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Year Number of Results
2015 4
2016 2
2018 5
2019 7
2020 4
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17 results
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Page 1
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review.
Schirinzi T, Garone G, Travaglini L, Vasco G, Galosi S, Rios L, Castiglioni C, Barassi C, Battaglia D, Gambardella ML, Cantonetti L, Graziola F, Marras CE, Castelli E, Bertini E, Capuano A, Leuzzi V. Schirinzi T, et al. Among authors: Garone G. Parkinsonism Relat Disord. 2019 Apr;61:19-25. doi: 10.1016/j.parkreldis.2018.11.019. Epub 2018 Nov 16. Parkinsonism Relat Disord. 2019. PMID: 30642806 Review.
Acute ataxia in paediatric emergency departments: a multicentre Italian study.
Garone G, Reale A, Vanacore N, Parisi P, Bondone C, Suppiej A, Brisca G, Calistri L, Cordelli DM, Savasta S, Grosso S, Midulla F, Falsaperla R, Verrotti A, Bozzola E, Vassia C, Da Dalt L, Maggiore R, Masi S, Maltoni L, Foiadelli T, Rossetti A, Greco C, Marino S, Di Paolantonio C, Papetti L, Urbino AF, Rossi R, Raucci U. Garone G, et al. Arch Dis Child. 2019 Aug;104(8):768-774. doi: 10.1136/archdischild-2018-315487. Epub 2019 Apr 4. Arch Dis Child. 2019. PMID: 30948362 Clinical Trial.
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.
Nicita F, Garone G, Spalice A, Savasta S, Striano P, Pantaleoni C, Spartà MV, Kluger G, Capovilla G, Pruna D, Freri E, D'Arrigo S, Verrotti A. Nicita F, et al. Among authors: Garone G. Am J Med Genet A. 2016 Jan;170A(1):148-55. doi: 10.1002/ajmg.a.37410. Epub 2015 Oct 5. Am J Med Genet A. 2016. PMID: 26437767
Acute hyperkinetic movement disorders in Italian paediatric emergency departments.
Raucci U, Parisi P, Vanacore N, Garone G, Bondone C, Palmieri A, Calistri L, Suppiej A, Falsaperla R, Capuano A, Ferro V, Urbino AF, Tallone R, Montemaggi A, Sartori S, Pavone P, Mancardi M, Melani F, Ilvento L, Pelizza MF, Reale A. Raucci U, et al. Among authors: Garone G. Arch Dis Child. 2018 Aug;103(8):790-794. doi: 10.1136/archdischild-2017-314464. Epub 2018 Mar 8. Arch Dis Child. 2018. PMID: 29519947 Clinical Trial.
Vertical Gaze Palsy in Kernicterus.
Garone G, Graziola F, Vigevano F, Capuano A. Garone G, et al. Neuropediatrics. 2019 Aug;50(4):262-263. doi: 10.1055/s-0039-1685527. Epub 2019 May 7. Neuropediatrics. 2019. PMID: 31064023 No abstract available.
The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome.
Papetti L, Schettini L, Garone G, Gennaro E, Malacarne M, Properzi E, Spalice A. Papetti L, et al. Among authors: Garone G. Am J Med Genet A. 2016 Nov;170(11):3041-3042. doi: 10.1002/ajmg.a.37753. Epub 2016 May 17. Am J Med Genet A. 2016. PMID: 27184008 No abstract available.
A cohort study on acute ocular motility disorders in pediatric emergency department.
Raucci U, Parisi P, Vanacore N, Ferro V, Garone G, Sancetta F, Petroni S, Pro S, Rossi R, Reale A, Pirozzi N. Raucci U, et al. Among authors: Garone G. Ital J Pediatr. 2018 May 29;44(1):62. doi: 10.1186/s13052-018-0502-0. Ital J Pediatr. 2018. PMID: 29843812 Free PMC article.
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1.
Nicita F, Ulgiati F, Bernardini L, Garone G, Papetti L, Novelli A, Spalice A. Nicita F, et al. Among authors: Garone G. Ann Hum Genet. 2015 May;79(3):209-17. doi: 10.1111/ahg.12106. Epub 2015 Mar 16. Ann Hum Genet. 2015. PMID: 25779878 Free article.
Severe early onset ethylmalonic encephalopathy with West syndrome.
Papetti L, Garone G, Schettini L, Giordano C, Nicita F, Papoff P, Zeviani M, Leuzzi V, Spalice A. Papetti L, et al. Among authors: Garone G. Metab Brain Dis. 2015 Dec;30(6):1537-45. doi: 10.1007/s11011-015-9707-8. Epub 2015 Jul 21. Metab Brain Dis. 2015. PMID: 26194623
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