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JACC. Case Reports|September 17, 2026
Pneumococcal Mitral Endocarditis Unmasking Austrian SyndromeIvan R Figueroa Baez, Angel Davila, Marcos Fernandez, et al.
JACC. Case Reports|September 25, 2026
Myocarditis-Like Presentation Leads to DSP Arrhythmogenic Cardiomyopathy Diagnosis: From Variant of Uncertain Significance to DiagnosisOlivia DeLorenzo, Farid Farkouh, Ibrahim Alameh, et al.
JACC. Case Reports|September 25, 2026
Intravascular Lithotripsy Balloon Entrapped in Right Coronary Artery Requiring Surgical BailoutPranev Sharma, Helen Routledge, Jasper Trevelyan
JACC. Case Reports|September 24, 2026
Sustained Ventricular Tachycardia as the First Presentation of Hereditary Transthyretin Amyloidosis With the Glu109Gln MutationThomas Weiss, Sie K Fensman, Astrid J Terkelsen, et al.
JACC. Case Reports|September 24, 2026
TTR Variant p.Ala65Val Causing Early-Onset Hereditary Transthyretin Amyloidosis With Mixed Cardiac and Neuropathic PhenotypeJavier Torres-Valencia, Sebastian Reyes-Villanes, Elder Quispe, et al.
JACC. Case Reports|September 24, 2026
Perugini Grade 3 Uptake Does Not Exclude AL Cardiac Amyloidosis: When Noninvasive Diagnosis FailsFulvio Cacciapuoti, Vittorio Taglialatela, Giuseppe Nicoletti, et al.
JACC. Case Reports|September 24, 2026
When Hematologic Response Does Not Translate to Cardiac Recovery in AL AmyloidosisPragyat Futela, Poornima Vinod, Bala Pushparaji, et al.
JACC. Case Reports|September 24, 2026
Hereditary Transthyretin Amyloidosis in Brazilian Amazon Caused by a Globally Rare Variant Predominant in AsiaMatheus Martins Monteiro, Marcela Oliveira de Azevedo, Rodrigo Fernandes de Castro, et al.
JACC. Case Reports|September 24, 2026
Multimodality Imaging Reveals Rare Hereditary Transthyretin Amyloidosis Mimicking Hypertrophic CardiomyopathyMaria Panelo, Yoel Tuya-Acosta, Adriana Soto-Priore, et al.
JACC. Case Reports|September 24, 2026
Epicardial Amyloidoma Mimicking Secondary Cardiac Lymphoma: A Sneeze Away From the DiagnosisAlessandro Vella, Giandomenico Disabato, Lucia Roncoroni, et al.
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