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Items: 1 to 50 of 60

1.

A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.

Diquigiovanni C, Bergamini C, Diaz R, Liparulo I, Bianco F, Masin L, Baldassarro VA, Rizzardi N, Tranchina A, Buscherini F, Wischmeijer A, Pippucci T, Scarano E, Cordelli DM, Fato R, Seri M, Paracchini S, Bonora E.

FASEB J. 2019 Oct;33(10):11284-11302. doi: 10.1096/fj.201802722R. Epub 2019 Aug 7.

PMID:
31314595
2.

Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study.

Di Pisa V, Provini F, Ubertiello S, Bonetti S, Ricci E, Ivanovski I, Caraffi SG, Giordano L, Accorsi P, Savasta S, Raviglione F, Boni A, Grioni D, Graziano C, Garavelli L, Cordelli DM.

Sleep Med. 2019 Sep;61:44-51. doi: 10.1016/j.sleep.2019.04.011. Epub 2019 Apr 26.

PMID:
31285160
3.

Myoclonic epilepsy with photosensitivity in infants with Pallister-Killian Syndrome.

Ricci E, Bonfatti R, Rocca A, Sperti G, Cagnazzo V, Vignoli A, Cocchi G, Cordelli DM.

Eur J Paediatr Neurol. 2019 Jul;23(4):653-656. doi: 10.1016/j.ejpn.2019.05.012. Epub 2019 May 25.

PMID:
31178275
4.

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
5.

Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts.

Milev MP, Graziano C, Karall D, Kuper WFE, Al-Deri N, Cordelli DM, Haack TB, Danhauser K, Iuso A, Palombo F, Pippucci T, Prokisch H, Saint-Dic D, Seri M, Stanga D, Cenacchi G, van Gassen KLI, Zschocke J, Fauth C, Mayr JA, Sacher M, van Hasselt PM.

J Med Genet. 2018 Nov;55(11):753-764. doi: 10.1136/jmedgenet-2018-105441. Epub 2018 Aug 17.

PMID:
30120216
6.

Pediatric epilepsies misdiagnosed as gastrointestinal disorders.

Carbonari G, Tonti G, Di Pisa V, Franzoni E, Cordelli DM.

Epilepsy Behav. 2018 Jun;83:137-139. doi: 10.1016/j.yebeh.2018.03.034. Epub 2018 Apr 26.

PMID:
29705623
7.

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.

Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L.

Genet Med. 2018 Sep;20(9):965-975. doi: 10.1038/gim.2017.221. Epub 2018 Jan 4.

PMID:
29300384
8.

Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212].

Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G.

J Neurol Sci. 2018 Feb 15;385:238. doi: 10.1016/j.jns.2017.12.002. Epub 2017 Dec 15. No abstract available.

PMID:
29254810
9.

A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.

Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G.

J Neurol Sci. 2017 Oct 15;381:209-212. doi: 10.1016/j.jns.2017.08.3260. Epub 2017 Sep 1. Erratum in: J Neurol Sci. 2017 Dec 15;:.

PMID:
28991683
10.

Acute diplopia in the pediatric Emergency Department. A cohort multicenter Italian study.

Raucci U, Parisi P, Vanacore N, La Penna F, Ferro V, Calistri L, Bondone C, Midulla F, Suppiej A, Falsaperla R, Cordelli DM, Palmieri A, Verrotti A, Becciani S, Aguzzi S, Mastrangelo M, Pelizza F, Greco F, Carbonari G, Tallone R, Bottone G, Trenta I, Masi S, Villa MP, Reale A.

Eur J Paediatr Neurol. 2017 Sep;21(5):722-729. doi: 10.1016/j.ejpn.2017.05.010. Epub 2017 Jun 3.

PMID:
28625338
11.

Central Nervous System Complications in Children Receiving Chemotherapy or Hematopoietic Stem Cell Transplantation.

Cordelli DM, Masetti R, Zama D, Toni F, Castelli I, Ricci E, Franzoni E, Pession A.

Front Pediatr. 2017 May 15;5:105. doi: 10.3389/fped.2017.00105. eCollection 2017. Review.

12.

Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.

