Nicolaou P - Search Results

1

LRSAM1 Depletion Affects Neuroblastoma SH-SY5Y Cell Growth and Morphology: The LRSAM1 c.2047-1G>A Loss-of-Function Variant Fails to Rescue The Phenotype.

Minaidou A, Nicolaou P, Christodoulou K. Minaidou A, et al. Among authors: nicolaou p. Cell J. 2018 Oct;20(3):340-347. doi: 10.22074/cellj.2018.5352. Epub 2018 May 15. Cell J. 2018. PMID: 29845787 Free PMC article.

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

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.

Kleopa KA, Zamba-Papanicolaou E, Alevra X, Nicolaou P, Georgiou DM, Hadjisavvas A, Kyriakides T, Christodoulou K. Kleopa KA, et al. Among authors: nicolaou p. Neurology. 2006 Feb 14;66(3):396-402. doi: 10.1212/01.wnl.0000196479.93722.59. Neurology. 2006. PMID: 16476939

4

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

5

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.

6

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

7

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.

8

Genetic findings of Cypriot spinal muscular atrophy patients.

Theodorou L, Nicolaou P, Koutsou P, Georghiou A, Anastasiadou V, Tanteles G, Kyriakides T, Zamba-Papanicolaou E, Christodoulou K. Theodorou L, et al. Among authors: nicolaou p. Neurol Sci. 2015 Oct;36(10):1829-34. doi: 10.1007/s10072-015-2263-5. Epub 2015 May 28. Neurol Sci. 2015. PMID: 26017350

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

64 results

Search Page

Filters