Moretti E - Search Results

1

Treatment with L-arginine improves neuropsychological disorders in a child with creatine transporter defect.

Chilosi A, Leuzzi V, Battini R, Tosetti M, Ferretti G, Comparini A, Casarano M, Moretti E, Alessandri MG, Bianchi MC, Cioni G. Chilosi A, et al. Among authors: moretti e. Neurocase. 2008;14(2):151-61. doi: 10.1080/13554790802060821. Neurocase. 2008. PMID: 18569740

2

A proposed multidisciplinary approach for identifying feeding abnormalities in children with cerebral palsy.

Santoro A, Lang MB, Moretti E, Sellari-Franceschini S, Orazini L, Cipriani P, Cioni G, Battini R. Santoro A, et al. Among authors: moretti e. J Child Neurol. 2012 Jun;27(6):708-12. doi: 10.1177/0883073811424083. Epub 2011 Oct 21. J Child Neurol. 2012. PMID: 22019841

3

Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.

Casarano M, Alessandrì MG, Salomons GS, Moretti E, Jakobs C, Gibson KM, Cioni G, Battini R. Casarano M, et al. Among authors: moretti e. JIMD Rep. 2012;2:119-23. doi: 10.1007/8904_2011_60. Epub 2011 Sep 6. JIMD Rep. 2012. PMID: 23430864 Free PMC article.

4

Infantile-Onset Pompe Disease: The Care Beyond the Cure.

Astrea G, Perazza S, Frosini S, Moretti E, Sacchini M, Dati E, Pecini C, Procopio E, Santorelli FM, Donati MA, Battini R. Astrea G, et al. Among authors: moretti e. J Neuromuscul Dis. 2015;2(s1):S58-S59. J Neuromuscul Dis. 2015. PMID: 27858649 No abstract available.

5

Learning disabilities in neuromuscular disorders: a springboard for adult life.

Astrea G, Battini R, Lenzi S, Frosini S, Bonetti S, Moretti E, Perazza S, Santorelli FM, Pecini C. Astrea G, et al. Among authors: moretti e. Acta Myol. 2016 Oct;35(2):90-95. Acta Myol. 2016. PMID: 28344438 Free PMC article. Review.

6

Lung ultrasound in young children with neurological impairment: A proposed integrative clinical tool for deaeration-detection related to feeding.

Fiori S, Moretti E, Amador C, Martinelli A, Scaramuzzo RT, Controzzi T, Battini R, Filippi L, Guzzetta A, Gargani L. Fiori S, et al. Among authors: moretti e. Front Pediatr. 2022 Jul 27;10:932409. doi: 10.3389/fped.2022.932409. eCollection 2022. Front Pediatr. 2022. PMID: 35967558 Free PMC article.

7

6p25 interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder.

Bozza M, Bernardini L, Novelli A, Brovedani P, Moretti E, Canapicchi R, Doccini V, Filippi T, Battaglia A. Bozza M, et al. Among authors: moretti e. Eur J Paediatr Neurol. 2013 May;17(3):225-31. doi: 10.1016/j.ejpn.2012.09.008. Epub 2012 Oct 12. Eur J Paediatr Neurol. 2013. PMID: 23069351 Review.

8

LUNCH-Lung Ultrasound for early detection of silent and apparent aspiratioN in infants and young CHildren with cerebral palsy and other developmental disabilities: study protocol of a randomized controlled trial.

Fiori S, Scaramuzzo RT, Moretti E, Amador C, Controzzi T, Martinelli A, Filippi L, Guzzetta A, Gargagni L. Fiori S, et al. Among authors: moretti e. BMC Pediatr. 2022 Jun 23;22(1):360. doi: 10.1186/s12887-022-03413-z. BMC Pediatr. 2022. PMID: 35739502 Free PMC article.

9

A novel deletion in exon 12 (g1845delAG or g1846delGA) of the CFTR (ABCC7) gene in a CF infant presenting with meconium ileus.

Seia M, Cantù-Rajnoldi A, Ambrosioni A, Fiori S, Prandoni S, Corbetta C, Bassotti A, Moretti E, Giunta A, Padoan R. Seia M, et al. Among authors: moretti e. Hum Mutat. 2000 Sep;16(3):279. doi: 10.1002/1098-1004(200009)16:3<279::AID-HUMU31>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10980555 No abstract available.

10

Otorhinolaringologic manifestation of Smith-Magenis syndrome.

Di Cicco M, Padoan R, Felisati G, Dilani D, Moretti E, Guerneri S, Selicorni A. Di Cicco M, et al. Among authors: moretti e. Int J Pediatr Otorhinolaryngol. 2001 Jun 7;59(2):147-50. doi: 10.1016/s0165-5876(01)00475-x. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11378192

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