Moraitou M - Search Results

1

Circulating Brain-enriched MicroRNAs for detection and discrimination of idiopathic and genetic Parkinson's disease.

Ravanidis S, Bougea A, Papagiannakis N, Maniati M, Koros C, Simitsi AM, Bozi M, Pachi I, Stamelou M, Paraskevas GP, Kapaki E, Moraitou M, Michelakakis H, Stefanis L, Doxakis E. Ravanidis S, et al. Among authors: moraitou m. Mov Disord. 2020 Mar;35(3):457-467. doi: 10.1002/mds.27928. Epub 2019 Dec 4. Mov Disord. 2020. PMID: 31799764

2

The facile detection of 1505G-->A in Gaucher patients with different phenotypes.

Moraitou M, van Weely S, Verhoek M, Aerts J, Dimitriou E, Michelakakis H. Moraitou M, et al. Biochim Biophys Acta. 2001 May 31;1536(2-3):97-102. doi: 10.1016/s0925-4439(01)00033-3. Biochim Biophys Acta. 2001. PMID: 11406344 Free article.

3

Early-onset severe neurological involvement and D409H homozygosity in Gaucher disease: outcome of enzyme replacement therapy.

Michelakakis H, Skardoutsou A, Mathioudakis J, Moraitou M, Dimitriou E, Voudris C, Karpathios T. Michelakakis H, et al. Among authors: moraitou m. Blood Cells Mol Dis. 2002 Jan-Feb;28(1):1-4. doi: 10.1006/bcmd.2001.0477. Blood Cells Mol Dis. 2002. PMID: 11814305

4

PEX1 deficiency presenting as Leber congenital amaurosis.

Michelakakis HM, Zafeiriou DI, Moraitou MS, Gootjes J, Wanders RJ. Michelakakis HM, et al. Among authors: moraitou ms. Pediatr Neurol. 2004 Aug;31(2):146-9. doi: 10.1016/j.pediatrneurol.2004.01.013. Pediatr Neurol. 2004. PMID: 15301838

5

Elevated plasma chemokine CCL18/PARC in beta-thalassemia.

Dimitriou E, Verhoek M, Altun S, Karabatsos F, Moraitou M, Youssef J, Boot R, Sarafidou J, Karagiorga M, Aerts H, Michelakakis H. Dimitriou E, et al. Among authors: moraitou m. Blood Cells Mol Dis. 2005 Nov-Dec;35(3):328-31. doi: 10.1016/j.bcmd.2005.07.006. Epub 2005 Aug 31. Blood Cells Mol Dis. 2005. PMID: 16137900

6

Homozygosity for the double D409H+H255Q allele in type II Gaucher disease.

Michelakakis H, Moraitou M, Dimitriou E, Santamaria R, Sanchez G, Gort L, Chabas A, Grinberg D, Dassopoulou M, Fotopoulos S, Vilageliu L. Michelakakis H, et al. Among authors: moraitou m. J Inherit Metab Dis. 2006 Aug;29(4):591. doi: 10.1007/s10545-006-0316-x. Epub 2006 Jul 8. J Inherit Metab Dis. 2006. PMID: 16830265

7

Serum S100B levels in X-linked adrenoleukodystrophy and Gaucher disease.

Michelakakis H, Kariyannis C, Moraitou M, Dimitriou E, Sarafidou J, Papassotiriou I. Michelakakis H, et al. Among authors: moraitou m. J Inherit Metab Dis. 2007 Oct;30(5):822. doi: 10.1007/s10545-007-0640-9. Epub 2007 Aug 20. J Inherit Metab Dis. 2007. PMID: 17705023

8

Plasmalogen levels in Gaucher disease.

Moraitou M, Dimitriou E, Zafeiriou D, Reppa C, Marinakis T, Sarafidou J, Michelakakis H. Moraitou M, et al. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):196-9. doi: 10.1016/j.bcmd.2008.03.007. Epub 2008 May 23. Blood Cells Mol Dis. 2008. PMID: 18501647

9

Plasma lysosomal enzyme activities in congenital disorders of glycosylation, galactosemia and fructosemia.

Michelakakis H, Moraitou M, Mavridou I, Dimitriou E. Michelakakis H, et al. Among authors: moraitou m. Clin Chim Acta. 2009 Mar;401(1-2):81-3. doi: 10.1016/j.cca.2008.11.024. Epub 2008 Dec 3. Clin Chim Acta. 2009. PMID: 19100247

10

Plasmalogen levels in full-term neonates.

Labadaridis I, Moraitou M, Theodoraki M, Triantafyllidis G, Sarafidou J, Michelakakis H. Labadaridis I, et al. Among authors: moraitou m. Acta Paediatr. 2009 Apr;98(4):640-2. doi: 10.1111/j.1651-2227.2008.01205.x. Acta Paediatr. 2009. PMID: 19290965

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