Jenkinson EM, Rodero MP, Kasher PR, Uggenti C, Oojageer A, Goosey LC, Rose Y, Kershaw CJ, Urquhart JE, Williams SG, Bhaskar SS, O'Sullivan J, Baerlocher GM, Haubitz M, Aubert G, Barañano KW, Barnicoat AJ, Battini R, Berger A, Blair EM, Brunstrom-Hernandez JE, Buckard JA, Cassiman DM, Caumes R, Cordelli DM, De Waele LM, Fay AJ, Ferreira P, Fletcher NA, Fryer AE, Goel H, Hemingway CA, Henneke M, Hughes I, Jefferson RJ, Kumar R, Lagae L, Landrieu PG, Lourenço CM, Malpas TJ, Mehta SG, Metz I, Naidu S, Õunap K, Panzer A, Prabhakar P, Quaghebeur G, Schiffmann R, Sherr EH, Sinnathuray KR, Soh C, Stewart HS, Stone J, Van Esch H, Van Mol CE, Vanderver A, Wakeling EL, Whitney A, Pavitt GD, Griffiths-Jones S, Rice GI, Revy P, van der Knaap MS, Livingston JH, O'Keefe RT, Crow YJ.

Nat Genet. 2017 Jan 31;49(2):317. doi: 10.1038/ng0217-317b. No abstract available.

PMID:
28138155
13.

Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.

Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR.

Genet Med. 2017 Jun;19(6):691-700. doi: 10.1038/gim.2016.176. Epub 2016 Nov 10.

14.

Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.

Jenkinson EM, Rodero MP, Kasher PR, Uggenti C, Oojageer A, Goosey LC, Rose Y, Kershaw CJ, Urquhart JE, Williams SG, Bhaskar SS, O'Sullivan J, Baerlocher GM, Haubitz M, Aubert G, Barañano KW, Barnicoat AJ, Battini R, Berger A, Blair EM, Brunstrom-Hernandez JE, Buckard JA, Cassiman DM, Caumes R, Cordelli DM, De Waele LM, Fay AJ, Ferreira P, Fletcher NA, Fryer AE, Goel H, Hemingway CA, Henneke M, Hughes I, Jefferson RJ, Kumar R, Lagae L, Landrieu PG, Lourenço CM, Malpas TJ, Mehta SG, Metz I, Naidu S, Õunap K, Panzer A, Prabhakar P, Quaghebeur G, Schiffmann R, Sherr EH, Sinnathuray KR, Soh C, Stewart HS, Stone J, Van Esch H, Van Mol CE, Vanderver A, Wakeling EL, Whitney A, Pavitt GD, Griffiths-Jones S, Rice GI, Revy P, van der Knaap MS, Livingston JH, O'Keefe RT, Crow YJ.

Nat Genet. 2016 Oct;48(10):1185-92. doi: 10.1038/ng.3661. Epub 2016 Aug 29. Erratum in: Nat Genet. 2017 Jan 31;49(2):317.

15.

Juvenile dermatomyositis: A report of three cases.

Papa V, Romanin B, Bergamaschi R, Cordelli DM, Costa R, De Giorgi LB, Cenacchi G.

Ultrastruct Pathol. 2016;40(2):83-5. doi: 10.3109/01913123.2016.1141823. Epub 2016 Feb 17.

PMID:
26886841
16.

Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.

Carrozzo R, Verrigni D, Rasmussen M, de Coo R, Amartino H, Bianchi M, Buhas D, Mesli S, Naess K, Born AP, Woldseth B, Prontera P, Batbayli M, Ravn K, Joensen F, Cordelli DM, Santorelli FM, Tulinius M, Darin N, Duno M, Jouvencel P, Burlina A, Stangoni G, Bertini E, Redonnet-Vernhet I, Wibrand F, Dionisi-Vici C, Uusimaa J, Vieira P, Osorio AN, McFarland R, Taylor RW, Holme E, Ostergaard E.

J Inherit Metab Dis. 2016 Mar;39(2):243-52. doi: 10.1007/s10545-015-9894-9. Epub 2015 Oct 16.

PMID:
26475597
17.

New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer.

Severi G, Bernardini L, Briuglia S, Bigoni S, Buldrini B, Magini P, Dentici ML, Cordelli DM, Arrigo T, Franzoni E, Fini S, Italyankina E, Loddo I, Novelli A, Graziano C.

Am J Med Genet A. 2016 Jan;170A(1):162-9. doi: 10.1002/ajmg.a.37346. Epub 2015 Sep 3.

PMID:
26333654
18.

Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.

Magini P, Poscente M, Ferrari S, Vargiolu M, Bacchelli E, Graziano C, Wischmeijer A, Turchetti D, Malaspina E, Marchiani V, Cordelli DM, Franzoni E, Romeo G, Seri M.

