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

Year Number of Results
1999 1
2009 1
2010 1
2012 1
2013 1
2014 3
2015 2
2017 2
2018 2
2020 2
2021 4
2022 8
2023 13
2024 3

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40 results

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Page 1
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Vetro A, Nielsen HN, Holm R, Hevner RF, Parrini E, Powis Z, Møller RS, Bellan C, Simonati A, Lesca G, Helbig KL, Palmer EE, Mei D, Ballardini E, Van Haeringen A, Syrbe S, Leuzzi V, Cioni G, Curry CJ, Costain G, Santucci M, Chong K, Mancini GMS, Clayton-Smith J, Bigoni S, Scheffer IE, Dobyns WB, Vilsen B, Guerrini R; ATP1A2/A3-collaborators. Vetro A, et al. Among authors: ballardini e. Brain. 2021 Jun 22;144(5):1435-1450. doi: 10.1093/brain/awab052. Brain. 2021. PMID: 33880529
PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.
Johannesen KM, Gardella E, Gjerulfsen CE, Bayat A, Rouhl RPW, Reijnders M, Whalen S, Keren B, Buratti J, Courtin T, Wierenga KJ, Isidor B, Piton A, Faivre L, Garde A, Moutton S, Tran-Mau-Them F, Denommé-Pichon AS, Coubes C, Larson A, Esser MJ, Appendino JP, Al-Hertani W, Gamboni B, Mampel A, Mayorga L, Orsini A, Bonuccelli A, Suppiej A, Van-Gils J, Vogt J, Damioli S, Giordano L, Moortgat S, Wirrell E, Hicks S, Kini U, Noble N, Stewart H, Asakar S, Cohen JS, Naidu SR, Collier A, Brilstra EH, Li MH, Brew C, Bigoni S, Ognibene D, Ballardini E, Ruivenkamp C, Faggioli R, Afenjar A, Rodriguez D, Bick D, Segal D, Coman D, Gunning B, Devinsky O, Demmer LA, Grebe T, Pruna D, Cursio I, Greenhalgh L, Graziano C, Singh RR, Cantalupo G, Willems M, Yoganathan S, Góes F, Leventer RJ, Colavito D, Olivotto S, Scelsa B, Andrade AV, Ratke K, Tokarz F, Khan AS, Ormieres C, Benko W, Keough K, Keros S, Hussain S, Franques A, Varsalone F, Grønborg S, Mignot C, Heron D, Nava C, Isapof A, Borlot F, Whitney R, Ronan A, Foulds N, Somorai M, Brandsema J, Helbig KL, Helbig I, Ortiz-González XR, Dubbs H, Vitobello A, Anderson M, Spadafore D, Hunt D, Møller RS, Rubboli G; PURA study group. Johannesen KM, et al. Among authors: ballardini e. Neurol Genet. 2021 Nov 15;7(6):e613. doi: 10.1212/NXG.0000000000000613. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34790866 Free PMC article.
Molecular genetic testing in athletes: Why and when a position statement from the Italian Society of Sports Cardiology.
Castelletti S, Zorzi A, Ballardini E, Basso C, Biffi A, Brancati F, Cavarretta E, Crotti L, Contursi M, D'Aleo A, D'Ascenzi F, Delise P, Dello Russo A, Gazale G, Mos L, Novelli V, Palamà Z, Palermi S, Palmieri V, Patrizi G, Pelliccia A, Pilichou K, Romano S, Sarto P, Schwartz PJ, Tiberi M, Zeppilli P, Corrado D, Sciarra L. Castelletti S, et al. Among authors: ballardini e. Int J Cardiol. 2022 Oct 1;364:169-177. doi: 10.1016/j.ijcard.2022.05.071. Epub 2022 Jun 1. Int J Cardiol. 2022. PMID: 35662561 Review.
Factors affecting yawning frequencies in preterm neonates.
Menin D, Ballardini E, Panebianco R, Garani G, Borgna-Pignatti C, Oster H, Dondi M. Menin D, et al. Among authors: ballardini e. PLoS One. 2022 May 6;17(5):e0268083. doi: 10.1371/journal.pone.0268083. eCollection 2022. PLoS One. 2022. PMID: 35522682 Free PMC article.
