MR Spectroscopy and Spectroscopic Imaging: Comparing 3.0 T versus 1.5 T

2006 ◽  
Vol 16 (2) ◽  
pp. 269-283 ◽  
Author(s):  
Ulrike Dydak ◽  
Michael Schär
Keyword(s):  
Mr Spectroscopy ◽  
Spectroscopic Imaging ◽  
3.0 T

A comparative study of myo-inositol quantification using lcmodel at 1.5 T and 3.0 T with 3 D 1H proton spectroscopic imaging of the human brain

2004 ◽  
Vol 22 (4) ◽  
pp. 523-528 ◽  
Author(s):  
Radhika Srinivasan ◽  
Daniel Vigneron ◽  
Napapon Sailasuta ◽  
Ralph Hurd ◽  
Sarah Nelson
Keyword(s):  
Comparative Study ◽  
Human Brain ◽  
Spectroscopic Imaging ◽  
3.0 T

3.0 T Proton MR Spectroscopy

2004 ◽  
Vol 17 (6) ◽  
pp. 784-794
Author(s):  
T. Scarabino ◽  
F. Nemore ◽  
G.M. Giannatempo ◽  
A. Bertolino ◽  
M. Tosetti ◽  
...  
Keyword(s):  
Mr Spectroscopy ◽  
Proton Mr Spectroscopy ◽  
3.0 T

Hepatic lipid composition analysis using 3.0-T MR spectroscopy in a steatotic rat model

2012 ◽  
Vol 30 (1) ◽  
pp. 112-121 ◽  
Author(s):  
Jochem R. van Werven ◽  
Hendrik A. Marsman ◽  
Aart J. Nederveen ◽  
Fiebo J. ten Kate ◽  
Thomas M. van Gulik ◽  
...  
Keyword(s):  
Rat Model ◽  
Lipid Composition ◽  
Mr Spectroscopy ◽  
Composition Analysis ◽  
Hepatic Lipid ◽  
3.0 T

Are there differences in the biochemical profile of bilateral normal testes? A 3.0 T 1H‐MR spectroscopy study

Andrologia ◽  
2020 ◽  
Vol 52 (5) ◽  
Author(s):  
Athina C. Tsili ◽  
Loukas G. Astrakas ◽  
Nikolaos Sofikitis ◽  
Maria I. Argyropoulou
Keyword(s):  
Mr Spectroscopy ◽  
Biochemical Profile ◽  
Spectroscopy Study ◽  
1H Mr Spectroscopy ◽  
3.0 T

scholarly journals Proton MR Spectroscopic Imaging in Pelizaeus-Merzbacher Disease

2003 ◽  
Vol 16 (3) ◽  
pp. 449-450 ◽  
Author(s):  
F. Pizzini ◽  
A. Fatemi ◽  
P.B. Barker ◽  
H.W. Moser ◽  
S. Naidu ◽  
...  
Keyword(s):  
Mr Spectroscopy ◽  
Phenotypic Expression ◽  
Gene Mutations ◽  
Spectroscopic Imaging ◽  
Chromosome X ◽  
Pelizaeus Merzbacher Disease ◽  
Mr Spectroscopic Imaging

We describe the MR spectroscopy findings in three patients with Pelizaeus-Merzbacker disease, a rare leukodystrophy associated with mutations of the PLP gene on chromosome X. The patients studied had different PLP gene mutations and presented different metabolic patterns, indicating a different phenotypic expression of mutations of the same gene.

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