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Items: 1 to 50 of 121

1.

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.

Trivisano M, Pietrafusa N, Terracciano A, Marini C, Mei D, Darra F, Accorsi P, Battaglia D, Caffi L, Canevini MP, Cappelletti S, Cesaroni E, de Palma L, Costa P, Cusmai R, Giordano L, Ferrari A, Freri E, Fusco L, Granata T, Martino T, Mastrangelo M, Bova SM, Parmeggiani L, Ragona F, Sicca F, Striano P, Specchio LM, Tondo I, Zambrelli E, Zamponi N, Zanus C, Boniver C, Vecchi M, Avolio C, Dalla Bernardina B, Bertini E, Guerrini R, Vigevano F, Specchio N.

Epilepsia. 2018 Dec;59(12):2260-2271. doi: 10.1111/epi.14600. Epub 2018 Nov 19.

PMID:
30451291
2.

Diaper changing-induced reflex seizures in CDKL5-related epilepsy.

Solazzi R, Fiorini E, Parrini E, Darra F, Dalla Bernardina B, Cantalupo G.

Epileptic Disord. 2018 Oct 1;20(5):428-433. doi: 10.1684/epd.2018.0999.

PMID:
30378547
3.

Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).

Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A.

Acta Neurol Scand. 2018 Jun;137(6):575-581. doi: 10.1111/ane.12902. Epub 2018 Jan 23.

PMID:
29363096
4.

EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency.

Pellegrin S, Cantalupo G, Opri R, Dalla Bernardina B, Darra F.

Eur J Paediatr Neurol. 2017 May;21(3):580-582. doi: 10.1016/j.ejpn.2017.01.002. Epub 2017 Jan 17.

PMID:
28129950
5.

Epilepsy in ring chromosome 20 syndrome.

Vignoli A, Bisulli F, Darra F, Mastrangelo M, Barba C, Giordano L, Turner K, Zambrelli E, Chiesa V, Bova S, Fiocchi I, Peron A, Naldi I, Milito G, Licchetta L, Tinuper P, Guerrini R, Dalla Bernardina B, Canevini MP.

Epilepsy Res. 2016 Dec;128:83-93. doi: 10.1016/j.eplepsyres.2016.10.004. Epub 2016 Oct 24.

PMID:
27816898
6.

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study.

Vecchi M, Barba C, De Carlo D, Stivala M, Guerrini R, Albamonte E, Ranalli D, Battaglia D, Lunardi G, Boniver C, Piccolo B, Pisani F, Cantalupo G, Nieddu G, Casellato S, Cappanera S, Cesaroni E, Zamponi N, Serino D, Fusco L, Iodice A, Palestra F, Giordano L, Freri E, De Giorgi I, Ragona F, Granata T, Fiocchi I, Bova SM, Mastrangelo M, Verrotti A, Matricardi S, Fontana E, Caputo D, Darra F, Dalla Bernardina B, Beccaria F, Capovilla G, Baglietto MP, Gagliardi A, Vignoli A, Canevini MP, Perissinotto E, Francione S.

Epilepsia. 2016 Nov;57(11):1808-1816. doi: 10.1111/epi.13574. Epub 2016 Oct 20.

7.

Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.

Opri R, Fabrizi GM, Cantalupo G, Ferrarini M, Simonati A, Dalla Bernardina B, Darra F.

Seizure. 2016 Nov;42:1-6. doi: 10.1016/j.seizure.2016.08.008. Epub 2016 Sep 5. Review.

8.

Pediatric epilepsy following neonatal seizures symptomatic of stroke.

Suppiej A, Mastrangelo M, Mastella L, Accorsi P, Grazian L, Casara G, Peruzzi C, Carpanelli ML, Janes A, Traverso A, Dalla Bernardina B.

Brain Dev. 2016 Jan;38(1):27-31. doi: 10.1016/j.braindev.2015.05.010. Epub 2015 Jun 6.

PMID:
26058328
9.

Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series.

Sartori S, Nosadini M, Cesaroni E, Falsaperla R, Capovilla G, Beccaria F, Mancardi MM, Santangelo G, Giunta L, Boniver C, Cantalupo G, Cappellari A, Costa P, Dalla Bernardina B, Dilena R, Natali Sora MG, Pelizza MF, Pruna D, Serino D, Vanadia F, Vigevano F, Zamponi N, Zanus C, Toldo I, Suppiej A.

Eur J Paediatr Neurol. 2015 Jul;19(4):453-63. doi: 10.1016/j.ejpn.2015.02.006. Epub 2015 Mar 3.

PMID:
25792293
10.

Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys.

