GIACOMO GARONE

PhD Graduate

PhD program:: XXXVII


supervisor: Professor Pasquale Parisi

Thesis title: Tremor and Myoclonus: clinical, neurophysiological and neuroimaging phenotypes in children and adolescents

Tremor, defined as an involuntary rhythmic oscillatory movement, and myoclonus, characterized by brief, jerk-like movements, are distinct hyperkinetic movement disorders. Despite differences in their pathophysiology and clinical management, tremor and myoclonus are often confused due to their potentially similar presentations. Tremor and myoclonus are considered uncommon in children and adolescents, and few studies have investigated their causes and clinical features in the pediatric population. Therefore, the spectrum of clinical features and underlying causes of tremor and myoclonus in young patients remains only partially understood. Additionally, classification systems for tremor and myoclonus are largely based on adult-onset conditions, and their clinical applicability in children and adolescents has not yet been tested. The aim of this thesis is to dissect the phenotype of tremor and myoclonus in children and adolescents. By assessing a large cohort of patients with childhood-onset tremor and myoclonus, including the collection of clinical, neurophysiological and neuroimaging data, this project aims to address currently unanswered questions about these disorders in children. First, through a deep analysis of a large pediatric cohort, we tested whether the latest classification of tremor syndromes is applicable to childhood-onset tremor, analyzing specific peculiarities and diagnostic uncertainties. Second, we investigated the clinical phenotype of essential tremor in children, examining its neurophysiological features. Third, we explored whether co-occurring subtle neurological abnormalities in patients with essential tremor ("essential tremor plus") are associated with identifiable anatomical differences in brain volumetry. Fourth, we assessed the role of combined EEG-polymyography in the diagnosis of tremor and myoclonus, evaluating its utility in refining clinical diagnoses. Finally, we investigated the neurophysiological features of myoclonus in a cohort of affected children, focusing on the accuracy of polymyographic recordings in differentiating myoclonus subtypes.

Research products

11573/1717315 - 2024 - BCL11B-Related Dystonia: Further Evidence of an Emerging Cause of Childhood-Onset Generalized Dystonia
Garone, G.; Capuano, A.; Amodio, D.; Nicita, F.; Travaglini, L.; Graziola, F.; De Benedictis, A.; Frascarelli, F.; Parisi, P.; Pizzi, S.; Tartaglia, M.; Marras, C. E.; Niceta, M. - 01a Articolo in rivista
paper: MOVEMENT DISORDERS CLINICAL PRACTICE (Hoboken, NJ : John Wiley & Sons, 2014-) pp. 897-901 - issn: 2330-1619 - wos: WOS:001231782600001 (0) - scopus: 2-s2.0-85194700739 (1)

11573/1717316 - 2024 - Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology.
Garone, G.; Innocenti, A.; Grasso, M.; Mandarino, A.; Capuano, A.; Della Bella, G.; Frascarelli, F.; Diodato, D.; Onesimo, R.; Zampino, G.; Novelli, A.; Digilio, M. C.; Bartuli, A.; Dentici, M. L.; Parisi, P.; Galosi, S.; Tonduti, D.; Bertini, E.; Sinibaldi, L.; Specchio, N. - 01a Articolo in rivista
paper: PARKINSONISM & RELATED DISORDERS ([S.l.] : Elsevier Science) pp. 1-5 - issn: 1873-5126 - wos: WOS:001281943300001 (1) - scopus: 2-s2.0-85199495963 (1)

11573/1710311 - 2024 - Pediatric torticollis: clinical report and predictors of urgency of 1409 cases
Raucci, Umberto; Roversi, Marco; Ferretti, Alessandro; Faccia, Valerio; Garone, Giacomo; Panetta, Fabio; Mariani, Carlo; Rizzotto, Eloisa; Torelli, Antonio; Colafati, Giovanna Stefania; Aulisa, Angelo Gabriele; Parisi, Pasquale; Villani, Alberto - 01a Articolo in rivista
paper: THE ITALIAN JOURNAL OF PEDIATRICS (London : BioMed Central Ospedaletto : Pacini Editore) pp. - - issn: 1824-7288 - wos: WOS:001207714900002 (0) - scopus: 2-s2.0-85191332595 (1)

