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P50 | author | Morie A Gertz | Q57052163 |
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International Myeloma Working Group guidelines for serum-free light chain analysis in multiple myeloma and related disorders | Q34884527 | ||
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Transplantation for amyloidosis | Q36726168 | ||
Revised prognostic staging system for light chain amyloidosis incorporating cardiac biomarkers and serum free light chain measurements | Q36910372 | ||
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Amyloidosis: 2008 BMT Tandem Meetings (February 13-17, San Diego). | Q37045900 | ||
Changes in serum-free light chain rather than intact monoclonal immunoglobulin levels predicts outcome following therapy in primary amyloidosis | Q37172003 | ||
Laryngeal amyloidosis causing hoarseness and airway obstruction | Q37359127 | ||
Cardiac amyloidosis in a patient with multiple myeloma: a case report and review of literature. | Q37379828 | ||
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Cardiac amyloidosis: approaches to diagnosis and management | Q37654514 | ||
Echocardiographic evaluation of cardiac amyloid | Q37738051 | ||
Treatment of immunoglobulin light chain amyloidosis | Q37738576 | ||
Pitfalls in the diagnosis of primary amyloidosis | Q37761568 | ||
Systemic amyloidosis: a challenge for the rheumatologist | Q37763504 | ||
Renal outcome and monoclonal immunoglobulin deposition disease in 289 old patients with blood cell dyscrasias: a single center experience | Q37767014 | ||
Asymptomatic immunoglobulin light chain amyloidosis (AL) at the time of diagnostic bone marrow biopsy in newly diagnosed patients with multiple myeloma and smoldering myeloma. A series of 144 cases and a review of the literature | Q37774301 | ||
Molecular imaging of amyloidosis: will the heart be the next target after the brain? | Q37970935 | ||
Prognostication of survival using cardiac troponins and N-terminal pro-brain natriuretic peptide in patients with primary systemic amyloidosis undergoing peripheral blood stem cell transplantation | Q39128093 | ||
Serum uric acid: novel prognostic factor in primary systemic amyloidosis | Q40117481 | ||
Sustained improvement in cardiac function with persistent amyloid deposition in a patient with multiple myeloma-associated cardiac amyloidosis treated with bortezomib | Q42847216 | ||
Lenalidomide in combination with melphalan and dexamethasone in patients with newly diagnosed AL amyloidosis: a multicenter phase 1/2 dose-escalation study | Q42931881 | ||
Cyclophosphamide-bortezomib-dexamethasone (CyBorD) produces rapid and complete hematologic response in patients with AL amyloidosis. | Q43050098 | ||
Bortezomib with or without dexamethasone in primary systemic (light chain) amyloidosis | Q43189700 | ||
Amyloid in bone marrow smears of patients affected by multiple myeloma | Q43247364 | ||
Thalidomide: a step forward in the treatment of malignant monoclonal gammopathies. | Q44388184 | ||
Trends in day 100 and 2-year survival after auto-SCT for AL amyloidosis: outcomes before and after 2006. | Q44468671 | ||
New criteria for response to treatment in immunoglobulin light chain amyloidosis based on free light chain measurement and cardiac biomarkers: impact on survival outcomes | Q44572498 | ||
End-stage renal failure due to amyloidosis: outcomes in 490 ANZDATA registry cases. | Q44907517 | ||
Ten-year survival after autologous stem cell transplantation for immunoglobulin light chain amyloidosis | Q44960748 | ||
Long-term outcomes of patients with light chain amyloidosis (AL) after renal transplantation with or without stem cell transplantation | Q45896840 | ||
Treatment of patients with advanced cardiac AL amyloidosis with oral melphalan, dexamethasone, and thalidomide | Q46380099 | ||
Nodular senile pulmonary amyloidosis: a unique case confirmed by immunohistochemistry, mass spectrometry, and genetic study | Q46764637 | ||
Efficacy of bortezomib in systemic AL amyloidosis with relapsed/refractory clonal disease | Q46775156 | ||