Mei D, Darra F, Barba C, Marini C, Fontana E, Chiti L, Parrini E, Dalla Bernardina B, Guerrini R.

Epilepsia. 2014 Nov;55(11):1748-53. doi: 10.1111/epi.12803. Epub 2014 Sep 29.

11.

Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.

Verrotti A, Cusmai R, Darra F, Martelli P, Accorsi P, Bergamo S, Bevivino E, Coppola G, Freri E, Grosso S, Matricardi S, Parisi P, Sartori S, Spalice A, Specchio N, Carelli A, Zini D, Dalla Bernardina B, Giordano L.

Epilepsy Res. 2014 Nov;108(9):1597-603. doi: 10.1016/j.eplepsyres.2014.08.006. Epub 2014 Aug 30.

PMID:
25218893
12.

Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI study.

Vaudano AE, Ruggieri A, Vignoli A, Avanzini P, Benuzzi F, Gessaroli G, Nichelli PF, Darra F, Cantalupo G, Mastrangelo M, Dalla Bernardina B, Canevini MP, Meletti S.

Epilepsia. 2014 Mar;55(3):403-13. doi: 10.1111/epi.12539. Epub 2014 Jan 31.

13.

Clinical dissection of early onset absence epilepsy in children and prognostic implications.

Agostinelli S, Accorsi P, Beccaria F, Belcastro V, Canevini MP, Capovilla G, Cappanera S, Dalla Bernardina B, Darra F, Del Gaudio L, Elia M, Falsaperla R, Giordano L, Gobbi G, Minetti C, Nicita F, Parisi P, Pavone P, Pezzella M, Sesta M, Spalice A, Striano S, Tozzi E, Traverso M, Vari S, Vignoli A, Zamponi N, Zara F, Striano P, Verrotti A; SINP (Società Italiana Neurologia Pediatrica) Collaborative Working Group.

Epilepsia. 2013 Oct;54(10):1761-70. doi: 10.1111/epi.12341. Epub 2013 Aug 27.

14.

Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20.

Avanzini P, Vaudano AE, Vignoli A, Ruggieri A, Benuzzi F, Darra F, Mastrangelo M, Dalla Bernardina B, Nichelli PF, Canevini MP, Meletti S.

Clin Neurophysiol. 2014 Feb;125(2):239-49. doi: 10.1016/j.clinph.2013.07.009. Epub 2013 Aug 19.

PMID:
23968845
15.

Idiopathic generalized epilepsies.

Caraballo RH, Dalla Bernardina B.

Handb Clin Neurol. 2013;111:579-89. doi: 10.1016/B978-0-444-52891-9.00060-9. Review.

PMID:
23622205
16.

Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution.

Agostinelli S, Traverso M, Accorsi P, Beccaria F, Belcastro V, Capovilla G, Cappanera S, Coppola A, Dalla Bernardina B, Darra F, Ferretti M, Elia M, Galeone D, Giordano L, Gobbi G, Nicita F, Parisi P, Pezzella M, Spalice A, Striano S, Tozzi E, Vignoli A, Minetti C, Zara F, Striano P, Verrotti A.

Eur J Neurol. 2013 May;20(5):856-9. doi: 10.1111/j.1468-1331.2012.03871.x. Epub 2012 Sep 30.

17.

Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.

Marini C, Darra F, Specchio N, Mei D, Terracciano A, Parmeggiani L, Ferrari A, Sicca F, Mastrangelo M, Spaccini L, Canopoli ML, Cesaroni E, Zamponi N, Caffi L, Ricciardelli P, Grosso S, Pisano T, Canevini MP, Granata T, Accorsi P, Battaglia D, Cusmai R, Vigevano F, Dalla Bernardina B, Guerrini R.

Epilepsia. 2012 Dec;53(12):2111-9. doi: 10.1111/j.1528-1167.2012.03649.x. Epub 2012 Sep 4.

18.

Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases.

Liava A, Francione S, Tassi L, Lo Russo G, Cossu M, Mai R, Darra F, Fontana E, Dalla Bernardina B.

Epilepsy Behav. 2012 Sep;25(1):68-80. doi: 10.1016/j.yebeh.2012.05.008. Epub 2012 Aug 17.

PMID:
22902651
19.

PRRT2 mutations are the major cause of benign familial infantile seizures.

Schubert J, Paravidino R, Becker F, Berger A, Bebek N, Bianchi A, Brockmann K, Capovilla G, Dalla Bernardina B, Fukuyama Y, Hoffmann GF, Jurkat-Rott K, Anttonen AK, Kurlemann G, Lehesjoki AE, Lehmann-Horn F, Mastrangelo M, Mause U, Müller S, Neubauer B, Püst B, Rating D, Robbiano A, Ruf S, Schroeder C, Seidel A, Specchio N, Stephani U, Striano P, Teichler J, Turkdogan D, Vigevano F, Viri M, Bauer P, Zara F, Lerche H, Weber YG.

