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Truncated prelamin A expression in HGPS-like patients: a transcriptional study.
Eur J Hum Genet. 2015 Aug;23(8):1051-61. doi: 10.1038/ejhg.2014.239. Epub 2015 Feb 4.
Eur J Hum Genet. 2015.
PMID: 25649378
Free PMC article.
Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete.
Evangeliou A, Lionis C, Michailidou H, Spilioti M, Kanitsakis A, Nikitakis P, Drakonakis N, Giannakopoulou C, Sbyrakis S, Sewell AC, Boehles HJ, Smeitink J, Wevers RA.
Evangeliou A, et al. Among authors: spilioti m.
J Inherit Metab Dis. 2001 Dec;24(8):877-80. doi: 10.1023/a:1013904627537.
J Inherit Metab Dis. 2001.
PMID: 11916324
No abstract available.
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The significance of opthalmologic evaluation in the early diagnosis of inborn errors of metabolism: the Cretan experience.
Tsagaraki DP, Evangeliou AE, Tsilimbaris M, Spilioti MG, Mihailidou EP, Lionis C, Pallikaris I.
Tsagaraki DP, et al. Among authors: spilioti mg.
BMC Ophthalmol. 2002 Apr 11;2:2. doi: 10.1186/1471-2415-2-2.
BMC Ophthalmol. 2002.
PMID: 11950394
Free PMC article.
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Decreased cortical excitability due to a large venous angioma.
Spilioti M, Ameridou I, Ilias A, Evangeliou A, Amoiridis G.
Spilioti M, et al.
Pediatr Neurol. 2006 Dec;35(6):433-5. doi: 10.1016/j.pediatrneurol.2006.06.019.
Pediatr Neurol. 2006.
PMID: 17138015
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Strabismus and nystagmus in a 4-year-old boy.
Raissaki M, Spilioti M, Kalaidopoulou P, Iliaki O, Mavrokosta M, Nikolaidis N, Evangeliou A.
Raissaki M, et al. Among authors: spilioti m.
Pediatr Ann. 2008 Sep;37(9):590-3. doi: 10.3928/00904481-20080901-03.
Pediatr Ann. 2008.
PMID: 18795568
No abstract available.
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Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.
Lefeber DJ, Schönberger J, Morava E, Guillard M, Huyben KM, Verrijp K, Grafakou O, Evangeliou A, Preijers FW, Manta P, Yildiz J, Grünewald S, Spilioti M, van den Elzen C, Klein D, Hess D, Ashida H, Hofsteenge J, Maeda Y, van den Heuvel L, Lammens M, Lehle L, Wevers RA.
Lefeber DJ, et al. Among authors: spilioti m.
Am J Hum Genet. 2009 Jul;85(1):76-86. doi: 10.1016/j.ajhg.2009.06.006. Epub 2009 Jul 2.
Am J Hum Genet. 2009.
PMID: 19576565
Free PMC article.
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Ketogenic diet in a patient with Angelman syndrome.
Evangeliou A, Doulioglou V, Haidopoulou K, Aptouramani M, Spilioti M, Varlamis G.
Evangeliou A, et al. Among authors: spilioti m.
Pediatr Int. 2010 Oct;52(5):831-4. doi: 10.1111/j.1442-200X.2010.03118.x.
Pediatr Int. 2010.
PMID: 20880305
No abstract available.
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Evaluation of Oral Glucose Tolerance Test in Children With Epilepsy.
Varlamis S, Vavatsi N, Pavlou E, Kotsis V, Spilioti M, Kavga M, Varlamis G, Sotiriadou F, Agakidou E, Voutoufianakis S, Evangeliou AE.
Varlamis S, et al. Among authors: spilioti m.
J Child Neurol. 2013 Nov;28(11):1437-1442. doi: 10.1177/0883073812460919. Epub 2012 Oct 15.
J Child Neurol. 2013.
PMID: 23071070
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Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD).
Spilioti M, Evangeliou AE, Tramma D, Theodoridou Z, Metaxas S, Michailidi E, Bonti E, Frysira H, Haidopoulou A, Asprangathou D, Tsalkidis AJ, Kardaras P, Wevers RA, Jakobs C, Gibson KM.
Spilioti M, et al.
Front Hum Neurosci. 2013 Dec 24;7:858. doi: 10.3389/fnhum.2013.00858. eCollection 2013.
Front Hum Neurosci. 2013.
PMID: 24399946
Free PMC article.
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Succinic Semialdehyde Dehydrogenase Deficiency Presenting as Autism Spectrum Disorder.
Gogou M, Spilioti M, Tramma D, Papadopoulou-Alataki E, Evangeliou A.
Gogou M, et al. Among authors: spilioti m.
Indian J Pediatr. 2016 Sep;83(9):1036-7. doi: 10.1007/s12098-015-2003-0. Epub 2016 Jan 25.
Indian J Pediatr. 2016.
PMID: 26806207
No abstract available.
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