1M01RR020359-010058/RR/NCRR NIH HHS/United States[Grants and Funding] - Search Results

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2008	2
2012	1
2013	1
2025	0

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Urea cycle defects and hyperammonemia: effects on functional imaging.

Gropman AL, Prust M, Breeden A, Fricke S, VanMeter J. Gropman AL, et al. Metab Brain Dis. 2013 Jun;28(2):269-75. doi: 10.1007/s11011-012-9348-0. Epub 2012 Nov 13. Metab Brain Dis. 2013. PMID: 23149878 Free PMC article.

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Gropman AL, Fricke ST, Seltzer RR, Hailu A, Adeyemo A, Sawyer A, van Meter J, Gaillard WD, McCarter R, Tuchman M, Batshaw M; Urea Cycle Disorders Consortium. Gropman AL, et al. Mol Genet Metab. 2008 Sep-Oct;95(1-2):21-30. doi: 10.1016/j.ymgme.2008.06.003. Epub 2008 Jul 26. Mol Genet Metab. 2008. PMID: 18662894 Free PMC article.

1H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations.

Gropman AL, Seltzer RR, Yudkoff M, Sawyer A, VanMeter J, Fricke ST. Gropman AL, et al. Mol Genet Metab. 2008 May;94(1):52-60. doi: 10.1016/j.ymgme.2007.12.008. Epub 2008 Feb 11. Mol Genet Metab. 2008. PMID: 18262815 Free PMC article.

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