Cardiac Amyloid - An Update

scientific article published on 01 December 2015

Cardiac Amyloid - An Update is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.15420/ECR.2015.10.2.113
P932PMC publication ID6159448
P698PubMed publication ID30310435

P2093author name stringJason N Dungu
P2860cites workUpdate on treatment of light chain amyloidosisQ26829735
Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosisQ28217930
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trialQ28304712
Transthyretin Amyloidosis: Chaperone Concentration Changes and Increased Proteolysis in the Pathway to DiseaseQ28546193
Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimensQ33508070
Antibodies to human serum amyloid P component eliminate visceral amyloid depositsQ34144814
Primary systemic amyloidosis: clinical and laboratory features in 474 cases.Q34320169
Senile systemic amyloidosis: clinical features at presentation and outcomeQ34340740
Novel drugs targeting transthyretin amyloidosisQ34400138
Could late enhancement and need for permanent pacemaker implantation in patients undergoing TAVR be explained by undiagnosed transthyretin cardiac amyloidosis?Q53637234
Isolation and characterization of amyloid fibrils from tissue.Q53706819
Defining the diagnosis in echocardiographically suspected senile systemic amyloidosis.Q53772437
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosisQ55670644
Tabulation of human transthyretin (TTR) variants, 2003Q58011075
CMR-Based Differentiation of AL and ATTR Cardiac AmyloidosisQ58853065
Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survivalQ58853078
Correlation of histomorphological pattern of cardiac amyloid deposition with amyloid type: a histological and proteomic analysis of 108 casesQ60976358
Utility and limitations of 3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in systemic amyloidosisQ61657843
Coexistence of Degenerative Aortic Stenosis and Wild-Type Transthyretin-Related Cardiac AmyloidosisQ62083154
Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlationQ64361284
Sensitivity and specificity of the echocardiographic features of cardiac amyloidosisQ70023104
The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvementQ74524530
Cardiovascular magnetic resonance in clinically suspected cardiac amyloidosis: noninvasive imaging compared to endomyocardial biopsyQ80833658
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 dexamethasoneQ81762674
Unveiling wild-type transthyretin cardiac amyloidosis as a significant and potentially modifiable cause of heart failure with preserved ejection fractionQ85674220
Usefulness of Combining Electrocardiographic and Echocardiographic Findings and Brain Natriuretic Peptide in Early Detection of Cardiac Amyloidosis in Subjects With Transthyretin Gene MutationQ85856496
Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black AmericansQ34415207
Therapeutic Clearance of Amyloid by Antibodies to Serum Amyloid P ComponentQ34485172
Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fractionQ34487487
Prevalence of monoclonal gammopathy of undetermined significanceQ34506801
Therapeutic strategies for human amyloid diseasesQ34743288
T1 mapping and survival in systemic light-chain amyloidosisQ34994098
The amyloidogenic V122I transthyretin variant in elderly black AmericansQ35242225
Light Chain Amyloid Fibrils Cause Metabolic Dysfunction in Human CardiomyocytesQ35783283
Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosisQ35886289
A novel mechano-enzymatic cleavage mechanism underlies transthyretin amyloidogenesisQ36159473
Prognostic Value of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Cardiac AmyloidosisQ36165179
Extracellular volume quantification by dynamic equilibrium cardiac computed tomography in cardiac amyloidosisQ36384508
Evaluation and management of the cardiac amyloidosis.Q37013270
Diflunisal for ATTR cardiac amyloidosisQ37055082
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathyQ37301237
Amyloid diseases of the heart: assessment, diagnosis, and referralQ37819545
The transthyretin amyloidoses: from delineating the molecular mechanism of aggregation linked to pathology to a regulatory-agency-approved drugQ37975816
Cardiac transthyretin amyloidosis.Q38034215
Outcomes after heart transplantation for amyloid cardiomyopathy in the modern era.Q38343098
Differential Myocyte Responses in Patients with Cardiac Transthyretin Amyloidosis and Light-Chain Amyloidosis: A Cardiac MR Imaging StudyQ38425844
Native T1 mapping in transthyretin amyloidosisQ38442488
Cardiovascular magnetic resonance in cardiac amyloidosisQ38515487
Noninvasive Identification of ATTRwt Cardiac Amyloid: The Re-emergence of Nuclear CardiologyQ38532386
Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathyQ40378952
Noninvasive etiologic diagnosis of cardiac amyloidosis using 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphyQ40388294
Prevalence of the amyloidogenic transthyretin (TTR) V122I allele in 14 333 African-AmericansQ40784560
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II studyQ42646462
A new era in the treatment of amyloidosis?Q43961058
Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS).Q44545593
The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patientsQ46169582
V122I transthyretin variant in elderly black AmericansQ46206011
Revised transthyretin Ile 122 allele frequency in African-AmericansQ46220573
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy studyQ46645719
Safety and efficacy of RNAi therapy for transthyretin amyloidosisQ46836193
Role of cardiac magnetic resonance imaging in the detection of cardiac amyloidosisQ47861129
Clinical and echocardiographic characteristics for differentiating between transthyretin-related and light-chain cardiac amyloidosesQ48033249
Relative apical sparing of longitudinal strain using two-dimensional speckle-tracking echocardiography is both sensitive and specific for the diagnosis of cardiac amyloidosis.Q48771344
Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variantQ48847335
Relation of clinical, echocardiographic and electrocardiographic features of cardiac amyloidosis to the presence of the transthyretin V122I allele in older African-American men.Q48867075
Left ventricular structure and function in transthyretin-related versus light-chain cardiac amyloidosis.Q50622497
Prognostic significance of strain Doppler imaging in light-chain amyloidosis.Q53066780
P433issue2
P304page(s)113-117
P577publication date2015-12-01
P1433published inEuropean cardiologyQ27727460
P1476titleCardiac Amyloid - An Update
P478volume10

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