Differentiating Creatine and Phosphocreatine In Vivo Using <scp> 3 T <sup>1</sup> H MR </scp> Spectroscopy
Without prior knowledge of the non-metabolite signal, default settings of LCModel can introduce significant bias. Modified setup for LCModel improves quantitation of phosphocreatine and reduces bias in the overall set of metabolites.
Authors
- Frank L. Hanley
- Philip M. Adamson (ORCID: https://orcid.org/0000-0002-5028-0683)
- Moussa Haidar (ORCID: https://orcid.org/0000-0001-6369-7616)
- Kenichi Okamura (ORCID: https://orcid.org/0000-0001-9205-3457)
- R. Kirk Riemer (ORCID: https://orcid.org/0000-0002-3054-9809)
- Daniel M. Spielman (ORCID: https://orcid.org/0000-0003-0838-6967)
- Yoshikazu Ono (ORCID: https://orcid.org/0009-0008-8041-5164)
- Masafumi Shibata (ORCID: https://orcid.org/0000-0001-8543-1317)
- Meng Gu
- Ralph E. Hurd (ORCID: https://orcid.org/0009-0000-7523-685X)
Institutions
- Stanford Medicine (US)
- Stanford University (US)
Publication Details
- Journal
- Magnetic Resonance in Medicine
- Published
- 2025-11-09
- DOI
- https://doi.org/10.1002/mrm.70171
- Primary Topic
- Advanced MRI Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00