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Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus.
Ital J Pediatr. 2022 Jul 19;48(1):118. doi: 10.1186/s13052-022-01312-8.
Ital J Pediatr. 2022.
PMID: 35854335
Free PMC article.
Aromatic L-amino Acid Decarboxylase (AADC) deficiency: results from an Italian modified Delphi consensus.
Fusco C, Leuzzi V, Striano P, Battini R, Burlina A; Delphi panel experts’ group; Spagnoli C.
Fusco C, et al.
Ital J Pediatr. 2021 Jan 21;47(1):13. doi: 10.1186/s13052-021-00954-4.
Ital J Pediatr. 2021.
PMID: 33478565
Free PMC article.
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The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein.
Laforgia N, De Cosmo L, Palumbo O, Ranieri C, Sesta M, Capodiferro D, Pantaleo A, Iapicca P, Lastella P, Capozza M, Schettini F, Bukvic N, Bagnulo R, Resta N.
Laforgia N, et al. Among authors: capodiferro d.
Genes (Basel). 2020 Dec 18;11(12):1519. doi: 10.3390/genes11121519.
Genes (Basel). 2020.
PMID: 33353066
Free PMC article.
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De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly.
Resta N, De Cosmo L, Susca FC, Capodiferro D, Nardone AM, Pastorivo D, Bertoli M, Serlenga C, Burattini M, Schettini F, Laforgia N.
Resta N, et al. Among authors: capodiferro d.
Am J Med Genet A. 2013 Mar;161A(3):632-6. doi: 10.1002/ajmg.a.35777. Epub 2013 Feb 7.
Am J Med Genet A. 2013.
PMID: 23401394
No abstract available.
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Unlicensed and off-label use of medicines at a neonatology clinic in Italy.
Dell'Aera M, Gasbarro AR, Padovano M, Laforgia N, Capodiferro D, Solarino B, Quaranta R, Dell'Erba AS.
Dell'Aera M, et al. Among authors: capodiferro d.
Pharm World Sci. 2007 Aug;29(4):361-7. doi: 10.1007/s11096-006-9081-z. Epub 2007 Mar 10.
Pharm World Sci. 2007.
PMID: 17351821
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Classic Galactosemia: Clinical and Computational Characterization of a Novel GALT Missense Variant (p.A303D) and a Literature Review.
Forte G, Buonadonna AL, Pantaleo A, Fasano C, Capodiferro D, Grossi V, Sanese P, Cariola F, De Marco K, Lepore Signorile M, Manghisi A, Guglielmi AF, Simonetti S, Laforgia N, Disciglio V, Simone C.
Forte G, et al. Among authors: capodiferro d.
Int J Mol Sci. 2023 Dec 12;24(24):17388. doi: 10.3390/ijms242417388.
Int J Mol Sci. 2023.
PMID: 38139222
Free PMC article.
Review.
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Long-term enzyme replacement therapy in a severe case of mucopolysaccharidosis type II (Hunter syndrome).
Papadia F, Lozupone MS, Gaeta A, Capodiferro D, Lacalendola G.
Papadia F, et al. Among authors: capodiferro d.
Eur Rev Med Pharmacol Sci. 2011 Mar;15(3):253-8.
Eur Rev Med Pharmacol Sci. 2011.
PMID: 21528770
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