Gastrostomy and congenital anomalies: a European population-based study.
Garne E, Tan J, Loane M, Baldacci S, Ballardini E, Brigden J, Cavero-Carbonell C, García-Villodre L, Gissler M, Given J, Heino A, Jordan S, Limb E, Neville AJ, Rissmann A, Santoro M, Scanlon L, Urhoj SK, Wellesley DG, Morris J. Garne E, et al. Among authors: ballardini e. BMJ Paediatr Open. 2022 Jun;6(1):e001526. doi: 10.1136/bmjpo-2022-001526. BMJ Paediatr Open. 2022. PMID: 36053618 Free PMC article.
Different pre-term formulas for different pre-term infants.
Fanaro S, Ballardini E, Vigi V. Fanaro S, et al. Among authors: ballardini e. Early Hum Dev. 2010 Jul;86 Suppl 1:27-31. doi: 10.1016/j.earlhumdev.2010.01.005. Epub 2010 Feb 12. Early Hum Dev. 2010. PMID: 20153128 Review.
Accuracy of congenital anomaly coding in live birth children recorded in European health care databases, a EUROlinkCAT study.
Bakker MK, Loane M, Garne E, Ballardini E, Cavero-Carbonell C, García L, Gissler M, Given J, Heino A, Jamry-Dziurla A, Jordan S, Urhoj SK, Latos-Bieleńska A, Limb E, Lutke R, Neville AJ, Pierini A, Santoro M, Scanlon I, Tan J, Wellesley D, de Walle HEK, Morris JK. Bakker MK, et al. Among authors: ballardini e. Eur J Epidemiol. 2023 Mar;38(3):325-334. doi: 10.1007/s10654-023-00971-z. Epub 2023 Feb 18. Eur J Epidemiol. 2023. PMID: 36807730 Free PMC article.
Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study.
Divin N, Given JE, Tan J, Astolfi G, Ballardini E, Barrachina-Bonet L, Cavero-Carbonell C, Coi A, Garne E, Gissler M, Heino A, Jordan S, Pierini A, Scanlon I, Urhøj SK, Morris JK, Loane M. Divin N, et al. Among authors: ballardini e. BMJ Open. 2023 Oct 13;13(10):e068885. doi: 10.1136/bmjopen-2022-068885. BMJ Open. 2023. PMID: 37832979 Free PMC article.
Survival of children with rare structural congenital anomalies: a multi-registry cohort study.
Coi A, Santoro M, Pierini A, Rankin J, Glinianaia SV, Tan J, Reid AK, Garne E, Loane M, Given J, Ballardini E, Cavero-Carbonell C, de Walle HEK, Gatt M, García-Villodre L, Gissler M, Jordan S, Kiuru-Kuhlefelt S, Kjaer Urhoj S, Klungsøyr K, Lelong N, Lutke LR, Neville AJ, Rahshenas M, Scanlon I, Wellesley D, Morris JK. Coi A, et al. Among authors: ballardini e. Orphanet J Rare Dis. 2022 Mar 29;17(1):142. doi: 10.1186/s13023-022-02292-y. Orphanet J Rare Dis. 2022. PMID: 35351164 Free PMC article.
Epidemiology of aplasia cutis congenita: A population-based study in Europe.
Coi A, Barisic I, Garne E, Pierini A, Addor MC, Aizpurua Atxega A, Ballardini E, Braz P, Broughan JM, Cavero-Carbonell C, de Walle HEK, Draper ES, Gatt M, Häusler M, Kinsner-Ovaskainen A, Kurinczuk JJ, Lelong N, Luyt K, Mezzasalma L, Mullaney C, Nelen V, Odak L, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiśniewska K, Yevtushok L, Santoro M. Coi A, et al. Among authors: ballardini e. J Eur Acad Dermatol Venereol. 2023 Mar;37(3):581-589. doi: 10.1111/jdv.18690. Epub 2022 Nov 11. J Eur Acad Dermatol Venereol. 2023. PMID: 36300660 Free article.
40 results