Tendons are highly ordered tissues, mainly composed of collagen, and characterized by very short transverse T2* relaxation times. Even when using ultra-short echo-time imaging sequences, quantification of T2* is challenging as the origin and characteristics of the signal decay in tendons is still under debate. In this work, we finely sampled the decay of the transverse magnetization using an echo-train shifted multi-echo ultra-short echo-time sequence with 55 echoes and applied a complex tri-exponential model to extract T2* constants.
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