Bortezomib in the treatment of AL amyloidosis: targeted therapy? | Q46892406 | ||
Amyloid load in fat tissue reflects disease severity and predicts survival in amyloidosis | Q46904469 | ||
Serum free light chain analysis may miss monoclonal light chains that urine immunofixation electrophoreses would detect | Q47895749 | ||
Glycosaminoglycans are part of amyloid fibrils: ultrastructural evidence in avian AA amyloid stained with cuprolinic blue and labeled with immunogold. | Q50479496 | ||
Reliable typing of systemic amyloidoses through proteomic analysis of subcutaneous adipose tissue. | Q50526227 | ||
Prevalence and origin of amyloid in kidney biopsies. | Q50604623 | ||
Treatment of 100 patients with primary amyloidosis: a randomized trial of melphalan, prednisone, and colchicine versus colchicine only. | Q51033339 | ||
Seeking confidence in the diagnosis of systemic AL (Ig light-chain) amyloidosis: patients can have both monoclonal gammopathies and hereditary amyloid proteins. | Q51954022 | ||
Amyloid in endomyocardial biopsies. | Q52904497 | ||
Prognostic significance of strain Doppler imaging in light-chain amyloidosis. | Q53066780 | ||
Troponin T level as an exclusion criterion for stem cell transplantation in light-chain amyloidosis. | Q53504425 | ||
Living donor kidney and autologous stem cell transplantation for primary systemic amyloidosis (AL) with predominant renal involvement. | Q53671959 | ||
Treatment of "primary" renal amyloidosis with melphalan. | Q54196552 | ||
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A phase 1/2 study of lenalidomide with low-dose oral cyclophosphamide and low-dose dexamethasone (RdC) in AL amyloidosis | Q57904446 | ||
Cardiac changes in systemic amyloidosis: Visualisation by magnetic resonance imaging | Q58009561 | ||
Salvage therapy with lenalidomide and dexamethasone in patients with advanced AL amyloidosis refractory to melphalan, bortezomib, and thalidomide | Q58030111 | ||
Identification of Amyloidogenic Light Chains Requires the Combination of Serum-Free Light Chain Assay with Immunofixation of Serum and Urine | Q58030328 | ||
Treatment with oral melphalan plus dexamethasone produces long-term remissions in AL amyloidosis | Q58030485 | ||
Renal Transplantation in Systemic Amyloidosis-Importance of Amyloid Fibril Type and Precursor Protein Abundance | Q58853072 | ||
Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survival | Q58853078 | ||
Outcome in Renal AL Amyloidosis After Chemotherapy | Q58853111 | ||
High-Dose Melphalan versus Melphalan plus Dexamethasone for AL Amyloidosis | Q58853165 | ||
Safety and efficacy of risk-adapted cyclophosphamide, thalidomide, and dexamethasone in systemic AL amyloidosis | Q58853178 | ||
Autologous stem cell transplant for immunoglobulin light chain amyloidosis: a status report | Q60976607 | ||
High-Dose Chemotherapy with Autotransplantation in AL Amyloidosis: A Flawed Meta-analysis | Q60976621 | ||
Effect of hematologic response on outcome of patients undergoing transplantation for primary amyloidosis: importance of achieving a complete response | Q60976697 | ||
A second course of high-dose melphalan and auto-SCT for the treatment of relapsed AL amyloidosis | Q63413669 | ||
A trial of three regimens for primary amyloidosis: colchicine alone, melphalan and prednisone, and melphalan, prednisone, and colchicine | Q73247899 | ||
Classification of amyloidosis: misdiagnosing by way of incomplete immunohistochemistry and how to prevent it | Q79765776 | ||
Predictors of survival in patients with systemic light-chain amyloidosis and cardiac involvement initially ineligible for stem cell transplantation and treated with oral melphalan and dexamethasone | Q81762674 | ||
Left ventricular hypertrophy: cardiac magnetic resonance may help differentiate amyloidosis from hypertrophic cardiomyopathy | Q82831169 | ||
Primary localized cutaneous amyloidosis: a sign of immune dysregulation? | Q83589494 | ||
Treatment with intravenous melphalan and dexamethasone is not able to overcome the poor prognosis of patients with newly diagnosed systemic light chain amyloidosis and severe cardiac involvement | Q84019269 | ||
