Duro G - Search Results

1

Germline mosaicism for the c.2021G > A (p.Arg674Gln) mutation in siblings with trismus pseudocamptodactyly.

Bonapace G, Ceravolo F, Piccirillo A, Duro G, Strisciuglio P, Concolino D. Bonapace G, et al. Among authors: duro g. Am J Med Genet A. 2010 Nov;152A(11):2898-900. doi: 10.1002/ajmg.a.33671. Am J Med Genet A. 2010. PMID: 20949528 No abstract available.

2

Misdiagnosis of familial Mediterranean fever in patients with Anderson-Fabry disease.

Zizzo C, Colomba P, Albeggiani G, Gallizzi R, Iemolo F, Nuzzo D, Vasto S, Caruso C, Duro G. Zizzo C, et al. Among authors: duro g. Clin Genet. 2013 Jun;83(6):576-81. doi: 10.1111/j.1399-0004.2012.01940.x. Epub 2012 Aug 20. Clin Genet. 2013. PMID: 22905681

3

High variability of Fabry disease manifestations in an extended Italian family.

Cammarata G, Fatuzzo P, Rodolico MS, Colomba P, Sicurella L, Iemolo F, Zizzo C, Alessandro R, Bartolotta C, Duro G, Monte I. Cammarata G, et al. Among authors: duro g. Biomed Res Int. 2015;2015:504784. doi: 10.1155/2015/504784. Epub 2015 Apr 22. Biomed Res Int. 2015. PMID: 25977923 Free PMC article.

4

A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report.

Pisani A, Imbriaco M, Zizzo C, Albeggiani G, Colomba P, Alessandro R, Iemolo F, Duro G. Pisani A, et al. Among authors: duro g. BMC Cardiovasc Disord. 2012 Jun 8;12:39. doi: 10.1186/1471-2261-12-39. BMC Cardiovasc Disord. 2012. PMID: 22682330 Free PMC article.

5

Novel α-galactosidase A mutation in patients with severe cardiac manifestations of Fabry disease.

Duro G, Musumeci MB, Colomba P, Zizzo C, Albeggiani G, Mastromarino V, Volpe M, Autore C. Duro G, et al. Gene. 2014 Feb 10;535(2):365-9. doi: 10.1016/j.gene.2013.09.058. Epub 2013 Oct 17. Gene. 2014. PMID: 24140492

6

De novo mutation in a male patient with Fabry disease: a case report.

Iemolo F, Pizzo F, Albeggiani G, Zizzo C, Colomba P, Scalia S, Bartolotta C, Duro G. Iemolo F, et al. Among authors: duro g. BMC Res Notes. 2014 Jan 7;7:11. doi: 10.1186/1756-0500-7-11. BMC Res Notes. 2014. PMID: 24398019 Free PMC article.

7

A family with various symptomatology suggestive of Anderson-Fabry disease and a genetic polymorphism of alpha galactosidase A gene.

Tuttolomondo A, Duro G, Pecoraro R, Simonetta I, Miceli S, Colomba P, Zizzo C, Di Chiara T, Scaglione R, Della Corte V, Corpora F, Pinto A. Tuttolomondo A, et al. Among authors: duro g. Clin Biochem. 2015 Jan;48(1-2):55-62. doi: 10.1016/j.clinbiochem.2014.09.018. Epub 2014 Oct 2. Clin Biochem. 2015. PMID: 25281798

8

Response to Simsek et al.

Duro G, Zizzo C, Colomba P. Duro G, et al. Clin Genet. 2013 Jun;83(6):584. doi: 10.1111/cge.12134. Epub 2013 Apr 5. Clin Genet. 2013. PMID: 23557189 No abstract available.

9

Molecular and clinical studies in five index cases with novel mutations in the GLA gene.

Zizzo C, Monte I, Pisani A, Fatuzzo P, Riccio E, Rodolico MS, Colomba P, Uva M, Cammarata G, Alessandro R, Iemolo F, Duro G. Zizzo C, et al. Among authors: duro g. Gene. 2016 Mar 1;578(1):100-4. doi: 10.1016/j.gene.2015.12.024. Epub 2015 Dec 12. Gene. 2016. PMID: 26691501

10

Inter-familial and intra-familial phenotypic variability in three Sicilian families with Anderson-Fabry disease.

Tuttolomondo A, Simonetta I, Duro G, Pecoraro R, Miceli S, Colomba P, Zizzo C, Nucera A, Daidone M, Di Chiara T, Scaglione R, Della Corte V, Corpora F, Vogiatzis D, Pinto A. Tuttolomondo A, et al. Among authors: duro g. Oncotarget. 2017 May 29;8(37):61415-61424. doi: 10.18632/oncotarget.18250. eCollection 2017 Sep 22. Oncotarget. 2017. PMID: 28977874 Free PMC article.

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