Mol Cytogenet. 2015 Aug 1;8:58. doi: 10.1186/s13039-015-0164-1. eCollection 2015.

19.

PRES in Children Undergoing Hematopoietic Stem Cell or Solid Organ Transplantation.

Masetti R, Cordelli DM, Zama D, Vendemini F, Biagi C, Franzoni E, Pession A.

Pediatrics. 2015 May;135(5):890-901. doi: 10.1542/peds.2014-2325. Review.

20.

Risk factor analysis of posterior reversible encephalopathy syndrome after allogeneic hematopoietic SCT in children.

Zama D, Masetti R, Cordelli DM, Vendemini F, Giordano L, Milito G, Franzoni E, Porta F, Prete A, Rondelli R, Pession A.

Bone Marrow Transplant. 2014 Dec;49(12):1538-40. doi: 10.1038/bmt.2014.182. Epub 2014 Aug 18. No abstract available.

PMID:
25133894
21.

Cerebral ischemic involvement in Vogt-Koyanagi-Harada disease.

Vergaro R, Cordelli DM, Miniaci A, Tassinari D, Spinardi L, Pession A, Franzoni E.

Pediatr Neurol. 2014 Jul;51(1):119-22. doi: 10.1016/j.pediatrneurol.2014.03.004. Epub 2014 Mar 15.

PMID:
24830768
22.

Life-threatening complications of posterior reversible encephalopathy syndrome in children.

Cordelli DM, Masetti R, Ricci E, Toni F, Zama D, Maffei M, Gentili A, Parmeggiani A, Pession A, Franzoni E.

Eur J Paediatr Neurol. 2014 Sep;18(5):632-40. doi: 10.1016/j.ejpn.2014.04.014. Epub 2014 Apr 25.

PMID:
24814477
23.

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.

Magini P, Pippucci T, Tsai IC, Coppola S, Stellacci E, Bartoletti-Stella A, Turchetti D, Graziano C, Cenacchi G, Neri I, Cordelli DM, Marchiani V, Bergamaschi R, Gasparre G, Neri G, Mazzanti L, Patrizi A, Franzoni E, Romeo G, Bordo D, Tartaglia M, Katsanis N, Seri M.

Hum Mol Genet. 2014 Jul 1;23(13):3607-17. doi: 10.1093/hmg/ddu070. Epub 2014 Feb 19.

PMID:
24556213
24.

Inflammatory disease of the central nervous system induced by anti-GD2 monoclonal antibody in a patient with high risk neuroblastoma.

Zama D, Morello W, Masetti R, Cordelli DM, Massaccesi E, Prete A, Pession A.

Pediatr Blood Cancer. 2014 Aug;61(8):1521-2. doi: 10.1002/pbc.24982. Epub 2014 Feb 17. No abstract available.

PMID:
24535934
25.

Leukoencephalopathy with calcifications and cysts: a purely neurological disorder distinct from coats plus.

Livingston JH, Mayer J, Jenkinson E, Kasher P, Stivaros S, Berger A, Cordelli DM, Ferreira P, Jefferson R, Kutschke G, Lundberg S, Ounap K, Prabhakar P, Soh C, Stewart H, Stone J, van der Knaap MS, van Esch H, van Mol C, Wakeling E, Whitney A, Rice GI, Crow YJ.

Neuropediatrics. 2014 Jun;45(3):175-82. doi: 10.1055/s-0033-1364180. Epub 2014 Jan 9.

PMID:
24407470
26.

Etiology, characteristics and outcome of seizures after pediatric hematopoietic stem cell transplantation.

Cordelli DM, Masetti R, Zama D, Gueraldi D, Rondelli R, Cottone C, Prete A, Pession A, Franzoni E.

Seizure. 2014 Feb;23(2):140-5. doi: 10.1016/j.seizure.2013.11.003. Epub 2013 Nov 13.

27.

Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.

Giordano L, Vignoli A, Cusmai R, Parisi P, Mastrangelo M, Coppola G, Cordelli DM, Accorsi P, Milito G, Darra F, Pruna D, Belcastro V, Verrotti A, Striano P.

Epilepsia. 2013 Oct;54 Suppl 7:66-9. doi: 10.1111/epi.12311.

28.

Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA?

Cordelli DM, Pellicciari A, Kiriazopulos D, Franzoni E, Garavelli L.

