scholarly article | Q13442814 |
P2093 | author name string | Jason N Dungu | |
P2860 | cites work | Update on treatment of light chain amyloidosis | Q26829735 |
Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis | Q28217930 | ||
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial | Q28304712 | ||
Transthyretin Amyloidosis: Chaperone Concentration Changes and Increased Proteolysis in the Pathway to Disease | Q28546193 | ||
Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimens | Q33508070 | ||
Antibodies to human serum amyloid P component eliminate visceral amyloid deposits | Q34144814 | ||
Primary systemic amyloidosis: clinical and laboratory features in 474 cases. | Q34320169 | ||
Senile systemic amyloidosis: clinical features at presentation and outcome | Q34340740 | ||
Novel drugs targeting transthyretin amyloidosis | Q34400138 | ||
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) amyloidosis | Q55670644 | ||
Tabulation of human transthyretin (TTR) variants, 2003 | Q58011075 | ||
CMR-Based Differentiation of AL and ATTR Cardiac Amyloidosis | Q58853065 | ||
Cyclophosphamide, bortezomib, and dexamethasone therapy in AL amyloidosis is associated with high clonal response rates and prolonged progression-free survival | Q58853078 | ||
Correlation of histomorphological pattern of cardiac amyloid deposition with amyloid type: a histological and proteomic analysis of 108 cases | Q60976358 | ||
Utility and limitations of 3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy in systemic amyloidosis | Q61657843 | ||
Coexistence of Degenerative Aortic Stenosis and Wild-Type Transthyretin-Related Cardiac Amyloidosis | Q62083154 | ||
Frequency and distribution of senile cardiovascular amyloid. A clinicopathologic correlation | Q64361284 | ||
Sensitivity and specificity of the echocardiographic features of cardiac amyloidosis | Q70023104 | ||
The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement | Q74524530 | ||
Cardiovascular magnetic resonance in clinically suspected cardiac amyloidosis: noninvasive imaging compared to endomyocardial biopsy | Q80833658 | ||
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 | ||
Unveiling wild-type transthyretin cardiac amyloidosis as a significant and potentially modifiable cause of heart failure with preserved ejection fraction | Q85674220 | ||
Usefulness of Combining Electrocardiographic and Echocardiographic Findings and Brain Natriuretic Peptide in Early Detection of Cardiac Amyloidosis in Subjects With Transthyretin Gene Mutation | Q85856496 | ||
Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans | Q34415207 | ||
Therapeutic Clearance of Amyloid by Antibodies to Serum Amyloid P Component | Q34485172 | ||
Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction | Q34487487 | ||
Prevalence of monoclonal gammopathy of undetermined significance | Q34506801 | ||
Therapeutic strategies for human amyloid diseases | Q34743288 | ||
T1 mapping and survival in systemic light-chain amyloidosis | Q34994098 | ||
The amyloidogenic V122I transthyretin variant in elderly black Americans | Q35242225 | ||
Light Chain Amyloid Fibrils Cause Metabolic Dysfunction in Human Cardiomyocytes | Q35783283 | ||
Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosis | Q35886289 | ||
A novel mechano-enzymatic cleavage mechanism underlies transthyretin amyloidogenesis | Q36159473 | ||
Prognostic Value of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Cardiac Amyloidosis | Q36165179 | ||
Extracellular volume quantification by dynamic equilibrium cardiac computed tomography in cardiac amyloidosis | Q36384508 | ||
Evaluation and management of the cardiac amyloidosis. | Q37013270 | ||
Diflunisal for ATTR cardiac amyloidosis | Q37055082 | ||
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy | Q37301237 | ||
Amyloid diseases of the heart: assessment, diagnosis, and referral | Q37819545 | ||
The transthyretin amyloidoses: from delineating the molecular mechanism of aggregation linked to pathology to a regulatory-agency-approved drug | Q37975816 | ||
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 Study | Q38425844 | ||
Native T1 mapping in transthyretin amyloidosis | Q38442488 | ||
Cardiovascular magnetic resonance in cardiac amyloidosis | Q38515487 | ||
Noninvasive Identification of ATTRwt Cardiac Amyloid: The Re-emergence of Nuclear Cardiology | Q38532386 | ||
Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy | Q40378952 | ||
Noninvasive etiologic diagnosis of cardiac amyloidosis using 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy | Q40388294 | ||
Prevalence of the amyloidogenic transthyretin (TTR) V122I allele in 14 333 African-Americans | Q40784560 | ||
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study | Q42646462 | ||
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 patients | Q46169582 | ||
V122I transthyretin variant in elderly black Americans | Q46206011 | ||
Revised transthyretin Ile 122 allele frequency in African-Americans | Q46220573 | ||
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study | Q46645719 | ||
Safety and efficacy of RNAi therapy for transthyretin amyloidosis | Q46836193 | ||
Role of cardiac magnetic resonance imaging in the detection of cardiac amyloidosis | Q47861129 | ||
Clinical and echocardiographic characteristics for differentiating between transthyretin-related and light-chain cardiac amyloidoses | Q48033249 | ||
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 variant | Q48847335 | ||
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 | ||
P433 | issue | 2 | |
P304 | page(s) | 113-117 | |
P577 | publication date | 2015-12-01 | |
P1433 | published in | European cardiology | Q27727460 |
P1476 | title | Cardiac Amyloid - An Update | |
P478 | volume | 10 |
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