Search Results - "MERLINI, G"
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Consensus guidelines for the conduct and reporting of clinical trials in systemic light-chain amyloidosis
Published in Leukemia (01-11-2012)“…This manuscript summarizes the recommendations that emerged from the first Roundtable on Clinical Research in Immunoglobulin Light-chain Amyloidosis (AL), a…”
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Light chain amyloidosis: the heart of the problem
Published in Haematologica (Roma) (01-10-2013)Get full text
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AL Amyloidosis
Published in Clinical lymphoma, myeloma and leukemia (01-09-2015)Get full text
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AA amyloidosis: basic knowledge, unmet needs and future treatments
Published in Swiss medical weekly (31-05-2012)“…Systemic AA amyloidosis is a long-term complication of several chronic inflammatory disorders, including rheumatoid arthritis, ankylosing spondylitis,…”
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The systemic amyloidoses: clearer understanding of the molecular mechanisms offers hope for more effective therapies
Published in Journal of internal medicine (01-02-2004)“… Knowledge about the systemic amyloidoses has increased considerably during the last few years. This group of diseases is characterized by great biochemical…”
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Melphalan and dexamethasone with or without bortezomib in newly diagnosed AL amyloidosis: a matched case–control study on 174 patients
Published in Leukemia (01-12-2014)“…Oral melphalan and dexamethasone (MDex) is a standard treatment for patients with AL amyloidosis who are not eligible for stem cell transplantation at many…”
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Rationale, application and clinical qualification for NT-proBNP as a surrogate end point in pivotal clinical trials in patients with AL amyloidosis
Published in Leukemia (01-10-2016)“…Amyloid light-chain (LC) amyloidosis (AL amyloidosis) is a rare and fatal disease for which there are no approved therapies. In patients with AL amyloidosis,…”
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Amyloidosis: is a cure possible?
Published in Annals of oncology (01-06-2008)Get full text
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Early data on long‐term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2‐year update from the open‐label extension of the NEURO‐TTR trial
Published in European journal of neurology (01-08-2020)“…Background and purpose Hereditary transthyretin (hATTR) amyloidosis causes progressive polyneuropathy resulting from transthyretin (TTR) amyloid deposition…”
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International uniform response criteria for multiple myeloma
Published in Leukemia (01-09-2006)“…New uniform response criteria are required to adequately assess clinical outcomes in myeloma. The European Group for Blood and Bone Marrow…”
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Management of treatment-emergent peripheral neuropathy in multiple myeloma
Published in Leukemia (01-04-2012)“…Peripheral neuropathy (PN) is one of the most important complications of multiple myeloma (MM) treatment. PN can be caused by MM itself, either by the effects…”
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Diagnosis, treatment, and response assessment in solitary plasmacytoma: updated recommendations from a European Expert Panel
Published in Journal of hematology and oncology (16-01-2018)“…Solitary plasmacytoma is an infrequent form of plasma cell dyscrasia that presents as a single mass of monoclonal plasma cells, located either extramedullary…”
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Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma
Published in Leukemia (01-08-2017)“…Immunoglobulin light chain (AL) amyloidosis is characterized by tissue deposition of amyloid fibers derived from immunoglobulin light chain. AL amyloidosis and…”
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Bortezomib in the treatment of AL amyloidosis: targeted therapy?
Published in Haematologica (Roma) (01-10-2007)Get full text
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The combination of thalidomide and intermediate-dose dexamethasone is an effective but toxic treatment for patients with primary amyloidosis (AL)
Published in Blood (01-04-2005)“…Based on the efficacy of thalidomide in multiple myeloma and on its synergy with dexamethasone on myeloma plasma cells, we evaluated the combination of…”
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A revised international prognostic score system for Waldenström’s macroglobulinemia
Published in Annals of oncology (01-10-2018)Get full text
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P56 SURVIVAL BENEFIT OF BIRTAMIMAB IN MAYO STAGE IV AL AMYLOIDOSIS IN THE PHASE 3 VITAL STUDY WAS CONSISTENT ACROSS ALL KEY BASELINE VARIABLES
Published in HemaSphere (09-05-2023)Get full text
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P1714: HEALTHCARE RESOURCE UTILIZATION IN PATIENTS WITH LIGHT CHAIN AMYLOIDOSIS IN EUROPE
Published in HemaSphere (23-06-2022)Get full text
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Bortezomib in a phase 1 trial for patients with relapsed AL amyloidosis: cardiac responses and overall effects
Published in QJM : An International Journal of Medicine (01-11-2011)“…Background: Bortezomib is approved for the treatment of multiple myeloma and a role has been suggested in the treatment of systemic AL amyloidosis (AL)…”
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