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Proteomics in molecular diagnosis: typing of amyloidosisAmyloid diseases of the heart: current and future therapiesDifferences in immunoglobulin light chain species found in urinary exosomes in light chain amyloidosis (Al)Amyloidosis and POEMS syndrome.Increased serum free light chains precede the presentation of immunoglobulin light chain amyloidosis.Macroglossia due to Systemic Amyloidosis: Is There a Role for Radiotherapy?The amyloidoses: clinical features, diagnosis and treatment.Senile cardiac amyloidosis: an underappreciated cause of heart failure.A detailed evaluation of the current renal response criteria in AL amyloidosis: is it time for a revision?Light-chain amyloidosis: SCT, novel agents and beyond.New insights and modern treatment of AL amyloidosis.Immunoglobulin light chain amyloidosis.Future directions in the clinical management of amyloid light-chain amyloidosis.Pre-transplantation novel agent induction predicts progression-free survival for patients with immunoglobulin light-chain amyloidosis undergoing high-dose melphalan and autologous stem cell transplantation.The impact of dialysis on the survival of patients with immunoglobulin light chain (AL) amyloidosis undergoing autologous stem cell transplantation.Predictors of inferior clinical outcome in patients with standard-risk multiple myeloma.Increasing the accuracy of proteomic typing by decellularisation of amyloid tissue biopsies.Long-term outcomes of primary systemic light chain (AL) amyloidosis in patients treated upfront with bortezomib or lenalidomide and the importance of risk adapted strategies.A Very Rare Presentation of Multiple Myeloma: Unilateral Raccoon Eye.The prognostic value of diagnosing concurrent multiple myeloma in immunoglobulin light chain amyloidosis.Bortezomib and dexamethasone consolidation following risk-adapted melphalan and stem cell transplantation for patients with newly diagnosed light-chain amyloidosis.Pulmonary masses in a patient with dyspnea: Apply Occam's razor or Hickam's dictum?Clinical characteristics and long-term outcome of patients with POEMS syndrome in China.Trend toward improved day 100 and two-year survival following stem cell transplantation for AL: a comparison before and after 2006.AbstractsMacroglossia – not always AL amyloidosis
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 17 July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
How I treat amyloidosis.
@en
How I treat amyloidosis.
@nl
type
label
How I treat amyloidosis.
@en
How I treat amyloidosis.
@nl
prefLabel
How I treat amyloidosis.
@en
How I treat amyloidosis.
@nl
P1433
P1476
How I treat amyloidosis.
@en
P2093
Raymond L Comenzo
P304
P356
10.1182/BLOOD-2009-04-202879
P407
P577
2009-07-17T00:00:00Z