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Items: 19

1.

Prestatus and status dystonicus in children and adolescents.

Garone G, Graziola F, Nicita F, Frascarelli F, Randi F, Zazza M, Cantonetti L, Cossu S, Marras CE, Capuano A.

Dev Med Child Neurol. 2019 Dec 13. doi: 10.1111/dmcn.14425. [Epub ahead of print]

PMID:
31837011
2.

Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations.

Barresi S, Dentici ML, Manzoni F, Bellacchio E, Agolini E, Pizzi S, Ciolfi A, Tarnopolsky M, Brady L, Garone G, Novelli A, Mei D, Guerrini R, Capuano A, Pantaleoni C, Tartaglia M.

Pediatr Neurol. 2019 Oct 19. pii: S0887-8994(19)30881-1. doi: 10.1016/j.pediatrneurol.2019.09.005. [Epub ahead of print]

PMID:
31836334
3.

Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study.

Graziola F, Garone G, Stregapede F, Bosco L, Vigevano F, Curatolo P, Bertini E, Travaglini L, Capuano A.

Front Genet. 2019 Oct 29;10:1026. doi: 10.3389/fgene.2019.01026. eCollection 2019.

4.

Vertical Gaze Palsy in Kernicterus.

Garone G, Graziola F, Vigevano F, Capuano A.

Neuropediatrics. 2019 Aug;50(4):262-263. doi: 10.1055/s-0039-1685527. Epub 2019 May 7. No abstract available.

PMID:
31064023
5.

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.

Arch Dis Child. 2019 Aug;104(8):768-774. doi: 10.1136/archdischild-2018-315487. Epub 2019 Apr 4.

PMID:
30948362
6.

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.

Parkinsonism Relat Disord. 2019 Apr;61:19-25. doi: 10.1016/j.parkreldis.2018.11.019. Epub 2018 Nov 16. Review.

PMID:
30642806
7.

A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder.

Graziola F, Stregapede F, Travaglini L, Garone G, Verardo M, Bosco L, Pro S, Bertini E, Curatolo P, Vigevano F, Capuano A.

Parkinsonism Relat Disord. 2019 Apr;61:4-6. doi: 10.1016/j.parkreldis.2018.12.001. Epub 2018 Dec 7. No abstract available.

PMID:
30579817
8.

Could Rolandic spikes be a prognostic factor of the neurocognitive outcome of children with BECTS?

Tristano I, Nicita F, Garone G, Ursitti F, Nardone C, Rocchi V, Guido CA, Spalice A.

Epilepsy Behav. 2018 Sep;86:157-162. doi: 10.1016/j.yebeh.2018.03.022. Epub 2018 Jul 19.

PMID:
30031676
9.

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.

Ital J Pediatr. 2018 May 29;44(1):62. doi: 10.1186/s13052-018-0502-0.

10.

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.

Arch Dis Child. 2018 Aug;103(8):790-794. doi: 10.1136/archdischild-2017-314464. Epub 2018 Mar 8.

PMID:
29519947
11.

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.

Am J Med Genet A. 2016 Nov;170(11):3041-3042. doi: 10.1002/ajmg.a.37753. Epub 2016 May 17. No abstract available.

PMID:
27184008
12.

Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy.

Nicita F, Garone G, Papetti L, Consoli F, Magliozzi M, De Luca A, Spalice A.

J Neurogenet. 2015;29(4):178-82. doi: 10.3109/01677063.2015.1091452. Epub 2015 Nov 11.

PMID:
26559560
13.

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.

Am J Med Genet A. 2016 Jan;170A(1):148-55. doi: 10.1002/ajmg.a.37410. Epub 2015 Oct 5.

PMID:
26437767
14.

Rationale and design for the Vaginal Erbium Laser Academy Study (VELAS): an international multicenter observational study on genitourinary syndrome of menopause and stress urinary incontinence.

Gambacciani M, Torelli MG, Martella L, Bracco GL, Casagrande AG, Albertin E, Tabanelli S, Viglietta M, D'Ambrogio G, Garone G, Cervigni M.

Climacteric. 2015;18 Suppl 1:43-8. doi: 10.3109/13697137.2015.1071608.

PMID:
26366800
15.

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.

Metab Brain Dis. 2015 Dec;30(6):1537-45. doi: 10.1007/s11011-015-9707-8. Epub 2015 Jul 21.

PMID:
26194623
16.

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.

Ann Hum Genet. 2015 May;79(3):209-17. doi: 10.1111/ahg.12106. Epub 2015 Mar 16.

17.

[Evaluation of the use of the partogram in the Obstetrico-Gynecologic Division of the Seregno Hospital].

Re G, Garone G.

Ann Ostet Ginecol Med Perinat. 1983 Jul-Aug;104(4):270-81. Italian. No abstract available.

PMID:
6660742
18.

[Evolution of endometrial hyperplasia in the pre-menopausal period. 10-year analysis of 885 cases in 2 Milan hospitals].

Carnio P, Garone G, Gambacorta M, Re MP, Scaglione V, Remotti G.

Ann Ostet Ginecol Med Perinat. 1983 Mar-Apr;104(2):125-39. Review. Italian. No abstract available.

PMID:
6349497
19.

[Treatment of segmental cervical incompetence in pregnancy. Surgical indications, technic and results of 128 cervical cerclage operations].

Bonfadini Bossi E, Migliavacca AE, Fagnani D, Salini P, Rella R, Garone G, Buratti E, Gasparotto G.

Minerva Ginecol. 1981 Apr;33(4):385-8. Italian. No abstract available.

PMID:
7243082

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