Hum Mutat. 2012 Oct;33(10):1439-43. doi: 10.1002/humu.22126. Epub 2012 Jun 11.

PMID:
22623405
20.

Oxidative stress-related biomarkers in autism: systematic review and meta-analyses.

Frustaci A, Neri M, Cesario A, Adams JB, Domenici E, Dalla Bernardina B, Bonassi S.

Free Radic Biol Med. 2012 May 15;52(10):2128-41. doi: 10.1016/j.freeradbiomed.2012.03.011. Epub 2012 Apr 18. Review.

PMID:
22542447
21.

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.

Bonaglia MC, Giorda R, Beri S, De Agostini C, Novara F, Fichera M, Grillo L, Galesi O, Vetro A, Ciccone R, Bonati MT, Giglio S, Guerrini R, Osimani S, Marelli S, Zucca C, Grasso R, Borgatti R, Mani E, Motta C, Molteni M, Romano C, Greco D, Reitano S, Baroncini A, Lapi E, Cecconi A, Arrigo G, Patricelli MG, Pantaleoni C, D'Arrigo S, Riva D, Sciacca F, Dalla Bernardina B, Zoccante L, Darra F, Termine C, Maserati E, Bigoni S, Priolo E, Bottani A, Gimelli S, Bena F, Brusco A, di Gregorio E, Bagnasco I, Giussani U, Nitsch L, Politi P, Martinez-Frias ML, Martínez-Fernández ML, Martínez Guardia N, Bremer A, Anderlid BM, Zuffardi O.

PLoS Genet. 2011 Jul;7(7):e1002173. doi: 10.1371/journal.pgen.1002173. Epub 2011 Jul 14.

22.

Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life.

Sartori S, Polli R, Bettella E, Rossato S, Andreoli W, Vecchi M, Giordano L, Accorsi P, Di Rosa G, Toldo I, Zamponi N, Darra F, Dalla Bernardina B, Perilongo G, Boniver C, Murgia A.

J Child Neurol. 2011 Jun;26(6):683-91. doi: 10.1177/0883073810387827. Epub 2011 Apr 11.

PMID:
21482751
23.

The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus.

Veggiotti P, Burlina A, Coppola G, Cusmai R, De Giorgis V, Guerrini R, Tagliabue A, Dalla Bernardina B.

Epilepsia. 2011 Apr;52 Suppl 2:83-9. doi: 10.1111/j.1528-1167.2011.03010.x. Review.

24.

Electroencephalographic characteristics of Dravet syndrome.

Bureau M, Dalla Bernardina B.

Epilepsia. 2011 Apr;52 Suppl 2:13-23. doi: 10.1111/j.1528-1167.2011.02996.x. Review.

25.

Severe myoclonic epilepsy in infancy (Dravet syndrome) 30 years later.

Dravet C, Bureau M, Dalla Bernardina B, Guerrini R.

Epilepsia. 2011 Apr;52 Suppl 2:1-2. doi: 10.1111/j.1528-1167.2011.02993.x. Review. No abstract available.

26.

Increased left parietal volumes relate to delayed language development in autism: a structural mri study.

Zoccante L, Viviani A, Ferro A, Cerini R, Cerruti S, Rambaldelli G, Bellani M, Dusi N, Perlini C, Boscaini F, Pozzi Mucelli R, Tansella M, Dalla Bernardina B, Brambilla P.

Funct Neurol. 2010 Oct-Dec;25(4):217-21.

PMID:
21388583
27.

Absence seizures in the first 3 years of life: an electroclinical study of 46 cases.

Caraballo RH, Darra F, Fontana E, Garcia R, Monese E, Dalla Bernardina B.

Epilepsia. 2011 Feb;52(2):393-400. doi: 10.1111/j.1528-1167.2010.02926.x. Epub 2011 Jan 26.

28.

Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.

Ragona F, Granata T, Dalla Bernardina B, Offredi F, Darra F, Battaglia D, Morbi M, Brazzo D, Cappelletti S, Chieffo D, De Giorgi I, Fontana E, Freri E, Marini C, Toraldo A, Specchio N, Veggiotti P, Vigevano F, Guerrini R, Guzzetta F, Dravet C.

Epilepsia. 2011 Feb;52(2):386-92. doi: 10.1111/j.1528-1167.2010.02925.x. Epub 2011 Jan 26.

29.