11573/1724441 - 2024 - Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
Sartorelli, J.; Travaglini, L.; Macchiaiolo, M.; Garone, G.; Gonfiantini, M. V.; Vecchio, D.; Sinibaldi, L.; Frascarelli, F.; Ceccatelli, V.; Petrillo, S.; Piemonte, F.; Piccolo, G.; Novelli, A.; Longo, D.; Pro, S.; D'amico, A.; Bertini, E. S.; Nicita, F. - 01a Articolo in rivista
paper: GENES (Basel : Molecular Diversity Preservation International) pp. - - issn: 2073-4425 - wos: WOS:001222274000001 (0) - scopus: 2-s2.0-85191520005 (1)

11573/1697336 - 2023 - Acute pupillary disorders in children: a 10-year retrospective study of 101 patients
Garone, Giacomo; Roversi, Marco; Pisani, Mara; La Penna, Francesco; Musolino, Antonio; Cristaldi, Sebastian; Musolino, Anna Maria; Roberto, Amanda; Petrocelli, Gianni; Reale, Antonino; Midulla, Fabio; Villani, Alberto; Raucci, Umberto - 01a Articolo in rivista
paper: CHILDREN (Basel: MDPI AG, 2014-) pp. - - issn: 2227-9067 - wos: WOS:001120723500001 (0) - scopus: 2-s2.0-85178149857 (1)

11573/1691726 - 2023 - Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies
Van Der Veen, Sterre; Tse, Gabrielle T W; Ferretti, Alessandro; Garone, Giacomo; Post, Bart; Specchio, Nicola; Fung, Victor S C; Trivisano, Marina; Scheffer, Ingrid E - 01a Articolo in rivista
paper: NEUROLOGY (Wolters Kluwer Hagerstown MD: Lippincott Williams & Wilkins Cleveland Ohio: Advanstar Communications) pp. 1884-1892 - issn: 0028-3878 - wos: WOS:001096235900016 (7) - scopus: 2-s2.0-85176508439 (7)

11573/1656386 - 2022 - “Spazio Huntington”: Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats
Graziola, F.; Maffi, S.; Grasso, M.; Garone, G.; Migliore, S.; Scaricamazza, E.; Ceccarelli, C.; Casella, M.; Busi, L.; D'alessio, B.; De Luca, A.; Colafati, G. S.; Sabatini, U.; Capuano, A.; Squitieri, F. - 01a Articolo in rivista
paper: JOURNAL OF PERSONALIZED MEDICINE (Basel: MDPI AG, 2011-) pp. 120- - issn: 2075-4426 - wos: WOS:000746970100001 (1) - scopus: 2-s2.0-85123173737 (2)

11573/1656388 - 2022 - Highlighting the Dystonic Phenotype Related to GNAO1
Wirth, Thomas; Garone, Giacomo; Kurian, Manju A; Piton, Amélie; Millan, Francisca; Telegrafi, Aida; Drouot, Nathalie; Rudolf, Gabrielle; Chelly, Jamel; Marks, Warren; Burglen, Lydie; Demailly, Diane; Coubes, Phillipe; Castro-Jimenez, Mayte; Joriot, Sylvie; Ghoumid, Jamal; Belin, Jérémie; Faucheux, Jean-Marc; Blumkin, Lubov; Hull, Mariam; Parnes, Mered; Ravelli, Claudia; Poulen, Gaëtan; Calmels, Nadège; Nemeth, Andrea H; Smith, Martin; Barnicoat, Angela; Ewenczyk, Claire; Méneret, Aurélie; Roze, Emmanuel; Keren, Boris; Mignot, Cyril; Beroud, Christophe; Acosta, Fernando; Nowak, Catherine; Wilson, William G; Steel, Dora; Capuano, Alessandro; Vidailhet, Marie; Lin, Jean-Pierre; Tranchant, Christine; Cif, Laura; Doummar, Diane; Anheim, Mathieu - 01a Articolo in rivista
paper: MOVEMENT DISORDERS (New York, N.Y. : John Wiley & Sons) pp. 1547-1554 - issn: 1531-8257 - wos: WOS:000812966100001 (1) - scopus: 2-s2.0-85132116614 (26)

