Nicolaou P - Search Results

1

Charcot-Marie-Tooth disease in Cyprus: epidemiological, clinical and genetic characteristics.

Nicolaou P, Zamba-Papanicolaou E, Koutsou P, Kleopa KA, Georghiou A, Hadjigeorgiou G, Papadimitriou A, Kyriakides T, Christodoulou K. Nicolaou P, et al. Neuroepidemiology. 2010;35(3):171-7. doi: 10.1159/000314351. Epub 2010 Jun 23. Neuroepidemiology. 2010. PMID: 20571287

2

A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes.

Kleopa KA, Georgiou DM, Nicolaou P, Koutsou P, Papathanasiou E, Kyriakides T, Christodoulou K. Kleopa KA, et al. Among authors: nicolaou p. Neurogenetics. 2004 Sep;5(3):171-5. doi: 10.1007/s10048-004-0184-1. Epub 2004 Jun 17. Neurogenetics. 2004. PMID: 15205993

3

A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.

Georgiou DM, Nicolaou P, Chitayat D, Koutsou P, Babul-Hirji R, Vajsar J, Murphy J, Christodoulou K. Georgiou DM, et al. Among authors: nicolaou p. Can J Neurol Sci. 2006 Aug;33(3):311-6. doi: 10.1017/s0317167100005199. Can J Neurol Sci. 2006. PMID: 17001820

4

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia.

Nicolaou P, Georghiou A, Votsi C, Middleton LT, Zamba-Papanicolaou E, Christodoulou K. Nicolaou P, et al. BMC Med Genet. 2008 Apr 14;9:28. doi: 10.1186/1471-2350-9-28. BMC Med Genet. 2008. PMID: 18405395 Free PMC article.

5

A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.

Nicolaou P, Cianchetti C, Minaidou A, Marrosu G, Zamba-Papanicolaou E, Middleton L, Christodoulou K. Nicolaou P, et al. Eur J Hum Genet. 2013 Feb;21(2):190-4. doi: 10.1038/ejhg.2012.146. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781092 Free PMC article.

6

Genomic and genetic studies of systemic sclerosis: A systematic review.

Chairta P, Nicolaou P, Christodoulou K. Chairta P, et al. Among authors: nicolaou p. Hum Immunol. 2017 Feb;78(2):153-165. doi: 10.1016/j.humimm.2016.10.017. Epub 2016 Oct 29. Hum Immunol. 2017. PMID: 27984087 Review.

7

Deregulation of LRSAM1 expression impairs the levels of TSG101, UBE2N, VPS28, MDM2 and EGFR.

Minaidou A, Nicolaou P, Christodoulou K. Minaidou A, et al. Among authors: nicolaou p. PLoS One. 2019 Feb 6;14(2):e0211814. doi: 10.1371/journal.pone.0211814. eCollection 2019. PLoS One. 2019. PMID: 30726272 Free PMC article.

8

Genetic Susceptibility to Systemic Sclerosis in the Greek-Cypriot Population: A Pilot Study.

Chairta P, Psarelis S, Michailidou K, Demetriou C, Symeonidou S, Nicolaou P, Christodoulou K. Chairta P, et al. Among authors: nicolaou p. Genet Test Mol Biomarkers. 2020 May;24(5):309-317. doi: 10.1089/gtmb.2019.0255. Epub 2020 Apr 21. Genet Test Mol Biomarkers. 2020. PMID: 32315557 Free PMC article.

9

Comparative analysis of affected and unaffected areas of systemic sclerosis skin biopsies by high-throughput proteomic approaches.

Chairta P, Nicolaou P, Sokratous K, Galant C, Houssiau F, Oulas A, Spyrou GM, Alarcon-Riquelme ME, Lauwerys BR, Christodoulou K. Chairta P, et al. Among authors: nicolaou p. Arthritis Res Ther. 2020 May 7;22(1):107. doi: 10.1186/s13075-020-02196-x. Arthritis Res Ther. 2020. PMID: 32381114 Free PMC article.

10

A novel SLC30A10 missense variant associated with parkinsonism and dystonia without hypermanganesemia.

Lambrianides S, Nicolaou P, Michaelidou M, Kakouris P, Votsi C, Petrou PP, Drousiotou A, Minaidou A, Demetriou P, Voulgaris C, Christodoulou K, Tanteles GA, Pantzaris M. Lambrianides S, et al. Among authors: nicolaou p. J Neurol Sci. 2020 Nov 15;418:117101. doi: 10.1016/j.jns.2020.117101. Epub 2020 Aug 18. J Neurol Sci. 2020. PMID: 32866815 No abstract available.

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