Bladder amyloidosis | Q84077354 | ||
I don't know how to treat amyloidosis | Q84617604 | ||
Efficacy of the combination of bortezomib and dexamethasone in systemic AL amyloidosis | Q84990268 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 416-25 | |
P577 | publication date | 2013-05-01 | |
P1433 | published in | American Journal of Hematology | Q4744246 |
P1476 | title | Immunoglobulin light chain amyloidosis: 2013 update on diagnosis, prognosis, and treatment | |
P478 | volume | 88 |
Q58087715 | Amyloidosis of the Upper Aerodigestive Tract: Management of a Rare Disease and Review of the Literature |
Q40918755 | Bortezomib with dexamethasone as first-line treatment for AL amyloidosis with renal involvement |
Q35834954 | Clinical features and outcomes of systemic amyloidosis with gastrointestinal involvement: a single-center experience |
Q41448448 | Clinicopathological features of renal amyloidosis: a single-center study on 47 cases |
Q40979010 | Combination of lenalidomide and low-dose dexamethasone therapy promotes the anticoagulant activity of warfarin in patients with immunoglobulin light-chain amyloidosis |
Q38172998 | Future directions in the clinical management of amyloid light-chain amyloidosis |
Q93052569 | Immunoglobulin Light Chain Amyloidosis with Severe Liver Dysfunction Accompanied by Factor X Deficiency |
Q35081363 | Induction therapy with bortezomib and dexamethasone followed by autologous stem cell transplantation versus autologous stem cell transplantation alone in the treatment of renal AL amyloidosis: a randomized controlled trial |
Q35820992 | Insight into the Protein Composition of Immunoglobulin Light Chain Deposits of Eyelid, Orbital and Conjunctival Amyloidosis. |
Q36862056 | Isolated intracerebral light chain deposition disease: novel imaging and pathologic findings |
Q36384308 | Laryngeal amyloidosis: diagnosis, pathophysiology and management |
Q38556941 | Light Chain (AL) Amyloidosis: The Journey to Diagnosis |
Q45870533 | Light-chain amyloidosis presenting as a change in bleeding phenotype in a patient with mild haemophilia A. |
Q89800743 | Light-chain and transthyretin cardiac amyloidosis in severe aortic stenosis: prevalence, screening possibilities, and outcome |
Q41575087 | Localized amyloidosis of the upper gingiva: a case report |
Q37035201 | Long term outcomes of cardiac transplant for immunoglobulin light chain amyloidosis: The Mayo Clinic experience |
Q37570615 | Long-term event-free and overall survival after risk-adapted melphalan and SCT for systemic light chain amyloidosis |
Q35156344 | Mid-infrared free-electron laser tuned to the amide I band for converting insoluble amyloid-like protein fibrils into the soluble monomeric form |
Q64105650 | Multiorgan involvement by amyloid light chain amyloidosis |
Q38250214 | Neuroarthropathy of the foot revealing primary systemic amyloidosis: case report and literature review. |
Q38259728 | Pathophysiology and treatment of cardiac amyloidosis |
Q47160869 | Psychometric validation of the SF-36 Health Survey in light chain amyloidosis: results from community-based and clinic-based samples |
Q37593524 | The burden of amyloid light chain amyloidosis on health-related quality of life |
Q35026460 | The clinical features and outcomes of systemic AL amyloidosis: a cohort of 231 Chinese patients |
Q47228766 | The long-term Outcomes after VAD plus SCT Therapy in a Patient with AL Amyloidosis and Severe Factor X Deficiency |
Q37375492 | Thermal stability threshold for amyloid formation in light chain amyloidosis |
Q41046690 | Transthyretin amyloid neuropathy has earlier neural involvement but better prognosis than primary amyloid counterpart: an answer to the paradox? |
Q52981600 | Treatment of hepatic amyloid light-chain amyloidosis with bortezomib and dexamethasone in a liver transplant patient. |
Q38759595 | siRNA targeting the κ light chain constant region: preclinical testing of an approach to nonfibrillar and fibrillar light chain deposition diseases |
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