Iorio R - Search Results

1

Rare variants in PKHD1 associated with Caroli syndrome: Two case reports.

Giacobbe C, Di Dato F, Palma D, Amitrano M, Iorio R, Fortunato G. Giacobbe C, et al. Among authors: iorio r. Mol Genet Genomic Med. 2022 Aug;10(8):e1998. doi: 10.1002/mgg3.1998. Epub 2022 Jun 17. Mol Genet Genomic Med. 2022. PMID: 35715958 Free PMC article.

2

Macroenzyme investigation and monitoring in children with persistent increase of aspartate aminotransferase of unexplained origin.

Fortunato G, Iorio R, Esposito P, Lofrano MM, Vegnente A, Vajro P. Fortunato G, et al. Among authors: iorio r. J Pediatr. 1998 Aug;133(2):286-9. doi: 10.1016/s0022-3476(98)70238-0. J Pediatr. 1998. PMID: 9709724

3

Prevalence and long-term course of macro-aspartate aminotransferase in children.

Caropreso M, Fortunato G, Lenta S, Palmieri D, Esposito M, Vitale DF, Iorio R, Vajro P. Caropreso M, et al. Among authors: iorio r. J Pediatr. 2009 May;154(5):744-8. doi: 10.1016/j.jpeds.2008.11.010. Epub 2008 Dec 25. J Pediatr. 2009. PMID: 19111320

4

Ultrasound scanning in infants with biliary atresia: the different implications of biliary tract features and liver echostructure.

Iorio R, Liccardo D, Di Dato F, Puoti MG, Spagnuolo MI, Alberti D, Vallone G. Iorio R, et al. Ultraschall Med. 2013 Oct;34(5):463-7. doi: 10.1055/s-0033-1335455. Epub 2013 May 21. Ultraschall Med. 2013. PMID: 23696064

5

Zinc monotherapy is effective in Wilson's disease patients with mild liver disease diagnosed in childhood: a retrospective study.

Ranucci G, Di Dato F, Spagnuolo MI, Vajro P, Iorio R. Ranucci G, et al. Among authors: iorio r. Orphanet J Rare Dis. 2014 Mar 25;9:41. doi: 10.1186/1750-1172-9-41. Orphanet J Rare Dis. 2014. PMID: 24661374 Free PMC article.

6

Penicillamine-induced Elastosis Perforans Serpiginosa in Wilson Disease: Is Useful Switching to Zinc?

Ranucci G, Di Dato F, Leone F, Vajro P, Spagnuolo MI, Iorio R. Ranucci G, et al. Among authors: iorio r. J Pediatr Gastroenterol Nutr. 2017 Mar;64(3):e72-e73. doi: 10.1097/MPG.0000000000000613. J Pediatr Gastroenterol Nutr. 2017. PMID: 25341025 No abstract available.

7

Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene.

Mameli E, Lepori MB, Chiappe F, Ranucci G, Di Dato F, Iorio R, Loudianos G. Mameli E, et al. Among authors: iorio r. Gene. 2015 Sep 15;569(2):276-9. doi: 10.1016/j.gene.2015.05.067. Epub 2015 May 30. Gene. 2015. PMID: 26031236

8

A retrospective evaluation of the association of celiac disease and growth hormone deficiency: more than a casual association?

Giannattasio A, DI Dato F, Minicucci V, Mariano M, Spagnuolo MI, Macchiaroli A, Iorio R. Giannattasio A, et al. Among authors: iorio r. Minerva Endocrinol. 2017 Mar;42(1):24-29. doi: 10.23736/S0391-1977.16.02366-X. Epub 2015 Oct 23. Minerva Endocrinol. 2017. PMID: 26496658

9

Subclinical neurological involvement does not develop if Wilson's disease is treated early.

Dubbioso R, Ranucci G, Esposito M, Di Dato F, Topa A, Quarantelli M, Matarazzo M, Santoro L, Manganelli F, Iorio R. Dubbioso R, et al. Among authors: iorio r. Parkinsonism Relat Disord. 2016 Mar;24:15-9. doi: 10.1016/j.parkreldis.2016.01.024. Epub 2016 Jan 29. Parkinsonism Relat Disord. 2016. PMID: 26851839

10

Tubercular hemoptysis in a young liver transplanted patient: Case report.

Di Dato F, Nunziata F, Rosa M, Iorio R, Spagnuolo MI. Di Dato F, et al. Among authors: iorio r. Medicine (Baltimore). 2019 Aug;98(33):e16761. doi: 10.1097/MD.0000000000016761. Medicine (Baltimore). 2019. PMID: 31415374 Free PMC article.

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