Infantile spams without hypsarrhythmia: a study of 16 cases.

Caraballo RH, Ruggieri V, Gonzalez G, Cersósimo R, Gamboni B, Rey A, Poveda JC, Dalla Bernardina B.

Seizure. 2011 Apr;20(3):197-202. doi: 10.1016/j.seizure.2010.11.018. Epub 2010 Dec 16.

30.

Infantile spasms: toward a selective diagnostic and therapeutic approach.

Dulac O, Bast T, Dalla Bernardina B, Gaily E, Neville B.

Epilepsia. 2010 Oct;51(10):2218-9; author reply 2221. doi: 10.1111/j.1528-1167.2010.02736.x. No abstract available.

31.

The relationship between body mass index and body size dissatisfaction in young adolescents: spline function analysis.

Cortese S, Falissard B, Pigaiani Y, Banzato C, Bogoni G, Pellegrino M, Vincenzi B, Angriman M, Cook S, Purper-Ouakil D, Dalla Bernardina B, Maffeis C.

J Am Diet Assoc. 2010 Jul;110(7):1098-102. doi: 10.1016/j.jada.2010.04.001.

PMID:
20630170
32.

Refining the phenotype associated with MEF2C haploinsufficiency.

Novara F, Beri S, Giorda R, Ortibus E, Nageshappa S, Darra F, Dalla Bernardina B, Zuffardi O, Van Esch H.

Clin Genet. 2010 Nov;78(5):471-7. doi: 10.1111/j.1399-0004.2010.01413.x.

PMID:
20412115
33.

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype.

van Bon BW, Koolen DA, Brueton L, McMullan D, Lichtenbelt KD, Adès LC, Peters G, Gibson K, Moloney S, Novara F, Pramparo T, Dalla Bernardina B, Zoccante L, Balottin U, Piazza F, Pecile V, Gasparini P, Guerci V, Kets M, Pfundt R, de Brouwer AP, Veltman JA, de Leeuw N, Wilson M, Antony J, Reitano S, Luciano D, Fichera M, Romano C, Brunner HG, Zuffardi O, de Vries BB.

Eur J Hum Genet. 2010 Feb;18(2):163-70. doi: 10.1038/ejhg.2009.152. Epub 2009 Oct 7. Erratum in: Eur J Hum Genet. 2010 Feb;18(2):170. Moloney, Susan [added]. Eur J Hum Genet. 2010 Oct;18(10):1171.

34.

Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.

Giorda R, Bonaglia MC, Beri S, Fichera M, Novara F, Magini P, Urquhart J, Sharkey FH, Zucca C, Grasso R, Marelli S, Castiglia L, Di Benedetto D, Musumeci SA, Vitello GA, Failla P, Reitano S, Avola E, Bisulli F, Tinuper P, Mastrangelo M, Fiocchi I, Spaccini L, Torniero C, Fontana E, Lynch SA, Clayton-Smith J, Black G, Jonveaux P, Leheup B, Seri M, Romano C, dalla Bernardina B, Zuffardi O.

Am J Hum Genet. 2009 Sep;85(3):394-400. doi: 10.1016/j.ajhg.2009.08.001. Epub 2009 Aug 27. Erratum in: Am J Hum Genet. 2009 Sep;85(3):419.

35.

Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children.

Vignoli A, Canevini MP, Darra F, La Selva L, Fiorini E, Piazzini A, Lazzarotto F, Zucca C, Dalla Bernardina B.

Epilepsia. 2009 Nov;50(11):2420-7. doi: 10.1111/j.1528-1167.2009.02176.x. Epub 2009 Jul 2.

36.

Benign myoclonus of early infancy or Fejerman syndrome.

Dalla Bernardina B.

Epilepsia. 2009 May;50(5):1290-2. doi: 10.1111/j.1528-1167.2009.02154.x. No abstract available.

37.

A study of 63 cases with eyelid myoclonia with or without absences: type of seizure or an epileptic syndrome?

Caraballo RH, Fontana E, Darra F, Chacon S, Ross N, Fiorini E, Fejerman N, Dalla Bernardina B.

Seizure. 2009 Jul;18(6):440-5. doi: 10.1016/j.seizure.2009.04.004. Epub 2009 May 5.

38.

Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria.

Artuso R, Mencarelli MA, Polli R, Sartori S, Ariani F, Pollazzon M, Marozza A, Cilio MR, Specchio N, Vigevano F, Vecchi M, Boniver C, Dalla Bernardina B, Parmeggiani A, Buoni S, Hayek G, Mari F, Renieri A, Murgia A.

Brain Dev. 2010 Jan;32(1):17-24. doi: 10.1016/j.braindev.2009.02.004. Epub 2009 Apr 10.

