scholarly journals In vivo hyperpolarized 13C MR spectroscopic imaging with 1H decoupling

2009 ◽  
Vol 197 (1) ◽  
pp. 100-106 ◽  
Author(s):  
Albert P. Chen ◽  
James Tropp ◽  
Ralph E. Hurd ◽  
Mark Van Criekinge ◽  
Lucas G. Carvajal ◽  
...  
2013 ◽  
Vol 229 ◽  
pp. 187-197 ◽  
Author(s):  
Sarah J. Nelson ◽  
Eugene Ozhinsky ◽  
Yan Li ◽  
Il woo Park ◽  
Jason Crane

NeuroImage ◽  
2012 ◽  
Vol 59 (1) ◽  
pp. 193-201 ◽  
Author(s):  
Myriam M. Chaumeil ◽  
Tomoko Ozawa ◽  
IlWoo Park ◽  
Kristen Scott ◽  
C. David James ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A116-A116
Author(s):  
H SCHLEMMER ◽  
T SAWATZKI ◽  
I DORNACHER ◽  
S SAMMET ◽  
M HELLENSCHMIDT ◽  
...  

1994 ◽  
Vol 31 (2) ◽  
pp. 185
Author(s):  
Yong Whee Bahk ◽  
Kyung Sub Shinn ◽  
Tae Suk Suh ◽  
Bo Young Choe ◽  
Kyo Ho Choi

Metabolites ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 504
Author(s):  
Seunggwi Park ◽  
Hashizume Rintaro ◽  
Seul Kee Kim ◽  
Ilwoo Park

The development of hyperpolarized carbon-13 (13C) metabolic MRI has enabled the sensitive and noninvasive assessment of real-time in vivo metabolism in tumors. Although several studies have explored the feasibility of using hyperpolarized 13C metabolic imaging for neuro-oncology applications, most of these studies utilized high-grade enhancing tumors, and little is known about hyperpolarized 13C metabolic features of a non-enhancing tumor. In this study, 13C MR spectroscopic imaging with hyperpolarized [1-13C]pyruvate was applied for the differential characterization of metabolic profiles between enhancing and non-enhancing gliomas using rodent models of glioblastoma and a diffuse midline glioma. Distinct metabolic profiles were found between the enhancing and non-enhancing tumors, as well as their contralateral normal-appearing brain tissues. The preliminary results from this study suggest that the characterization of metabolic patterns from hyperpolarized 13C imaging between non-enhancing and enhancing tumors may be beneficial not only for understanding distinct metabolic features between the two lesions, but also for providing a basis for understanding 13C metabolic processes in ongoing clinical trials with neuro-oncology patients using this technology.


2001 ◽  
Vol 120 (5) ◽  
pp. A116
Author(s):  
Heinz-Peter Schlemmer ◽  
Tanja Sawatzki ◽  
Ines Dornacher ◽  
Steffen Sammet ◽  
Michael Hellenschmidt ◽  
...  

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