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

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

15 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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: grafakou o. 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.
Valproate effect on ketosis in children under ketogenic diet.
Spilioti M, Pavlou E, Gogou M, Katsanika I, Papadopoulou-Alataki E, Grafakou O, Gkampeta A, Dinopoulos A, Evangeliou A. Spilioti M, et al. Among authors: grafakou o. Eur J Paediatr Neurol. 2016 Jul;20(4):555-9. doi: 10.1016/j.ejpn.2016.04.003. Epub 2016 Apr 13. Eur J Paediatr Neurol. 2016. PMID: 27117552 Clinical Trial.
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: grafakou o. 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.
Can chest X-ray predict pneumonia severity?
Grafakou O, Moustaki M, Tsolia M, Kavazarakis E, Mathioudakis J, Fretzayas A, Nicolaidou P, Karpathios T. Grafakou O, et al. Pediatr Pulmonol. 2004 Dec;38(6):465-9. doi: 10.1002/ppul.20112. Pediatr Pulmonol. 2004. PMID: 15481079
A case series of Cypriot patients with CblC defect: Clinical, biochemical and molecular characteristics.
Georgiou T, Grafakou O, Malekkou A, Athanasiou E, Ioannou I, Choleva V, Dionysiou M, Mavrikiou G, Demetriadou A, Anastasiadou V, Drousiotou A, Petrou PP. Georgiou T, et al. Among authors: grafakou o. Mol Genet Metab Rep. 2024 Nov 9;41:101158. doi: 10.1016/j.ymgmr.2024.101158. eCollection 2024 Dec. Mol Genet Metab Rep. 2024. PMID: 39584041 Free PMC article.
Health and well-being of maturing adults with classic galactosemia.
Garrett OS, Druss JJ, Vos EN, Fu YD, Lucia S, Greenstein PE, Bauer A, Sykut-Cegielska J, Stepien KM, Arbuckle C, Grafakou O, Meyer U, Vanhoutvin N, Pané A, Bosch AM, Rubio-Gozalbo E, Berry GT, Fridovich-Keil JL. Garrett OS, et al. Among authors: grafakou o. J Inherit Metab Dis. 2025 Jan;48(1):e12786. doi: 10.1002/jimd.12786. Epub 2024 Aug 14. J Inherit Metab Dis. 2025. PMID: 39143820 Free PMC article.
15 results