11573/1656383 - 2021 - Acute movement disorders in childhood
Garone, G.; Graziola, F.; Grasso, M.; Capuano, A. - 01a Articolo in rivista
paper: JOURNAL OF CLINICAL MEDICINE (MDPI Publishing, Basel, Switzerland) pp. 2671- - issn: 2077-0383 - wos: WOS:000666521600001 (0) - scopus: 2-s2.0-85114067761 (3)

11573/1537309 - 2021 - Acute strabismus in neurological emergencies of childhood: a retrospective, single-centre study
Garone, Giacomo; Ferro, Valentina; Barbato, Marta; Vanacore, Nicola; Papini, Laura; Pro, Stefano; Boni, Alessandra; Scialanga, Barbara; Nacca, Raffaella; Evangelisti, Melania; Di Nardo, Giovanni; Parisi, Pasquale; Raucci, Umberto - 01a Articolo in rivista
paper: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (Harcourt Publishers Limited:Foots Cray High Street, Sidcup Kent DA14 5HP United Kingdom:011 44 20 83085700, EMAIL: journals@harcourt.com, INTERNET: http://www.harcourt-international.com, Fax: 011 44 20 83085876) pp. 80-85 - issn: 1090-3798 - wos: WOS:000655667500015 (2) - scopus: 2-s2.0-85104064621 (4)

11573/1656381 - 2021 - Cognitive assessment in GNAO1 neurodevelopmental disorder using an eye tracking system
Graziola, F.; Garone, G.; Grasso, M.; Capuano, A. - 01a Articolo in rivista
paper: JOURNAL OF CLINICAL MEDICINE (MDPI Publishing, Basel, Switzerland) pp. 3541- - issn: 2077-0383 - wos: WOS:000689261900001 (2) - scopus: 2-s2.0-85112217357 (8)

11573/1656380 - 2021 - Working memory, attention and planning abilities in NKX2.1-related chorea
Graziola, F.; Garone, G.; Grasso, M.; Schirinzi, T.; Capuano, A. - 01a Articolo in rivista
paper: PARKINSONISM & RELATED DISORDERS (Elsevier Science:Molenwarf 1, 1014 AG Amsterdam The Netherlands:011 31 20 4853597, EMAIL: p.j.bishop@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 31 20 4853249) pp. 24-27 - issn: 1353-8020 - wos: WOS:000671580100006 (0) - scopus: 2-s2.0-85108178739 (4)

11573/1580405 - 2021 - Cognitive deficits in children with brain tumours: A project to create a software for cognitive training
Mastronuzzi, Angela; Secco, Domitilla Elena; Laus, Beatrice; Carai, Andrea; Tozzi, Alberto; Premuselli, Roberto; Delli Priscoli, Francesco; Pietrabissa, Antonio; Giuseppi, Alessandro; Menegatti, Danilo; Rizzotto, Eloisa; Garone, Giacomo; Sciancalepore, Francesco; Lacorte, Eleonora; Tariciotti, Leonardo; Remoli, Giulia; Vanacore, Nicola; Raucci, Umberto - 04d Abstract in atti di convegno
paper: JOURNAL OF THE NEUROLOGICAL SCIENCES (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 161-161 - issn: 0022-510X - wos: WOS:000713637301270 (0) - scopus: (0)
conference: World Congress of Neurology (WCN 2021) (Rome, Italy)
book: Abstracts from the World Congress of Neurology (WCN 2021) - ()

