What researchers published on Amiloidózis
1750 papers, newest first.
Showing 60 of 1750
Effects of Interleukin-6 Dysregulation in a Mouse Model of Alzheimer's Disease: Unraveling Complexity Beyond Amyloidosis.Cells
Extent of myocardial deposition and its association with heart failure in ATTR amyloidosis: tomographic patterns of [99mTc]Tc-DPD uptake.Revista espanola de medicina nuclear e imagen molecular
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
Immunoglobulin Light Chain Repertoire and Mutation Landscape in AL Amyloidosis: A Combined Proteomic and Computational Study of Kappa and Lambda Deposits.ChemMedChem
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
Multicentre study of activity quantification methods for 99m-Tc-pyrophosphate SPECT/CT in cardiac amyloidosis.Physica medica : PM : an international journal devoted to the applications of physics to medicine and biology : official journal of the Italian Association of Biomedical Physics (AIFB)
Áttekintés[Diagnosis of amyloidosis].Therapeutische Umschau. Revue therapeutique
Áttekintés[Therapy of immunoglobulin light-chain amyloidosis - everything a general practitioner wants to know].Therapeutische Umschau. Revue therapeutique
The Effectiveness of Teclistamab in Patients With Relapsed/Refractory Light Chain Amyloidosis: A Multicenter Retrospective Study.British journal of hospital medicine (London, England : 2005)
Closing the Diagnostic Gap in Transthyretin Amyloid Cardiomyopathy.Journal of the American Heart Association
Ejection Fraction and Wall Thickness in Cardiac Amyloidosis: Is It Time to Look Beyond Numbers That Are in Our "Comfort Zone"?JACC. Asia
[The AMY-Way project: enhancing the diagnostic pathway and expanding care capacity in the management of transthyretin amyloidosis in Italy. A multidisciplinary expert opinion.].Recenti progressi in medicina
Delays From Clinical Manifestations to Diagnosis of Transthyretin Amyloid Cardiomyopathy: A National Retrospective Cohort Study.Journal of the American Heart Association
Áttekintés[Symptomatic treatment of cardiac transthyretin amyloidosis].Therapeutische Umschau. Revue therapeutique
Áttekintés[Similarities and differences in the pathophysiology and epidemiology of systemic amyloidoses Focus on immunoglobulin light-chain amyloidosis, hereditary transthyretin amyloidosis and wild-type transthyretin amyloidosis].Therapeutische Umschau. Revue therapeutique
Intravenous daratumumab-based regimens for light-chain amyloidosis with kidney involvement: a retrospective real-world comparative study.BMC nephrology
Prevalence of Transthyretin Amyloidosis Among Older Taiwanese Patients With Heart Failure With Preserved Ejection Fraction: The PATCH-HFpEF Study.JACC. Asia
One-minute heart rate recovery and clinical outcomes in transthyretin cardiac amyloidosis: incremental model fit beyond conventional CPET indices.European heart journal open
Áttekintés[Amyloidosis in the current context - an interdisciplinary challenge].Therapeutische Umschau. Revue therapeutique
Hereditary ATTR amyloidosis in Italy: pathogenic variant patterns and clinical profiles from a multicenter genetic dataset.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Áttekintés[Specific treatment of transthyretin amyloid cardiomyopathy: established disease-modifying agents and emerging mechanisms].Therapeutische Umschau. Revue therapeutique
Left Atrial Strain and Left Atrio-Ventricular Coupling in Heart Failure Patients with Left Ventricular Hypertrophy and Wild-Type Transthyretin Cardiac Amyloidosis.Echocardiography (Mount Kisco, N.Y.)