Andria G - Search Results

1

Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment.

Rosa M, Pascarella A, Parenti G, Buono S, Romano A, Della Casa R, Andria G, Marino M, Riccio MP, Bravaccio C. Rosa M, et al. Among authors: andria g. Eur J Paediatr Neurol. 2012 Mar;16(2):203-5. doi: 10.1016/j.ejpn.2011.07.003. Epub 2011 Aug 24. Eur J Paediatr Neurol. 2012. PMID: 21868270

2

Universal screening for inherited metabolic diseases in the neonate (and the fetus).

Scala I, Parenti G, Andria G. Scala I, et al. Among authors: andria g. J Matern Fetal Neonatal Med. 2012 Oct;25(Suppl 5):4-6. doi: 10.3109/14767058.2012.716983. J Matern Fetal Neonatal Med. 2012. PMID: 23025760 Free article. Review.

3

Long-term enzyme replacement therapy for pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells.

Rossi M, Parenti G, Della Casa R, Romano A, Mansi G, Agovino T, Rosapepe F, Vosa C, Del Giudice E, Andria G. Rossi M, et al. Among authors: andria g. J Child Neurol. 2007 May;22(5):565-73. doi: 10.1177/0883073807302598. J Child Neurol. 2007. PMID: 17690063 Clinical Trial.

4

Pompe disease: from new views on pathophysiology to innovative therapeutic strategies.

Parenti G, Andria G. Parenti G, et al. Among authors: andria g. Curr Pharm Biotechnol. 2011 Jun;12(6):902-15. doi: 10.2174/138920111795542606. Curr Pharm Biotechnol. 2011. PMID: 21235442

5

The videofluoroscopic swallowing study shows a sustained improvement of dysphagia in children with Niemann-Pick disease type C after therapy with miglustat.

Fecarotta S, Amitrano M, Romano A, Della Casa R, Bruschini D, Astarita L, Parenti G, Andria G. Fecarotta S, et al. Among authors: andria g. Am J Med Genet A. 2011 Mar;155A(3):540-7. doi: 10.1002/ajmg.a.33847. Epub 2011 Feb 22. Am J Med Genet A. 2011. PMID: 21344635

6

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation.

Fecarotta S, Parenti G, Vajro P, Zuppaldi A, Della Casa R, Carbone MT, Correra A, Torre G, Riva S, Dionisi-Vici C, Santorelli FM, Andria G. Fecarotta S, et al. Among authors: andria g. J Inherit Metab Dis. 2006 Feb;29(1):186-9. doi: 10.1007/s10545-006-0120-7. J Inherit Metab Dis. 2006. PMID: 16601889

7

Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report.

Fecarotta S, Gragnaniello V, Della Casa R, Romano A, Raiano E, Torella A, Savarese M, Nigro V, Strisciuglio P, Andria G, Parenti G. Fecarotta S, et al. Among authors: andria g. Neuromuscul Disord. 2018 Nov;28(11):956-960. doi: 10.1016/j.nmd.2018.07.001. Epub 2018 Jul 19. Neuromuscul Disord. 2018. PMID: 30126629

8

Pharmacological Chaperone Therapy: Preclinical Development, Clinical Translation, and Prospects for the Treatment of Lysosomal Storage Disorders.

Parenti G, Andria G, Valenzano KJ. Parenti G, et al. Among authors: andria g. Mol Ther. 2015 Jul;23(7):1138-1148. doi: 10.1038/mt.2015.62. Epub 2015 Apr 16. Mol Ther. 2015. PMID: 25881001 Free PMC article. Review.

9

Isovaleric acidemia.

Pascarella A, Rosa M, della Casa R, Andria G, Parenti G. Pascarella A, et al. Among authors: andria g. J Pediatr Endocrinol Metab. 2011;24(5-6):399. J Pediatr Endocrinol Metab. 2011. PMID: 21823546 No abstract available.

10

Respiratory manifestations in patients with inherited metabolic diseases.

Santamaria F, Montella S, Mirra V, De Stefano S, Andria G, Parenti G. Santamaria F, et al. Among authors: andria g. Eur Respir Rev. 2013 Dec;22(130):437-53. doi: 10.1183/09059180.00008012. Eur Respir Rev. 2013. PMID: 24293461 Free PMC article. Review.

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