专题:Amyloidosis: Diagnosis, Treatment, Outcomes

This cluster of papers focuses on the molecular mechanisms, diagnosis, treatment, and prognosis of amyloidosis, with a particular emphasis on transthyretin-related cardiac and familial amyloid polyneuropathy. It covers topics such as RNAi therapy, cardiovascular magnetic resonance, and immunoglobulin light chain involvement.
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Amyloid PET Burden, CSF Biomarkers, and APOE Genotype in People With Iatrogenic and Sporadic Cerebral Amyloid Angiopathy

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Clinical implications beyond radiological findings in hypothalamic–pituitary neurosarcoidosis: A commentary

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Cardiac Biomarker Complete Response in AL Amyloidosis

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Visceral technetium-99 m-labeled pyrophosphate uptake in patients with wild-type transthyretin cardiac amyloidosis

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Severe Hypertension and Hematologic Abnormalities in Pseudoxanthoma Elasticum: A Pediatric Case Report

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Teriparatide in Two Patients With Mucopolysaccharidosis Type IVB

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Neuropsychiatric Manifestations of Acitretin-Induced Hyperhomocysteinemia in a Patient With Chronic Plaque Psoriasis

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Kinetics of Technetium-Labeled Cardiac Amyloid Radionuclide Imaging

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Cascade genetic screening in families with hereditary transthyretin amyloidosis: diagnostic and prognostic impact

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Sodium-Glucose Cotransporter-2 Inhibitors Therapy in Transthyretin Amyloid Cardiomyopathy: A Propensity-Matched Cohort Study

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