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Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years.
J Neuromuscul Dis. 2020;7(3):247-256. doi: 10.3233/JND-190466.
J Neuromuscul Dis. 2020.
PMID: 32417790
Free PMC article.
Single amino acid loss in the dystrophin protein associated with a mild clinical phenotype.
Pons R, Kekou K, Gkika A, Papadimas G, Vogiatzakis N, Svingou M, Papadopooulos C, Nikas I, Dinopoulos A, Youroukos S, Kanavakis E.
Pons R, et al. Among authors: dinopoulos a.
Muscle Nerve. 2017 Jan;55(1):46-50. doi: 10.1002/mus.25190. Epub 2016 Oct 28.
Muscle Nerve. 2017.
PMID: 27178005
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A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.
Polymeris AA, Tessa A, Anagnostopoulou K, Rubegni A, Galatolo D, Dinopoulos A, Gika AD, Youroukos S, Skouteli E, Santorelli FM, Pons R.
Polymeris AA, et al. Among authors: dinopoulos a.
J Neurol. 2016 Aug;263(8):1604-11. doi: 10.1007/s00415-016-8179-z. Epub 2016 Jun 3.
J Neurol. 2016.
PMID: 27260292
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Sleep architecture and epileptic characteristics of drug naïve patients in childhood absence epilepsy spectrum. A prospective study.
Dinopoulos A, Tsirouda MA, Bonakis A, Pons R, Pavlopoulou ID, Tsoumakas K.
Dinopoulos A, et al.
Seizure. 2018 Jul;59:99-107. doi: 10.1016/j.seizure.2018.04.021. Epub 2018 Apr 30.
Seizure. 2018.
PMID: 29787924
Free article.
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Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes.
Zaganas I, Vorgia P, Spilioti M, Mathioudakis L, Raissaki M, Ilia S, Giorgi M, Skoula I, Chinitrakis G, Michaelidou K, Paraskevoulakos E, Grafakou O, Kariniotaki C, Psyllou T, Zafeiris S, Tzardi M, Briassoulis G, Dinopoulos A, Mitsias P, Evangeliou A.
Zaganas I, et al. Among authors: dinopoulos a.
Epilepsy Behav Rep. 2021 Aug 27;16:100477. doi: 10.1016/j.ebr.2021.100477. eCollection 2021.
Epilepsy Behav Rep. 2021.
PMID: 34568804
Free PMC article.
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Osteoporosis-pseudoglioma syndrome: clinical, genetic, and treatment-response study of 10 new cases in Greece.
Papadopoulos I, Bountouvi E, Attilakos A, Gole E, Dinopoulos A, Peppa M, Nikolaidou P, Papadopoulou A.
Papadopoulos I, et al. Among authors: dinopoulos a.
Eur J Pediatr. 2019 Mar;178(3):323-329. doi: 10.1007/s00431-018-3299-3. Epub 2018 Nov 29.
Eur J Pediatr. 2019.
PMID: 30499050
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Structural mapping of GABRB3 variants reveals genotype-phenotype correlations.
Johannesen KM, Iqbal S, Guazzi M, Mohammadi NA, Pérez-Palma E, Schaefer E, De Saint Martin A, Abiwarde MT, McTague A, Pons R, Piton A, Kurian MA, Ambegaonkar G, Firth H, Sanchis-Juan A, Deprez M, Jansen K, De Waele L, Briltra EH, Verbeek NE, van Kempen M, Fazeli W, Striano P, Zara F, Visser G, Braakman HMH, Haeusler M, Elbracht M, Vaher U, Smol T, Lemke JR, Platzer K, Kennedy J, Klein KM, Au PYB, Smyth K, Kaplan J, Thomas M, Dewenter MK, Dinopoulos A, Campbell AJ, Lal D, Lederer D, Liao VWY, Ahring PK, Møller RS, Gardella E.
Johannesen KM, et al. Among authors: dinopoulos a.
Genet Med. 2022 Mar;24(3):681-693. doi: 10.1016/j.gim.2021.11.004. Epub 2021 Dec 7.
Genet Med. 2022.
PMID: 34906499
Free article.
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Coinheritance of Noonan syndrome and Becker muscular dystrophy.
Dinopoulos A, Papadopoulou A, Manta P, Kekou K, Kanelopoulos T, Fretzayas A, Kitsiou S.
Dinopoulos A, et al.
Neuromuscul Disord. 2010 Jan;20(1):61-3. doi: 10.1016/j.nmd.2009.08.008. Epub 2009 Oct 28.
Neuromuscul Disord. 2010.
PMID: 19875288
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Antiphospholipid and Antinuclear Antibodies in Children with Idiopathic Epilepsy: A 2-Year Prospective Study.
Attilakos A, Fotis L, Dinopoulos A, Alexopoulos H, Theofilopoulou AV, Tzioufas AG, Mastroyianni S, Karalexi M, Garoufi A.
Attilakos A, et al. Among authors: dinopoulos a.
J Clin Neurol. 2020 Jan;16(1):140-144. doi: 10.3988/jcn.2020.16.1.140.
J Clin Neurol. 2020.
PMID: 31942770
Free PMC article.
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Effect of levetiracetam monotherapy on lipid profiles and thyroid hormones in children with epilepsy: A prospective study.
Attilakos A, Dinopoulos A, Tsirouda M, Paschalidou M, Prasouli A, Stamati A, Parasxou N, Garoufi A.
Attilakos A, et al. Among authors: dinopoulos a.
Epilepsy Res. 2019 Sep;155:106162. doi: 10.1016/j.eplepsyres.2019.106162. Epub 2019 Jul 4.
Epilepsy Res. 2019.
PMID: 31301589
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