What researchers published on Amiloidózis
1746 papers, newest first.
Showing 40 of 1746
Correction: Early neuro biomarker changes and electrophysiological nerve dysfunction in Swedish V50M hereditary transthyretin amyloidosis: a pilot study.Frontiers in neurology
Multimodal Validation and Disease Stage Dependency of ATTR Cardiomyopathy Red Flags in Patients With LV Thickening.ESC heart failure
ÁttekintésTransthyretin Amyloid Cardiomyopathy: Contemporary Pharmacological Management.European cardiology
Cardiovascular events and interventions in patients with light chain amyloidosis: a real-world study in the United States.BMC cardiovascular disorders
High efficacy and tolerability of daratumumab-based regimens in first-line treatment of patients with immunoglobulin light-chain amyloidosis: a real-world evidence analysis.Frontiers in immunology
CORRIGENDUM: Discontinuation of Tafamidis in Wild-Type Transthyretin Amyloid Cardiomyopathy Patients.Circulation reports
Use of contemporary cardiometabolic therapies in cardiac amyloidosis treated with tafamidis: A real-world propensity-matched analysis.Archives of cardiovascular diseases
Esetismertetés[Case report: choroidopathy associated with familial amyloidosis, Finnish type].[Zhonghua yan ke za zhi] Chinese journal of ophthalmology
EsetismertetésLight-chain amyloidosis causing left ventricular outflow tract obstruction managed with a dual-chamber pacemaker: a case report.European heart journal. Case reports
Two Cases of Lung Nodules Presenting With Kappa Light Chain Deposition Disease/Congo-Red Negative AL Amyloidosis.Case reports in pathology
Impact of daratumumab on stem cell collection in patients with AL amyloidosis.BMC cancer
ÁttekintésCardiac amyloidosis: the role of multimodality imaging.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
EsetismertetésTwo young women with severe Danon disease initially suspected to have cardiac amyloidosis: a case report and literature review.Frontiers in cardiovascular medicine
ÁttekintésTransforming cardiac amyloidosis care: navigating the evolving diagnostic and therapeutic landscape.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Artificial Intelligence Detects Cardiac Amyloidosis Before Clinical Diagnosis.Journal of cardiac failure
Rethinking the comprehensive management of transthyretin amyloid cardiomyopathy (ATTR-CM).Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Patients with AL cardiac amyloidosis report lower life satisfaction and social support than patients with transthyretin amyloidosis.European journal of cardiovascular nursing
A Validated Transthyretin Amyloid Cardiomyopathy Claims-Based Coding Algorithm: ValidATTR-US.Cardiology and therapy
White Blood Cell Count Is Associated With Hospitalisation for Heart Failure in Patients With ATTR Cardiac Amyloidosis.Clinical cardiology
Reassessment of TTR H88N from a Variant of Uncertain Significance to a Likely Pathogenic Variant Based on Phenotype-Specific Evidence in Hereditary Transthyretin Amyloidosis.Annals of laboratory medicine
Teaching NeuroImage: Gelsolin Amyloidosis: A Cause of Familial Progressive Facial and Bulbar Palsy.Neurology
ÁttekintésArrhythmia management in transthyretin amyloid cardiomyopathy.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Longitudinal changes in gastrointestinal amyloid deposition before and after patisiran treatment in Hereditary ATTR amyloidosis.Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
EsetismertetésMultiorgan [18F]florbetapir PET/CT uptake in multiple myeloma-associated systemic AL amyloidosis: a case report.Medical oncology (Northwood, London, England)
ÁttekintésFamily screening and genetic testing in transthyretin cardiac amyloidosis : Changing (not only) variant transthyretin cardiac amyloidosis.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Effects of Eplontersen on Cardiac Structure and Function in Patients With Transthyretin Amyloidosis With Cardiomyopathy: Insights from the CARDIO-TTRansform Trial.Circulation
ÁttekintésThe spectrum of amyloid cardiovascular disease.Heart failure reviews
ÁttekintésComprehensive geriatric assessment and frailty in transthyretin amyloid cardiomyopathy: toward more individualized and appropriate care.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Cardiac involvement in systemic AA amyloidosis: Beyond a nephrocentric view.International journal of cardiology
Myocardial Responses to Eplontersen in Transthyretin Amyloid Cardiomyopathy: The CARDIO-TTRansform CMR study.Circulation
Amyloid nomenclature 2026: update, novel proteins, and discussion of intracellular aggregates and toxicity. Recommendations by the International Society of Amyloidosis Nomenclature Committee.Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Timing of Artificial Intelligence vs Human Identification of Cardiac Amyloidosis on Echocardiography.Journal of cardiac failure
Prevalence, clinical implications and prognostic impact of frailty and other geriatric conditions in patients with transthyretin amyloid cardiomyopathy.Revista espanola de cardiologia (English ed.)
Hereditary transthyretin amyloidosis in peripheral neuropathy: prevalence, clinical features, and neurology-based screening in non-endemic Japan.Frontiers in neurology
PreprintComputational alternative to cardiac biopsy in multiple myeloma: utilizing the shape of routine laboratory data for the classification of AL cardiac amyloidosis.bioRxiv : the preprint server for biology
Increased Left Ventricular Wall Thickness without Increased Mechanical Dispersion: A Distinguishing Feature of Transthyretin Amyloidosis Cardiomyopathy.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
EsetismertetésEndomyocardial biopsy after leadless pacemaker implantation in patient with suspected cardiac amyloidosis.Journal of cardiology cases
Characteristics and outcomes of implantable cardioverter defibrillator therapy in patients with cardiac amyloidosis.BMC cardiovascular disorders
Megfigyeléses vizsgálatThe early dFLC level after autologous stem cell transplantation can predict the long-term prognosis of in patients with light chain amyloidosis.Annals of hematology
EsetismertetésWhen rare meets routine: A case report of amyloid light-chain amyloidosis with multiorgan involvement in primary care.Malaysian family physician : the official journal of the Academy of Family Physicians of Malaysia