Biolcati G - Search Results

1

In ferrochelatase-deficient protoporphyria patients, ALAS2 expression is enhanced and erythrocytic protoporphyrin concentration correlates with iron availability.

Barman-Aksözen J, Minder EI, Schubiger C, Biolcati G, Schneider-Yin X. Barman-Aksözen J, et al. Among authors: biolcati g. Blood Cells Mol Dis. 2015 Jan;54(1):71-7. doi: 10.1016/j.bcmd.2014.07.017. Epub 2014 Aug 30. Blood Cells Mol Dis. 2015. PMID: 25179834 Clinical Trial.

2

Heterogeneity of mutations in the ferrochelatase gene in Italian patients with erythropoietic protoporphyria.

Aurizi C, Schneider-Yin X, Sorge F, Macrì A, Minder EI, Biolcati G. Aurizi C, et al. Among authors: biolcati g. Mol Genet Metab. 2007 Apr;90(4):402-7. doi: 10.1016/j.ymgme.2006.10.012. Epub 2006 Dec 29. Mol Genet Metab. 2007. PMID: 17196862

3

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.

Barman-Aksoezen J, Girelli D, Aurizi C, Schneider-Yin X, Campostrini N, Barbieri L, Minder EI, Biolcati G. Barman-Aksoezen J, et al. Among authors: biolcati g. J Inherit Metab Dis. 2017 May;40(3):433-441. doi: 10.1007/s10545-017-0017-7. Epub 2017 Feb 9. J Inherit Metab Dis. 2017. PMID: 28185024

4

Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria.

Biolcati G, Marchesini E, Sorge F, Barbieri L, Schneider-Yin X, Minder EI. Biolcati G, et al. Br J Dermatol. 2015 Jun;172(6):1601-1612. doi: 10.1111/bjd.13598. Epub 2015 Apr 30. Br J Dermatol. 2015. PMID: 25494545 Clinical Trial.

5

Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL.

Biolcati G, Hanneken S, Minder EI, Neumann NJ, Wilson JHP, Wolgen PJ, Wright DJ, Lloyd AJ. Biolcati G, et al. J Patient Rep Outcomes. 2021 Aug 3;5(1):65. doi: 10.1186/s41687-021-00345-7. J Patient Rep Outcomes. 2021. PMID: 34342778 Free PMC article.

6

Correction to: Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL.

Biolcati G, Hanneken S, Minder EI, Neumann NJ, Wilson JHP, Wolgen PJ, Wright DJ, Lloyd AJ. Biolcati G, et al. J Patient Rep Outcomes. 2021 Aug 15;5(1):73. doi: 10.1186/s41687-021-00348-4. J Patient Rep Outcomes. 2021. PMID: 34396462 Free PMC article. No abstract available.

7

Erythropoietic protoporphyria in a boy.

Buonuomo PS, Macchiaiolo M, Gonfiantini MV, Biolcati G, Pitisci A, Villani A, Bartuli A. Buonuomo PS, et al. Among authors: biolcati g. Arch Dis Child. 2015 Jan;100(1):7. doi: 10.1136/archdischild-2014-307082. Epub 2014 Nov 12. Arch Dis Child. 2015. PMID: 25392202 No abstract available.

8

Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.

Radio FC, Majore S, Aurizi C, Sorge F, Biolcati G, Bernabini S, Giotti I, Torricelli F, Giannarelli D, De Bernardo C, Grammatico P. Radio FC, et al. Among authors: biolcati g. Blood Cells Mol Dis. 2015 Jun;55(1):71-5. doi: 10.1016/j.bcmd.2015.04.001. Epub 2015 Apr 16. Blood Cells Mol Dis. 2015. PMID: 25976471

9

Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy.

Martinez di Montemuros F, Di Pierro E, Biolcati G, Rocchi E, Bissolotti E, Tavazzi D, Fiorelli G, Cappellini MD. Martinez di Montemuros F, et al. Among authors: biolcati g. Blood Cells Mol Dis. 2001 Nov-Dec;27(6):961-70. doi: 10.1006/bcmd.2001.0466. Blood Cells Mol Dis. 2001. PMID: 11831862

10

Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?

D'Alessandro Gandolfo L, Griso D, Macri A, Biolcati G, Topi GC. D'Alessandro Gandolfo L, et al. Among authors: biolcati g. Dermatologica. 1989;178(4):206-8. doi: 10.1159/000248428. Dermatologica. 1989. PMID: 2767288

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