Epilepsia. 2013 Jul;54(7):1331-2. doi: 10.1111/epi.12204. No abstract available.

29.

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.

Cordelli DM, Garavelli L, Savasta S, Guerra A, Pellicciari A, Giordano L, Bonetti S, Cecconi I, Wischmeijer A, Seri M, Rosato S, Gelmini C, Della Giustina E, Ferrari AR, Zanotta N, Epifanio R, Grioni D, Malbora B, Mammi I, Mari F, Buoni S, Mostardini R, Grosso S, Pantaleoni C, Doz M, Poch-Olivé ML, Rivieri F, Sorge G, Simonte G, Licata F, Tarani L, Terazzi E, Mazzanti L, Cerruti Mainardi P, Boni A, Faravelli F, Grasso M, Bianchi P, Zollino M, Franzoni E.

Am J Med Genet A. 2013 Feb;161A(2):273-84. doi: 10.1002/ajmg.a.35717. Epub 2013 Jan 15.

PMID:
23322667
30.

Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype.

Quattrocchi CC, Zanni G, Napolitano A, Longo D, Cordelli DM, Barresi S, Randisi F, Valente EM, Verdolotti T, Genovese E, Specchio N, Vitiello G, Spiegel R, Bertini E, Bernardi B.

Neurogenetics. 2013 Feb;14(1):77-83. doi: 10.1007/s10048-012-0352-7. Epub 2012 Dec 30.

PMID:
23274687
31.

Psychotic episode during steroid therapy in hashimoto encephalopathy.

Pellicciari A, Cordelli DM, Leo I, Di Pietro E, Aldrovandi A, Franzoni E.

J Neuropsychiatry Clin Neurosci. 2012 Winter;24(1):E45-6. doi: 10.1176/appi.neuropsych.11030061. No abstract available.

PMID:
22450647
32.

Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.

Guerrini R, Mei D, Cordelli DM, Pucatti D, Franzoni E, Parrini E.

Eur J Hum Genet. 2012 Sep;20(9):995-8. doi: 10.1038/ejhg.2012.21. Epub 2012 Feb 15.

33.

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.

Anderson BH, Kasher PR, Mayer J, Szynkiewicz M, Jenkinson EM, Bhaskar SS, Urquhart JE, Daly SB, Dickerson JE, O'Sullivan J, Leibundgut EO, Muter J, Abdel-Salem GM, Babul-Hirji R, Baxter P, Berger A, Bonafé L, Brunstom-Hernandez JE, Buckard JA, Chitayat D, Chong WK, Cordelli DM, Ferreira P, Fluss J, Forrest EH, Franzoni E, Garone C, Hammans SR, Houge G, Hughes I, Jacquemont S, Jeannet PY, Jefferson RJ, Kumar R, Kutschke G, Lundberg S, Lourenço CM, Mehta R, Naidu S, Nischal KK, Nunes L, Ounap K, Philippart M, Prabhakar P, Risen SR, Schiffmann R, Soh C, Stephenson JB, Stewart H, Stone J, Tolmie JL, van der Knaap MS, Vieira JP, Vilain CN, Wakeling EL, Wermenbol V, Whitney A, Lovell SC, Meyer S, Livingston JH, Baerlocher GM, Black GC, Rice GI, Crow YJ.

Nat Genet. 2012 Jan 22;44(3):338-42. doi: 10.1038/ng.1084.

PMID:
22267198
34.

Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic study.

Cordelli DM, Aldrovandi A, Gentile V, Garone C, Conti S, Aceti A, Gennaro E, Zara F, Franzoni E.

Seizure. 2012 Mar;21(2):141-3. doi: 10.1016/j.seizure.2011.09.013. Epub 2011 Oct 19.

35.

Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation.

Cordelli DM, Masetti R, Bernardi B, Barcia G, Gentile V, Biagi C, Prete A, Pession A, Franzoni E.

Pediatr Blood Cancer. 2012 May;58(5):785-90. doi: 10.1002/pbc.23344. Epub 2011 Oct 11.

PMID:
21990274
36.

The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration.

Chiapparini L, Savoiardo M, D'Arrigo S, Reale C, Zorzi G, Zibordi F, Cordelli DM, Franzoni E, Garavaglia B, Nardocci N.

Neuropediatrics. 2011 Aug;42(4):159-62. doi: 10.1055/s-0031-1285925. Epub 2011 Aug 29.

PMID:
21877312
37.

FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype.