11573/1656385 - 2020 - Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations
Barresi, S.; Dentici, M. L.; 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. - 01a Articolo in rivista
paper: PEDIATRIC NEUROLOGY (Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: (212)633-3680) pp. 40-45 - issn: 0887-8994 - wos: WOS:000517670500007 (11) - scopus: 2-s2.0-85076242925 (21)

11573/1656376 - 2020 - Alternating hemiplegia of childhood: Understanding the genotype–phenotype relationship of ATP1A3 variations
Capuano, A.; Garone, G.; Tiralongo, G.; Graziola, F. - 01a Articolo in rivista
paper: THE APPLICATION OF CLINICAL GENETICS ([Auckland, N.Z.] : Dove Medical Press, c2008-) pp. 71-81 - issn: 1178-704X - wos: WOS:000525747300001 (12) - scopus: 2-s2.0-85083856254 (24)

11573/1656379 - 2020 - Clinical and genetic overview of paroxysmal movement disorders and episodic ataxias
Garone, G.; Capuano, A.; Travaglini, L.; Graziola, F.; Stregapede, F.; Zanni, G.; Vigevano, F.; Bertini, E.; Nicita, F. - 01a Articolo in rivista
paper: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel (Matthaeustrasse 11) : Molecular Diversity Preservation International MDPI) pp. 3603- - issn: 1661-6596 - wos: WOS:000539312100199 (18) - scopus: 2-s2.0-85085265781 (44)

11573/1656387 - 2020 - 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, C. E.; Capuano, A. - 01a Articolo in rivista
paper: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (Cambridge University Press / New York:40 West 20th Street:New York, NY 10011:(800)872-7423, (212)924-3900, EMAIL: journals_subscriptions@cup.org, INTERNET: http://www.journals.cambridge.org, Fax: (212)691-3239) pp. 742-749 - issn: 0012-1622 - wos: WOS:000502462900001 (7) - scopus: 2-s2.0-85076756085 (13)

11573/1472362 - 2020 - Characteristics of acute nystagmus in the pediatric emergency department
Garone, G.; Suppiej, A.; Vanacore, N.; La Penna, F.; Parisi, P.; Calistri, L.; Palmieri, A.; Verrotti, A.; Poletto, E.; Rossetti, A.; Cordelli, D. M.; Velardita, M.; D'alonzo, R.; De Liso, P.; Gioe, D.; Marin, M.; Zagaroli, L.; Grosso, S.; Bonfatti, R.; Mencaroni, E.; Masi, S.; Bellelli, E.; Da Dalt, L.; Raucci, U. - 01a Articolo in rivista
paper: PEDIATRICS (American Academy of Pediatrics:141 Northwest Point Boulevard:Elk Grove Village, IL 60007:(800)433-9016, (847)434-4000, EMAIL: journals@aap.org, INTERNET: http://www.aap.org, Fax: (847)434-8000) pp. - - issn: 0031-4005 - wos: WOS:000562983100048 (8) - scopus: 2-s2.0-85089112069 (9)

11573/1656382 - 2020 - Impact of Italian lockdown on Tourette's syndrome patients at the time of the COVID-19 pandemic
Graziola, F.; Garone, G.; Di Criscio, L.; Grasso, M.; Curatolo, P.; Vigevano, F.; Capuano, A. - 01a Articolo in rivista
paper: PSYCHIATRY AND CLINICAL NEUROSCIENCES (-MALDEN:WILEY-BLACKWELL PUBLISHING, INC. -Carlton, Vic. : Blackwell Science, 1995-) pp. 610-612 - issn: 1323-1316 - wos: WOS:000564865000001 (7) - scopus: 2-s2.0-85090088218 (15)

11573/1656378 - 2019 - Vertical Gaze Palsy in Kernicterus
Garone, G.; Graziola, F.; Vigevano, F.; Capuano, A. - 01i Case report
paper: NEUROPEDIATRICS (Hippokrates Verlag GmbH:Postfach 300504, D-70445 Stuttgart Germany:011 49 711 89310, Fax: 011 49 711 8931706) pp. 262-263 - issn: 0174-304X - wos: WOS:000477664200009 (0) - scopus: 2-s2.0-85069189007 (0)

