Similar articles for PMID: 17353334

Year	Number of Results
1994	1
1996	2
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2000	1
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2002	3
2003	4
2004	5
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2007	12
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2013	12
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2015	7
2016	4
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2018	3
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2020	8
2021	6
2022	11
2023	4
2024	0

1

Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy study.

Bianchi MC, Tosetti M, Battini R, Leuzzi V, Alessandri' MG, Carducci C, Antonozzi I, Cioni G. Bianchi MC, et al. AJNR Am J Neuroradiol. 2007 Mar;28(3):548-54. AJNR Am J Neuroradiol. 2007. PMID: 17353334 Free PMC article. Clinical Trial.

2

Is ATP elevated in patients with GAMT deficiency?

Renema WK, Kan HE, Heerschap A. Renema WK, et al. AJNR Am J Neuroradiol. 2008 Feb;29(2):214; author reply 214. doi: 10.3174/ajnr.A0803. Epub 2007 Nov 16. AJNR Am J Neuroradiol. 2008. PMID: 18024580 Free PMC article. No abstract available.

3

Guanidinoacetate and creatine plus creatinine assessment in physiologic fluids: an effective diagnostic tool for the biochemical diagnosis of arginine:glycine amidinotransferase and guanidinoacetate methyltransferase deficiencies.

Carducci C, Birarelli M, Leuzzi V, Carducci C, Battini R, Cioni G, Antonozzi I. Carducci C, et al. Clin Chem. 2002 Oct;48(10):1772-8. Clin Chem. 2002. PMID: 12324495

4

Creatine deficiency syndromes.

Schulze A. Schulze A. Mol Cell Biochem. 2003 Feb;244(1-2):143-50. Mol Cell Biochem. 2003. PMID: 12701824 Review.

5

AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.

Braissant O, Henry H. Braissant O, et al. J Inherit Metab Dis. 2008 Apr;31(2):230-9. doi: 10.1007/s10545-008-0826-9. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392746 Free article. Review.

6

Magnetic resonance imaging reveals specific anatomical changes in the brain of Agat- and Gamt-mice attributed to creatine depletion and guanidinoacetate alteration.

Sinha A, Ahmed S, George C, Tsagaris M, Naufer A, von Both I, Tkachyova I, van Eede M, Henkelman M, Schulze A. Sinha A, et al. J Inherit Metab Dis. 2020 Jul;43(4):827-842. doi: 10.1002/jimd.12215. Epub 2020 Jan 27. J Inherit Metab Dis. 2020. PMID: 31951021

7

[Creatine deficiency syndromes].

Cheillan D, Cognat S, Vandenberghe N, Des Portes V, Vianey-Saban C. Cheillan D, et al. Rev Neurol (Paris). 2005 Mar;161(3):284-9. doi: 10.1016/s0035-3787(05)85034-9. Rev Neurol (Paris). 2005. PMID: 15800449 Review. French.

8

Cerebral creatine deficiencies: a group of treatable intellectual developmental disorders.

Stockler-Ipsiroglu S, van Karnebeek CD. Stockler-Ipsiroglu S, et al. Semin Neurol. 2014 Jul;34(3):350-6. doi: 10.1055/s-0034-1386772. Epub 2014 Sep 5. Semin Neurol. 2014. PMID: 25192512 Review.

9

Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology.

Stockler S, Schutz PW, Salomons GS. Stockler S, et al. Subcell Biochem. 2007;46:149-66. doi: 10.1007/978-1-4020-6486-9_8. Subcell Biochem. 2007. PMID: 18652076 Review.

10

MR spectroscopy of muscle and brain in guanidinoacetate methyltransferase (GAMT)-deficient mice: validation of an animal model to study creatine deficiency.

Renema WK, Schmidt A, van Asten JJ, Oerlemans F, Ullrich K, Wieringa B, Isbrandt D, Heerschap A. Renema WK, et al. Magn Reson Med. 2003 Nov;50(5):936-43. doi: 10.1002/mrm.10627. Magn Reson Med. 2003. PMID: 14587004 Free article.

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