Andria G - Search Results

1

[Anderson-Fabry's disease: diagnostic problems, therapeutic relevance, and clinical experience in the treatment of the disease with enzyme replacement therapy in nephropathic patients].

Cianciaruso B, Pisani A, Andreucci MV, Parente N, Andria G, Federico S, Sabbatini M, Sessa A. Cianciaruso B, et al. Among authors: andria g. G Ital Nefrol. 2003 Mar-Apr;20(2):113-9. G Ital Nefrol. 2003. PMID: 12746795 Review. Italian.

2

Synergy between the pharmacological chaperone 1-deoxygalactonojirimycin and the human recombinant alpha-galactosidase A in cultured fibroblasts from patients with Fabry disease.

Porto C, Pisani A, Rosa M, Acampora E, Avolio V, Tuzzi MR, Visciano B, Gagliardo C, Materazzi S, la Marca G, Andria G, Parenti G. Porto C, et al. Among authors: andria g. J Inherit Metab Dis. 2012 May;35(3):513-20. doi: 10.1007/s10545-011-9424-3. Epub 2011 Dec 21. J Inherit Metab Dis. 2012. PMID: 22187137

3

Synergy between the pharmacological chaperone 1-deoxygalactonojirimycin and agalsidase alpha in cultured fibroblasts from patients with Fabry disease.

Pisani A, Porto C, Andria G, Parenti G. Pisani A, et al. Among authors: andria g. J Inherit Metab Dis. 2014 Jan;37(1):145-6. doi: 10.1007/s10545-013-9641-z. Epub 2013 Aug 22. J Inherit Metab Dis. 2014. PMID: 23974650 No abstract available.

4

Unbalanced translocation (3;5)(q26.1;p14): a clinical report.

Rossi M, Di Micco P, Perone L, De Brasi D, Guzzetta V, Andreucci MV, Vega GR, Marzano MG, Iaccarino E, Andria G. Rossi M, et al. Among authors: andria g. Am J Med Genet. 2002 Jul 15;110(4):353-8. doi: 10.1002/ajmg.10440. Am J Med Genet. 2002. PMID: 12116209 Review.

5

X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability.

Brunetti-Pierri N, Andreucci MV, Tuzzi R, Vega GR, Gray G, McKeown C, Ballabio A, Andria G, Meroni G, Parenti G. Brunetti-Pierri N, et al. Among authors: andria g. Am J Med Genet A. 2003 Mar 1;117A(2):164-8. doi: 10.1002/ajmg.a.10950. Am J Med Genet A. 2003. PMID: 12567415

6

Upper airway obstructive disease in mucopolysaccharidoses: polysomnography, computed tomography and nasal endoscopy findings.

Santamaria F, Andreucci MV, Parenti G, Polverino M, Viggiano D, Montella S, Cesaro A, Ciccarelli R, Capaldo B, Andria G. Santamaria F, et al. Among authors: andria g. J Inherit Metab Dis. 2007 Oct;30(5):743-9. doi: 10.1007/s10545-007-0555-5. Epub 2007 Jun 14. J Inherit Metab Dis. 2007. PMID: 17570075

7

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.

8

The pharmacological chaperone N-butyldeoxynojirimycin enhances enzyme replacement therapy in Pompe disease fibroblasts.

Porto C, Cardone M, Fontana F, Rossi B, Tuzzi MR, Tarallo A, Barone MV, Andria G, Parenti G. Porto C, et al. Among authors: andria g. Mol Ther. 2009 Jun;17(6):964-71. doi: 10.1038/mt.2009.53. Epub 2009 Mar 17. Mol Ther. 2009. PMID: 19293774 Free PMC article.

9

Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study.

Melis D, Parenti G, Gatti R, Casa RD, Parini R, Riva E, Burlina AB, Dionisi Vici C, Di Rocco M, Furlan F, Torcoletti M, Papadia F, Donati A, Benigno V, Andria G. Melis D, et al. Among authors: andria g. Clin Endocrinol (Oxf). 2005 Jul;63(1):19-25. doi: 10.1111/j.1365-2265.2005.02292.x. Clin Endocrinol (Oxf). 2005. PMID: 15963056

10

Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry.

Limongelli G, Iucolano S, Monda E, Elefante P, De Stasio C, Lubrano I, Caiazza M, Mazzella M, Fimiani F, Galdo M, De Marchi G, Esposito M, Rubino M, Cirillo A, Fusco A, Esposito A, Trama U, Esposito S, Scarano G, Sepe J, Andria G, Orlando V, Menditto E, Chiodini P; Campania Rare Disease Network. Limongelli G, et al. Among authors: andria g. J Public Health (Oxf). 2022 Aug 25;44(3):586-594. doi: 10.1093/pubmed/fdab137. J Public Health (Oxf). 2022. PMID: 33982102 Free PMC article.

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