Romano A - Search Results

1

Electroencephalographic findings in ATRX syndrome: A new case series and review of literature.

Aiello S, Mancardi MM, Romano A, Santucci M, Scaduto MC, Vari MS, Striano P, Operto FF, Elia M, Vitiello G, Del Giudice E, Terrone G. Aiello S, et al. Among authors: romano a. Eur J Paediatr Neurol. 2022 Sep;40:69-72. doi: 10.1016/j.ejpn.2022.08.002. Epub 2022 Aug 18. Eur J Paediatr Neurol. 2022. PMID: 36031702 Review.

2

EEG findings in West syndrome a follow-up of 20 patients.

Vacca G, de Falco FA, Natale S, del Giudice E, Romano A, Latte F, Bianchi L. Vacca G, et al. Among authors: romano a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):297-303. Acta Neurol (Napoli). 1992. PMID: 1338179

3

Megalocornea and mental retardation syndrome: two new cases.

Del Giudice E, Sartorio R, Romano A, Carrozzo R, Andria G. Del Giudice E, et al. Among authors: romano a. Am J Med Genet. 1987 Feb;26(2):417-20. doi: 10.1002/ajmg.1320260220. Am J Med Genet. 1987. PMID: 3812592

4

Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.

Curatolo P, Cilio MR, Del Giudice E, Romano A, Gaggero R, Pessagno A. Curatolo P, et al. Among authors: romano a. Neuropediatrics. 1993 Apr;24(2):77-82. doi: 10.1055/s-2008-1071518. Neuropediatrics. 1993. PMID: 8327066

5

Short duration outpatient video electroencephalographic monitoring: the experience of a southern-Italian general pediatric department.

Del Giudice E, Crisanti AF, Romano A. Del Giudice E, et al. Among authors: romano a. Epileptic Disord. 2002 Sep;4(3):197-202. Epileptic Disord. 2002. PMID: 12446222 Free article.

6

Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.

Del Giudice E, Savoldi G, Notarangelo LD, Di Benedetto L, Manganelli F, Bruzzese E, Romano A, Santoro L. Del Giudice E, et al. Among authors: romano a. Acta Paediatr. 2003;92(3):398-401. Acta Paediatr. 2003. PMID: 12725560

7

Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.

Titomanlio L, Romano A, Conti A, Genesio R, Salerno M, De Brasi D, Nitsch L, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Am J Med Genet A. 2004 Jun 1;127A(2):197-200. doi: 10.1002/ajmg.a.20667. Am J Med Genet A. 2004. PMID: 15108211

8

Cerebellar agenesis.

Titomanlio L, Romano A, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Neurology. 2005 Mar 22;64(6):E21. doi: 10.1212/wnl.64.6.e21. Neurology. 2005. PMID: 15781801 No abstract available.

9

Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome.

Titomanlio L, De Brasi D, Romano A, Genesio R, Diano AA, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Acta Paediatr. 2006 Jul;95(7):861-3. doi: 10.1080/08035250500527307. Acta Paediatr. 2006. PMID: 16801186

10

Impact of malnutrition on gastrointestinal disorders and gross motor abilities in children with cerebral palsy.

Campanozzi A, Capano G, Miele E, Romano A, Scuccimarra G, Del Giudice E, Strisciuglio C, Militerni R, Staiano A. Campanozzi A, et al. Among authors: romano a. Brain Dev. 2007 Jan;29(1):25-9. doi: 10.1016/j.braindev.2006.05.008. Epub 2006 Jul 14. Brain Dev. 2007. PMID: 16843628

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