturnal hemoglobinuria naive to complement inhibition
Published in American journal of hematology (01-09-2024)“…Crovalimab is a novel C5 complement inhibitor that enables rapid and sustained C5 inhibition with subcutaneous, low‐volume self‐administration every 4 weeks…”
Get full text
Journal Article -
8
Eculizumab in paroxysmal nocturnal hemoglobinuria with Budd-Chiari syndrome progressing despite anticoagulation
Published in Experimental hematology & oncology (06-09-2012)“…Paroxysmal nocturnal hemoglobinuria (PNH) is a progressive, life-threatening disorder characterized by chronic intravascular hemolysis caused by uncontrolled…”
Get full text
Journal Article -
9
Eculizumab Treatment of Paroxysmal Nocturnal Hemoglobinuria Relapsing After Bone Marrow Transplant and Subsequent Clonal: Case Report
Published in Blood (18-11-2011)“…Abstract 5274 Paroxysmal nocturnal hemoglobinuria (PNH) is a chronic and life-threatening hematopoietic stem cell disorder characterized by deficiency of the…”
Get full text
Journal Article -
10
Ham Test For Therapeutic Monitoring Of Eculizumab In Paroxysmal Nocturnal Hemoglobinuria
Published in Blood (15-11-2013)“…Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired clonal disease, caused by an inactivating mutation in the PIG-A gene in a hematopoietic stem cell…”
Get full text
Journal Article -
11
"M3-M6" Molecular Response Evolution As Early Predictor of Outcome Considering Generic Vs Branded TKIs for Chronic Myeloid Leukemia (CML): An Argentine Multicentric Study
Published in Blood (02-12-2016)“…Introduction: Early reduction of BCR-ABL transcript level has been associated with improved outcomes in CML treatment. Inability to achieve early molecular…”
Get full text
Journal Article -
12
Eculizumab Treatment of Paroxysmal Nocturnal Hemoglobinuria (PNH). the Argentinian Experience
Published in Blood (03-12-2015)“…paroxysmal nocturnal hemoglobinuria (PNH) is a clonal, non malignant disease of hematopoiesis characterized by intravascular hemolysis, a variable depth of…”
Get full text
Journal Article -
13
Rapid desensitization and slow recovery of the cyclic AMP response mediated by histamine H2 receptors in the U937 cell line
Published in Biochemical pharmacology (15-07-2000)Get full text
Journal Article -
14
Coversin is effective in the treatment of PNH with resistance to eculizumab due to complement C5 polymorphism
Published in Immunobiology (1979) (01-10-2016)Get full text
Journal Article -
15
Rapid desensitization and slow recovery of the cyclic AMP response mediated by histamine H 2 receptors in the U937 cell line
Published in Biochemical pharmacology (15-07-2000)“…The present study focused on the desensitization process of the H 2 receptor in U937 cells and the recovery of the cyclic AMP (cAMP) response. Treatment of…”
Get full text
Journal Article -
16
Histamine modulates the expression of c-fos through cyclic AMP production via the H2 receptor in the human promonocytic cell line U937
Published in Molecular pharmacology (01-06-1997)“…We examined the effects of histamine and its agonists on the expression of the c-fos and c-myc proto-oncogenes at the transcriptional and translational levels…”
Get more information
Journal Article -
17
Feno-genotipificación de trombocitopenias hereditarias: nuestra experiencia en 50 familias
Published in Hematología (En línea) (2020)“…Diagnosis of inherited thrombocytopenias represents a true challenge owing to heterogeneity of these disorders and the absence of distinctive features in…”
Get full text
Journal Article -
18
Sudden sensorineural hearing loss as a manifestation of primary antiphospholipid syndrome
Published in Joint bone spine (01-07-2007)Get full text
Report -
19
MANAGEMENT RECOMMENDATIONS FOR DIRECT ORAL ANTICOAGULANTS (DOACs) ANTI Xa AND ANTI IIa
Published in Medicina (01-03-2022)“…Direct oral anticoagulants have emerged as the drugs that have changed the management of the antithrombotic treatment in the last 15 years. Their advantages,…”
Get more information
Journal Article -
20
Forskolin induces U937 cell line differentiation as a result of a sustained cAMP elevation
Published in European journal of pharmacology (29-05-1998)“…The present study examines the effects of forskolin on U937 cell differentiation. We recently reported that dibutyryl cAMP (dbcAMP), but not cAMP-elevating…”
Get full text
Journal Article