Welcome to our SEPTEMBER 23 special sponsored issue of #JACCCaseReports @JACCJournals on cardiac #amyloidosis! jacc.org/journal/case-report…. Full PDF here: jacc.org/doi/10.1016/S2666-0… Thank you @JoshMitchellMD for being our guest Editor-in-Chief! Cardiac Amyloidosis: A Field Transformed and the Work That Remains jacc.org/doi/10.1016/j.jacca… @minnowalsh @hmkyale Imaging and Diagnostic Challenges and Pitfalls ATTR-CM in Patients With Clinically Significant Plasma Cell Dyscrasias: A Case Series Highlighting Diagnostic Challenges jacc.org/doi/10.1016/j.jacca… Donut Morphology of Cardiac Amyloidosis: A Glazed Over Diagnosis jacc.org/doi/10.1016/j.jacca… Systemic Oxalosis Mimicking Transthyretin Amyloid Cardiomyopathy: A Cause of False Positive Tc-99m PYP Scintigraphy jacc.org/doi/10.1016/j.jacca… Perugini Grade 3 Uptake Does Not Exclude AL Cardiac Amyloidosis: When Noninvasive Diagnosis Fails jacc.org/doi/10.1016/j.jacca… 3 Discordant Extracardiac Amyloid Proteins Highlighting Bystander Deposition in a Case of Light-Chain Amyloid Cardiomyopathy jacc.org/doi/10.1016/j.jacca… Successful Heart Transplantation in a Patient With Triple Infiltrative Cardiomyopathy: Sarcoidosis, AL and TTR Amyloidosis jacc.org/doi/10.1016/j.jacca… Abnormal Cardiac PET Imaging in ATTR Amyloidosis jacc.org/doi/10.1016/j.jacca… Early Recognition and Atypical Presenatations Epicardial Amyloidoma Mimicking Secondary Cardiac Lymphoma: A Sneeze Away From the Diagnosis jacc.org/doi/10.1016/j.jacca… Smartwatch-Detected Sinus Tachycardia Unmasking AL Cardiac Amyloidosis in a Young Adult jacc.org/doi/10.1016/j.jacca… Transthyretin Cardiac Amyloidosis in a Safety-Net Hospital: A Case Series of 10 Afro-Caribbean Patients jacc.org/doi/10.1016/j.jacca… Sustained Ventricular Tachycardia as the First Presentation of Hereditary Transthyretin Amyloidosis With the Glu109Gln Mutation jacc.org/doi/10.1016/j.jacca… Light Chain Cardiac Amyloidosis With Skeletal Muscle Weakness jacc.org/doi/10.1016/j.jacca… Amyloid Light Chain Amyloidosis Involving the Heart and Temporal Arteries, Mimicking Giant Cell Arteritis jacc.org/doi/10.1016/j.jacca… Obstructive Intramural Coronary Amyloidosis: Uncommon or Under-Recognized Cause of Microvascular Angina? jacc.org/doi/10.1016/j.jacca… p.(V142I)-Associated Variant Transthyretin Amyloid Cardiomyopathy Complicating Complex Congenital Heart Disease: A Lethal Combination jacc.org/doi/10.1016/j.jacca… Hypertrophic Cardiomyopathy Overlap Hereditary Transthyretin Cardiac Amyloidosis With Severe Left Ventricular Outflow Tract Obstruction Mimicking Hypertrophic Obstructive Cardiomyopathy jacc.org/doi/10.1016/j.jacca… Multimodality Imaging Reveals Rare Hereditary Transthyretin Amyloidosis Mimicking Hypertrophic Cardiomyopathy jacc.org/doi/10.1016/j.jacca… Unmasking AL Cardiac Amyloidosis During Familial Cardiomyopathy Screening jacc.org/doi/10.1016/j.jacca… Coexistence of Hypertrophic Cardiomyopathy and Hereditary Transthyretin Amyloid Cardiomyopathy jacc.org/doi/10.1016/j.jacca… Management and Hemodynamics Abnormal Cardiovascular Responses During Orthostatic Hypotension in Cardiac Amyloidosis Revealed by Semi-Sitting/Standing Stress Echocardiography jacc.org/doi/10.1016/j.jacca… Neurohormonal Therapy in Patients With Transthyretin Cardiac Amyloidosis: Is It an Option? jacc.org/doi/10.1016/j.jacca… Early Recovery of Cardiac Function After Hematologic Response in Systemic AL Amyloidosis jacc.org/doi/10.1016/j.jacca… When Hematologic Response Does Not Translate to Cardiac Recovery in AL Amyloidosis jacc.org/doi/10.1016/j.jacca… Rare Amyloid Types and Genetic ATTR Variant’s Page Apolipoprotein A-IV Cardiac Amyloidosis: Beyond ATTR and AL jacc.org/doi/10.1016/j.jacca… Apolipoprotein A-IV Cardiac Amyloidosis Presenting as Massive Ventricular Wall Thickening Mimicking Hypertrophic Cardiomyopathy jacc.org/doi/10.1016/j.jacca… Apolipoprotein A-IV Cardiac Amyloidosis as a Diagnostic Pitfall: Beyond the Noninvasive Algorithm jacc.org/doi/10.1016/j.jacca… Transthyretin Amyloidosis Due to a Rare TTR Val142del Deletion With Relatively Early Clinical Manifestations jacc.org/doi/10.1016/j.jacca… TTR Variant p.Ala65Val Causing Early-Onset Hereditary Transthyretin Amyloidosis With Mixed Cardiac and Neuropathic Phenotype jacc.org/doi/10.1016/j.jacca… Rare Hereditary Cardiac Amyloidosis Treated With SGLT2 Inhibitor: Beyond ATTR/AL jacc.org/doi/10.1016/j.jacca… Hereditary Transthyretin Amyloidosis in Brazilian Amazon Caused by a Globally Rare Variant Predominant in Asia jacc.org/doi/10.1016/j.jacca… @NAkhterMD @aroniskn @CraigBasman @JACabreraCardio @MiChen__ @aabha_divya @MarcEngels7 @sarano_maurice @Miho_Fukui_ @CardioOncCO @MMarinCuartas @Nishaki1 @ChrissyMD2000 @ACHDocTMoe @PanjrathG @jsaef1 @Kentso987 @TagliariPaula @m_taramasso @SyedZaidMD