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Editorial
. 2023 Feb;67(2):98-100.
doi: 10.1002/mus.27754. Epub 2022 Nov 27.

Skeletal muscle 99mTechnetium-pyrophosphate scan: More questions than answers

Marcus V Pinto  1 , Teerin Liewluck  1
Affiliations
Editorial

Skeletal muscle 99mTechnetium-pyrophosphate scan: More questions than answers

Marcus V Pinto et al. Muscle Nerve. 2023 Feb.
No abstract available

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References

REFERENCES

    1. Pinto MV, Dyck PJB, Liewluck T. Neuromuscular amyloidosis: unmasking the master of disguise. Muscle Nerve. 2021;64(1):23-36.
    1. Adams D, Koike H, Slama M, Coelho T. Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease. Nat Rev Neurol. 2019;15(7):387-404.
    1. Ruberg FL, Grogan M, Hanna M, Kelly JW, Maurer MS. Transthyretin amyloid cardiomyopathy: JACC state-of-the-art review. J Am Coll Cardiol. 2019;73(22):2872-2891.
    1. Pinto MV, Milone M, Mauermann ML, et al. Transthyretin amyloidosis: putting myopathy on the map. Muscle Nerve. 2020;61(1):95-100.
    1. Hanna M, Ruberg FL, Maurer MS, et al. Cardiac scintigraphy with technetium-99m-labeled bone-seeking tracers for suspected amyloidosis: JACC review topic of the week. J Am Coll Cardiol. 2020;75(22):2851-2862.

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