Giordano L - Search Results

1

Cognitive improvement after cochlear implantation in deaf children with associated disabilities.

Micheletti S, Accorsi P, Giordano L, Calza S, Nassif N, Barezzani MG, Fazzi E, Redaelli de Zinis LO. Micheletti S, et al. Among authors: giordano l. Dev Med Child Neurol. 2020 Dec;62(12):1429-1436. doi: 10.1111/dmcn.14671. Epub 2020 Sep 11. Dev Med Child Neurol. 2020. PMID: 32914885 Free article.

2

Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.

Giordano L, Accorsi P, Valseriati D, Tiberti A, Menegati E, Zara F, Vignoli A, Vigevano F. Giordano L, et al. Neuropediatrics. 1999 Apr;30(2):99-101. doi: 10.1055/s-2007-973469. Neuropediatrics. 1999. PMID: 10401694

3

Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literature.

Capovilla G, Lorenzetti ME, Montagnini A, Borgatti R, Piccinelli P, Giordano L, Accorsi P, Caudana R. Capovilla G, et al. Among authors: giordano l. J Child Neurol. 2001 May;16(5):382-6. doi: 10.1177/088307380101600516. J Child Neurol. 2001. PMID: 11392528

4

Crisponi syndrome: report of a further patient.

Accorsi P, Giordano L, Faravelli F. Accorsi P, et al. Among authors: giordano l. Am J Med Genet A. 2003 Dec 1;123A(2):183-5. doi: 10.1002/ajmg.a.20292. Am J Med Genet A. 2003. PMID: 14598344

5

Favorable outcome of cochlear implant in VIIIth nerve deficiency.

Zanetti D, Guida M, Barezzani MG, Campovecchi C, Nassif N, Pinelli L, Giordano L, Olioso G. Zanetti D, et al. Among authors: giordano l. Otol Neurotol. 2006 Sep;27(6):815-23. doi: 10.1097/01.mao.0000227899.80656.1d. Otol Neurotol. 2006. PMID: 16936567

6

Celiac disease-related antibodies in Italian children with epilepsy.

Giordano L, Valotti M, Bosetti A, Accorsi P, Caimi L, Imberti L. Giordano L, et al. Pediatr Neurol. 2009 Jul;41(1):34-6. doi: 10.1016/j.pediatrneurol.2009.02.009. Pediatr Neurol. 2009. PMID: 19520271

7

Joubert syndrome with bilateral polymicrogyria: clinical and neuropathological findings in two brothers.

Giordano L, Vignoli A, Pinelli L, Brancati F, Accorsi P, Faravelli F, Gasparotti R, Granata T, Giaccone G, Inverardi F, Frassoni C, Dallapiccola B, Valente EM, Spreafico R. Giordano L, et al. Am J Med Genet A. 2009 Jul;149A(7):1511-5. doi: 10.1002/ajmg.a.32936. Am J Med Genet A. 2009. PMID: 19533793

8

Congenital systematized basaloid follicular hamartoma with microphthalmia and hemimegalencephaly.

Boccaletti V, Accorsi P, Pinelli L, Ungari M, Giordano L, Neri I, De Panfilis G. Boccaletti V, et al. Among authors: giordano l. Pediatr Dermatol. 2011 Sep-Oct;28(5):555-60. doi: 10.1111/j.1525-1470.2010.01225.x. Epub 2010 Nov 9. Pediatr Dermatol. 2011. PMID: 21062348

9

Familial Ohtahara syndrome due to a novel ARX gene mutation.

Giordano L, Sartori S, Russo S, Accorsi P, Galli J, Tiberti A, Bettella E, Marchi M, Vignoli A, Darra F, Murgia A, Bernardina BD. Giordano L, et al. Am J Med Genet A. 2010 Dec;152A(12):3133-7. doi: 10.1002/ajmg.a.33701. Am J Med Genet A. 2010. PMID: 21108397 Free article.

10

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. Sartori S, et al. Among authors: giordano l. J Child Neurol. 2011 Jun;26(6):683-91. doi: 10.1177/0883073810387827. Epub 2011 Apr 11. J Child Neurol. 2011. PMID: 21482751

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