11573/1276660 - 2019 - Acute ataxia in paediatric emergency departments: a multicentre Italian study
Garone, Giacomo; Reale, Antonino; Vanacore, Nicola; Parisi, Pasquale; Bondone, Claudia; Suppiej, Agnese; Brisca, Giacomo; Calistri, Lucia; Cordelli, Duccio Maria; Savasta, Salvatore; Grosso, Salvatore; Midulla, Fabio; Falsaperla, Raffaele; Verrotti, Alberto; Bozzola, Elena; Vassia, Cristina; Da Dalt, Liviana; Maggiore, Rosario; Masi, Stefano; Maltoni, Lucia; Foiadelli, Thomas; Rossetti, Annalisa; Greco, Carla Maria; Marino, Silvia; Di Paolantonio, Claudia; Papetti, Laura; Urbino, Antonio Francesco; Rossi, Rossella; Raucci, Umberto - 01a Articolo in rivista
paper: ARCHIVES OF DISEASE IN CHILDHOOD (- London: BMJ Publishing Group - London: British Medical Association, 1926-) pp. - - issn: 0003-9888 - wos: WOS:000477897000014 (13) - scopus: 2-s2.0-85064006991 (33)

11573/1656374 - 2019 - 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. - 01a Articolo in rivista
paper: FRONTIERS IN GENETICS (Lausanne : Frontiers Research Foundation, 2010-) pp. - - issn: 1664-8021 - wos: WOS:000496133200001 (15) - scopus: 2-s2.0-85074775652 (22)

11573/1656377 - 2019 - 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. - 01i Case report
paper: PARKINSONISM & RELATED DISORDERS (Elsevier Science:Molenwarf 1, 1014 AG Amsterdam The Netherlands:011 31 20 4853597, EMAIL: p.j.bishop@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 31 20 4853249) pp. 4-6 - issn: 1353-8020 - wos: WOS:000468719900002 (14) - scopus: 2-s2.0-85064595562 (21)

11573/1227265 - 2019 - Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review
Schirinzi, Tommaso; Garone, Giacomo; Travaglini, Lorena; Vasco, Gessica; Galosi, Serena; Rios, Loreto; Castiglioni, Claudia; Barassi, Claudia; Battaglia, Domenica; Luigia Gambardella, Maria; Cantonetti, Laura; Graziola, Federica; Efisio Marras, Carlo; Castelli, Enrico; Bertini, Enrico; Capuano, Alessandro; Leuzzi, Vincenzo - 01g Articolo di rassegna (Review)
paper: PARKINSONISM & RELATED DISORDERS (Elsevier Science:Molenwarf 1, 1014 AG Amsterdam The Netherlands:011 31 20 4853597, EMAIL: p.j.bishop@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 31 20 4853249) pp. 19-25 - issn: 1353-8020 - wos: WOS:000468719900005 (56) - scopus: 2-s2.0-85059734550 (65)

11573/1199648 - 2018 - A cohort study on acute ocular motility disorders in pediatric emergency department
Raucci, Umberto; Parisi, Pasquale; Vanacore, Nicola; Ferro, Valentina; Garone, Giacomo; Sancetta, Federica; Petroni, Sergio; Pro, Stefano; Rossi, Rossella; Reale, Antonino; Pirozzi, Nicola - 01a Articolo in rivista
paper: THE ITALIAN JOURNAL OF PEDIATRICS (London: BioMed Central Ltd. 2008- -Pacini Editore) pp. 62-71 - issn: 1720-8424 - wos: WOS:000433930300002 (3) - scopus: 2-s2.0-85047728893 (3)

