Studies
Assessing Neural Mechanisms using MRI and Magnetic Resonance Spectroscopy
Assessing Neural Mechanisms using MRI and Magnetic Resonance Spectroscopy
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Overview
Selected Publications (10)
Neurological implications of urea cycle disorders
A. Gropman, Marshall L. Summar, J. Leonard. (2007). Journal of Inherited Metabolic Disease. Cited 211 times.
https://doi.org/10.1007/s10545-007-0709-5
Brain imaging in urea cycle disorders.
A. Gropman. (2010). Molecular genetics and metabolism. Cited 78 times.
https://doi.org/10.1016/j.ymgme.2010.01.017
1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.
A. Gropman, S. Fricke, S. Fricke, et al.. (2008). Molecular genetics and metabolism. Cited 50 times.
https://doi.org/10.1016/j.ymgme.2008.06.003
Diffusion Tensor Imaging Detects Areas of Abnormal White Matter Microstructure in Patients with Partial Ornithine Transcarbamylase Deficiency
A. Gropman, B. Gertz, K. Shattuck, et al.. (2010). American Journal of Neuroradiology. Cited 35 times.
https://doi.org/10.3174/ajnr.A2122
Patterns of brain injury in inborn errors of metabolism.
A. Gropman. (2012). Seminars in pediatric neurology. Cited 30 times.
https://doi.org/10.1016/j.spen.2012.09.007
Altered neural activation in ornithine transcarbamylase deficiency during executive cognition: An fMRI study
A. Gropman, K. Shattuck, M. Prust, et al.. (2013). Human Brain Mapping. Cited 27 times.
https://doi.org/10.1002/hbm.21470
Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts.
Michael S Oldham, J. VanMeter, K. Shattuck, et al.. (2010). Pediatric neurology. Cited 26 times.
https://doi.org/10.1016/j.pediatrneurol.2009.07.017
1H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations.
A. Gropman, R. Seltzer, M. Yudkoff, et al.. (2008). Molecular genetics and metabolism. Cited 21 times.
https://doi.org/10.1016/j.ymgme.2007.12.008
Urea cycle defects and hyperammonemia: effects on functional imaging
A. Gropman, M. Prust, A. Breeden, et al.. (2012). Metabolic Brain Disease. Cited 20 times.
https://doi.org/10.1007/s11011-012-9348-0
New frontiers in neuroimaging applications to inborn errors of metabolism.
M. Prust, A. Gropman, N. Hauser. (2011). Molecular genetics and metabolism. Cited 11 times.
https://doi.org/10.1016/j.ymgme.2011.06.020