PMID:
19362436
39.

Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6.

Cannelli N, Garavaglia B, Simonati A, Aiello C, Barzaghi C, Pezzini F, Cilio MR, Biancheri R, Morbin M, Dalla Bernardina B, Granata T, Tessa A, Invernizzi F, Pessagno A, Boldrini R, Zibordi F, Grazian L, Claps D, Carrozzo R, Mole SE, Nardocci N, Santorelli FM.

Biochem Biophys Res Commun. 2009 Feb 20;379(4):892-7. doi: 10.1016/j.bbrc.2008.12.159. Epub 2009 Jan 7.

PMID:
19135028
40.

Benign nocturnal alternating hemiplegia of childhood: The first clinical report with paroxysmal events home-video recordings.

Sartori S, Vecchi M, Toldo I, Boniver C, Dalla Bernardina B, Maria Laverda A.

Mov Disord. 2008 Aug 15;23(11):1605-8. doi: 10.1002/mds.22180.

PMID:
18618665
41.

Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion.

Torniero C, Dalla Bernardina B, Novara F, Cerini R, Bonaglia C, Pramparo T, Ciccone R, Guerrini R, Zuffardi O.

Eur J Hum Genet. 2008 Aug;16(8):880-7. doi: 10.1038/ejhg.2008.42. Epub 2008 Mar 12.

42.

Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients.

Caraballo RH, Fontana E, Darra F, Cassar L, Negrini F, Fiorini E, Arroyo H, Ferraro S, Fejerman N, Dalla Bernardina B.

J Child Neurol. 2008 May;23(5):497-506. doi: 10.1177/0883073807309771. Epub 2008 Jan 29.

PMID:
18230844
43.

Parent reports of sleep/alertness problems and ADHD symptoms in a sample of obese adolescents.

Cortese S, Maffeis C, Konofal E, Lecendreux M, Comencini E, Angriman M, Vincenzi B, Pajno-Ferrara F, Mouren MC, Dalla Bernardina B.

J Psychosom Res. 2007 Dec;63(6):587-90.

PMID:
18061748
44.

Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13.

Torniero C, Zuffardi O, Darra F, Dalla Bernardina B.

Epilepsia. 2007 Nov;48(11):2177-80. Epub 2007 Jul 28.

45.

Attention-deficit/hyperactivity disorder, binge eating, and obesity.

Cortese S, Isnard P, Dalla Bernardina B, Mouren MC.

J Clin Psychiatry. 2007 Jun;68(6):976; author reply 976-7. No abstract available.

PMID:
17592935
46.

Does excessive daytime sleepiness contribute to explaining the association between obesity and ADHD symptoms?

Cortese S, Konofal E, Dalla Bernardina B, Mouren MC, Lecendreux M.

Med Hypotheses. 2008;70(1):12-6. Epub 2007 Jun 22.

PMID:
17587509
47.

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

Striano P, Mancardi MM, Biancheri R, Madia F, Gennaro E, Paravidino R, Beccaria F, Capovilla G, Dalla Bernardina B, Darra F, Elia M, Giordano L, Gobbi G, Granata T, Ragona F, Guerrini R, Marini C, Mei D, Longaretti F, Romeo A, Siri L, Specchio N, Vigevano F, Striano S, Tortora F, Rossi A, Minetti C, Dravet C, Gaggero R, Zara F.

Epilepsia. 2007 Jun;48(6):1092-6. Epub 2007 Mar 22.

48.

Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus.

Torniero C, dalla Bernardina B, Novara F, Vetro A, Ricca I, Darra F, Pramparo T, Guerrini R, Zuffardi O.

Eur J Hum Genet. 2007 Jan;15(1):62-7. Epub 2006 Oct 31.

49.

Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.

Mancardi MM, Striano P, Gennaro E, Madia F, Paravidino R, Scapolan S, Dalla Bernardina B, Bertini E, Bianchi A, Capovilla G, Darra F, Elia M, Freri E, Gobbi G, Granata T, Guerrini R, Pantaleoni C, Parmeggiani A, Romeo A, Santucci M, Vecchi M, Veggiotti P, Vigevano F, Pistorio A, Gaggero R, Zara F.

Epilepsia. 2006 Oct;47(10):1629-35. Erratum in: Epilepsia. 2007 Feb;48(2):409.

50.

Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.

Russo S, Finelli P, Recalcati MP, Ferraiuolo S, Cogliati F, Dalla Bernardina B, Tibiletti MG, Agosti M, Sala M, Bonati MT, Larizza L.

J Med Genet. 2006 Aug;43(8):e39.

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