11573/1199625 - 2018 - Acute hyperkinetic movement disorders in Italian paediatric emergency departments
Raucci, Umberto; Parisi, Pasquale; Vanacore, Nicola; Garone, Giacomo; Bondone, Claudia; Palmieri, Antonella; Calistri, Lucia; Suppiej, Agnese; Falsaperla, Raffaele; Capuano, Alessandro; Ferro, Valentina; Urbino, Antonio Francesco; Tallone, Ramona; Montemaggi, Alessandra; Sartori, Stefano; Pavone, Piero; Mancardi, Margherita; Melani, Federico; Ilvento, Lucrezia; Pelizza, Maria Federica; Reale, Antonino - 01a Articolo in rivista
paper: ARCHIVES OF DISEASE IN CHILDHOOD (- London: BMJ Publishing Group - London: British Medical Association, 1926-) pp. 790-794 - issn: 0003-9888 - wos: WOS:000440170800019 (12) - scopus: 2-s2.0-85049222173 (11)

11573/856715 - 2016 - Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region
Nicita, Francesco; Garone, Giacomo; Spalice, Alberto; Savasta, Salvatore; Striano, Pasquale; Pantaleoni, Chiara; Spartà, Maria Valentina; Kluger, Gerhard; Capovilla, Giuseppe; Pruna, Dario; Freri, Elena; D'arrigo, Stefano; Verrotti, Alberto - 01a Articolo in rivista
paper: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 148-55-155 - issn: 1552-4825 - wos: WOS:000367933600019 (25) - scopus: 2-s2.0-84955472591 (22)

11573/931351 - 2016 - The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome
Papetti, Laura; Schettini, Livia; Garone, Giacomo; Gennaro, Elena; Malacarne, Michela; Properzi, Enrico; Spalice, Alberto - 01f Lettera, Nota
paper: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 3041-3042 - issn: 1552-4825 - wos: WOS:000388195300039 (4) - scopus: 2-s2.0-84969932836 (4)

11573/856713 - 2015 - Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy
Nicita, Francesco; Garone, Giacomo; Papetti, Laura; Consoli, Federica; Magliozzi, Monia; De Luca, Alessandro; Spalice, Alberto - 01a Articolo in rivista
paper: JOURNAL OF NEUROGENETICS (Taylor & Francis Limited:Rankine Road, Basingstoke RG24 8PR United Kingdom:011 44 1256 813035, EMAIL: madeline.sims@tandf.co.uk, info@tandf.co.uk, INTERNET: http://www.tandf.co.uk, Fax: 011 44 1256 330245) pp. 178-82-182 - issn: 0167-7063 - wos: WOS:000369293800004 (1) - scopus: 2-s2.0-84956766615 (1)

11573/856716 - 2015 - Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1
Nicita, Francesco; Ulgiati, Fiorenza; Bernardini, Laura; Garone, Giacomo; Papetti, Laura; Novelli, Antonio; Spalice, Alberto - 01a Articolo in rivista
paper: ANNALS OF HUMAN GENETICS (Cambridge : Cambridge University Press 1954- Oxford : Blackwell Science,) pp. 209-217 - issn: 1469-1809 - wos: WOS:000353646400006 (11) - scopus: 2-s2.0-84946727775 (11)

11573/788376 - 2015 - Severe early onset ethylmalonic encephalopathy with west syndrome
Papetti, Laura; Garone, Giacomo; Schettini, Laura; Giordano, Carla; Nicita, Francesco; Papoff, Paola; Zeviani, M; Leuzzi, Vincenzo; Spalice, Alberto - 01i Case report
paper: METABOLIC BRAIN DISEASE (Plenum Press:Book Customer Service, 233 Spring Street:New York, NY 10013:(212)620-8471, (212)620-8000, EMAIL: info@plenum.com, INTERNET: http://www.plenum.com, Fax: (212)807-1047) pp. 1537-1545 - issn: 0885-7490 - wos: WOS:000365086600025 (12) - scopus: 2-s2.0-84947030750 (13)

© Università degli Studi di Roma "La Sapienza" - Piazzale Aldo Moro 5, 00185 Roma