Garone C, Pippucci T, Cordelli DM, Zuntini R, Castegnaro G, Marconi C, Graziano C, Marchiani V, Verrotti A, Seri M, Franzoni E.

Dev Med Child Neurol. 2011 Oct;53(10):958-61. doi: 10.1111/j.1469-8749.2011.03993.x. Epub 2011 May 18.

38.

Diagnosis of congenital myasthenic syndrome with mutation of the RAPSN gene after general anaesthesia.

Gentili A, Ansaloni S, Morello W, Cecini MT, Cordelli DM, Baroncini S.

Eur J Anaesthesiol. 2011 Oct;28(10):748-9. doi: 10.1097/EJA.0b013e3283453f4b. No abstract available.

PMID:
21372719
39.

VNS in drug resistant epilepsy: preliminary report on a small group of patients.

Franzoni E, Gentile V, Colonnelli MC, Brunetto D, Cecconi I, Iero L, Moscano FC, Cordelli DM, Marchiani V.

Ital J Pediatr. 2010 Apr 14;36:30. doi: 10.1186/1824-7288-36-30.

40.

Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN).

Cordelli DM, Garone C, Marchiani V, Lodi R, Tonon C, Ferrari S, Seri M, Franzoni E.

Neuromuscul Disord. 2010 May;20(5):343-5. doi: 10.1016/j.nmd.2010.03.003. Epub 2010 Mar 28.

PMID:
20350809
41.

Bathing epilepsy: report of two Caucasian cases.

Franzoni E, Gentile V, Grosso S, Brunetto D, Cordelli DM, Balestri P.

Epileptic Disord. 2010 Mar;12(1):88-90. doi: 10.1684/epd.2010.0295. Epub 2010 Feb 26.

42.

Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy.

Franzoni E, Gentile V, Pellicciari A, Garone C, Iero L, Gualandi S, Cordelli DM, Cecconi I, Moscano FC, Marchiani V, Errani A.

J Neurol. 2009 Sep;256(9):1527-32. doi: 10.1007/s00415-009-5157-8. Epub 2009 Jul 14.

PMID:
19597919
43.

Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review.

Grosso S, Cordelli DM, Coppola G, Franzoni E, Verrotti A, Berardi R, Balestri P.

Eur J Neurol. 2008 Sep;15(9):940-6. doi: 10.1111/j.1468-1331.2008.02215.x. Epub 2008 Jul 10.

PMID:
18637038
44.

Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy.

Grosso S, Cordelli DM, Franzoni E, Coppola G, Capovilla G, Zamponi N, Verrotti A, Morgese G, Balestri P.

Seizure. 2007 Jun;16(4):345-50. Epub 2007 Mar 26.

45.

Sensorial saturation for neonatal analgesia.

Bellieni CV, Cordelli DM, Marchi S, Ceccarelli S, Perrone S, Maffei M, Buonocore G.

Clin J Pain. 2007 Mar-Apr;23(3):219-21.

PMID:
17314580
46.

Inter-observer reliability of two pain scales for newborns.

Bellieni CV, Cordelli DM, Caliani C, Palazzi C, Franci N, Perrone S, Bagnoli F, Buonocore G.

Early Hum Dev. 2007 Aug;83(8):549-52. Epub 2006 Dec 11.

PMID:
17161923
47.

Analgesic effect of watching TV during venipuncture.

Bellieni CV, Cordelli DM, Raffaelli M, Ricci B, Morgese G, Buonocore G.

Arch Dis Child. 2006 Dec;91(12):1015-7. Epub 2006 Aug 18.

48.

Ante partum bed rest and unexplained infantile crying.

Bellieni CV, Odent M, Cordelli FM, Cordelli DM, Bagnoli F, Perrone S, Buonocore G.

Minerva Pediatr. 2005 Aug;57(4):163-6.

PMID:
16172594
49.

Is an excessive number of prenatal echographies a risk for fetal growth?

Bellieni CV, Buonocore G, Bagnoli F, Cordelli DM, Gasparre O, Calonaci F, Filardi G, Merola A, Petraglia F.

Early Hum Dev. 2005 Aug;81(8):689-93.

PMID:
16005167
50.

Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy.

Grosso S, Franzoni E, Coppola G, Iannetti P, Verrotti A, Cordelli DM, Marchiani V, Pascotto A, Spalice A, Acampora B, Morgese G, Balestri P.

Seizure. 2005 Jun;14(4):248-53.

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