Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 2
1986 4
1987 2
1988 3
1989 4
1991 2
1992 3
1993 1
1994 1
1995 2
1996 1
1997 3
1998 1
2000 1
2001 1
2002 3
2004 3
2005 6
2006 6
2007 3
2008 3
2009 4
2010 3
2011 3
2013 6
2014 4
2015 3
2016 4
2017 4
2018 9
2019 7
2020 9
2021 9
2022 8
2023 7
2024 7
2025 7

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

132 results

Results by year

Filters applied: . Clear all
Page 1
N-Acetyl-leucine in progressive CACNA1A ataxia: A case series.
Martakis K, Giorgi M, Spanou M, Neubauer BA, Dinopoulos A, Hahn A. Martakis K, et al. Among authors: dinopoulos a. Eur J Paediatr Neurol. 2025 Jan;54:64-67. doi: 10.1016/j.ejpn.2024.12.006. Epub 2025 Jan 2. Eur J Paediatr Neurol. 2025. PMID: 39765122 Free article.
Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders.
Armirola-Ricaurte C, Zonnekein N, Koutsis G, Amor-Barris S, Pelayo-Negro AL, Atkinson D, Efthymiou S, Turchetti V, Dinopoulos A, Garcia A, Karakaya M, Moris G, Polat AI, Yiş U, Espinos C, Van de Vondel L, De Vriendt E, Karadima G, Wirth B, Hanna M, Houlden H, Berciano J, Jordanova A. Armirola-Ricaurte C, et al. Among authors: dinopoulos a. Genet Med. 2024 Jun;26(6):101117. doi: 10.1016/j.gim.2024.101117. Epub 2024 Mar 6. Genet Med. 2024. PMID: 38459834 Free PMC article.
Conversion disorder in a preschool age girl.
Bouras G, Michopoulos I, Theofanopoulou N, Giannopoulou I, Christodoulou C, Dinopoulos A. Bouras G, et al. Among authors: dinopoulos a. J Health Psychol. 2016 Nov;21(11):2668-2672. doi: 10.1177/1359105315583368. Epub 2016 Jul 10. J Health Psychol. 2016. PMID: 25972349
Partial loss of FITM2 function causes hereditary spastic paraplegia.
Salazar-Villacorta A, Bond LM, Kim L, Anagnostopoulou K, Scardamaglia A, Filippakopoulou E, Ververi A, Efthymiou S, Dinopoulos A, Murphy D, Karadima G, Koutsis G, Kaliakatsos M, Houlden H, Walther TC, Farese RV. Salazar-Villacorta A, et al. Among authors: dinopoulos a. medRxiv [Preprint]. 2025 Jan 25:2025.01.23.24319660. doi: 10.1101/2025.01.23.24319660. medRxiv. 2025. PMID: 39974099 Free PMC article. Preprint.
Motor phenotyping in a Greek cohort of patients with neonatal and infantile onset developmental and epileptic encephalopathy.
Kollia E, Kokkinou E, Outsika C, Koltsida G, Zouvelou V, Vontzalidis A, Dalivigka Z, Veltra D, Sofocleous C, Marinakis NM, Tilemis FN, Yapijakis C, Anagnostopoulou KK, Loukas YL, Spanou M, Dinopoulos A, Nikaina E, Skiathitou AV, Siahanidou T, Georgiadou E, Moudaki A, Lykopoulou E, Pons R. Kollia E, et al. Among authors: dinopoulos a. Eur J Paediatr Neurol. 2025 Mar;55:1-8. doi: 10.1016/j.ejpn.2025.03.001. Epub 2025 Mar 3. Eur J Paediatr Neurol. 2025. PMID: 40068485
Erythromelalgia in an Adolescent Female.
Mamatsi E, Giorgi M, Dinopoulos A, Papaevangelou V, Fotis L. Mamatsi E, et al. Among authors: dinopoulos a. Mediterr J Rheumatol. 2022 Jun 30;33(2):256-258. doi: 10.31138/mjr.33.2.256. eCollection 2022 Jun. Mediterr J Rheumatol. 2022. PMID: 36128208 Free PMC article.
The orthopaedic aspect of spastic cerebral palsy.
Skoutelis VC, Kanellopoulos AD, Kontogeorgakos VA, Dinopoulos A, Papagelopoulos PJ. Skoutelis VC, et al. Among authors: dinopoulos a. J Orthop. 2020 Nov 4;22:553-558. doi: 10.1016/j.jor.2020.11.002. eCollection 2020 Nov-Dec. J Orthop. 2020. PMID: 33214743 Free PMC article. Review.
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.
132 results