Laboratory diagnosis of thalassemia
Brancaleoni, V., Di Pierro, E., Motta, I., Cappellini, M. D.
Published in International journal of laboratory hematology (01.05.2016)
Published in International journal of laboratory hematology (01.05.2016)
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X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyria
Brancaleoni, V., Balwani, M., Granata, F., Graziadei, G., Missineo, P., Fiorentino, V., Fustinoni, S., Cappellini, M.D., Naik, H., Desnick, R.J., Di Pierro, E.
Published in Clinical genetics (01.01.2016)
Published in Clinical genetics (01.01.2016)
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A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia trait
Maakaron, J.E., Abdel Malak, O., Itani, S., Cappellini, M.D., Di Pierro, E., Brancaleoni, V., Granata, F., Taher, A.T.
Published in British journal of dermatology (1951) (01.09.2012)
Published in British journal of dermatology (1951) (01.09.2012)
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Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittent
Di Pierro, Elena, Brancaleoni, V, Stanzial, F, Benedicenti, F, Castellan, C, Cappellini, M D
Published in Human genetics (01.08.2009)
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Published in Human genetics (01.08.2009)
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Novel human pathological mutations. Gene symbol: CPOX. Disease: Coproporphyria
Ausenda, Sabrina, Di Pierro, E, Brancaleoni, V, Tavazzi, D, Cappellini, M D
Published in Human genetics (01.08.2009)
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Published in Human genetics (01.08.2009)
Journal Article
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent
Besana, Valeria, Di Pierro, E, Brancaleoni, V, Sabrina, A, Fiocchi, M, Cappellini, M D
Published in Human genetics (01.04.2009)
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Published in Human genetics (01.04.2009)
Journal Article
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate
Ausenda, Sabrina, Moriondo, V, Marchini, S, Besana, V, Di Pierro, E, Brancaleoni, V, Ventura, P, Rocchi, E, Cappellini, M D
Published in Human genetics (01.04.2009)
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Published in Human genetics (01.04.2009)
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Gene symbol: PPOX. Disease: Porphyria, variegate
Ausenda, Sabrina, Di Pierro, E, Besana, V, Brancaleoni, V, Cappellini, M D
Published in Human genetics (01.02.2008)
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Published in Human genetics (01.02.2008)
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Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy
Di Pierro, E, Ventura, P, Brancaleoni, V, Moriondo, V, Marchini, S, Tavazzi, D, Nascimbeni, F, Ferrari, M C, Rocchi, E, Cappellini, M D
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01.07.2009)
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01.07.2009)
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Journal Article
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate
Ausenda, S, Di Pierro, E, Brancaleoni, V, Besana, V, Cappellini, M D
Published in Human genetics (01.11.2007)
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Published in Human genetics (01.11.2007)
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Novel human pathological mutations. Gene symbol: FECH. Disease: porphyria, erythropoietic
Brancaleoni, V, Di Pierro, E, Besana, V, Ausenda, S, Drury, S, Cappellini, M D
Published in Human genetics (01.06.2007)
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Published in Human genetics (01.06.2007)
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Gene symbol: HMBS. Disease: porphyria, acute intermittent
Di Pierro, E, Besana, V, Moriondo, V, Brancaleoni, V, Cappellini, M D
Published in Human genetics (01.04.2006)
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Published in Human genetics (01.04.2006)
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Gene symbol: CPOX
Ausenda, Sabrina, Di Pierro, E, Besana, V, Brancaleoni, V, Cappellini, M D
Published in Human genetics (01.04.2007)
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Published in Human genetics (01.04.2007)
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Gene symbol: HMBS
Besana, V, Di Pierro, E, Brancaleoni, V, Ausenda, S, Cappellini, M D
Published in Human genetics (01.04.2007)
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Published in Human genetics (01.04.2007)
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Gene symbol: HMBS. Disease: porphyria, acute intermittent
Di Pierro, E, Besana, V, Ausenda, S, Brancaleoni, V, Cappellini, M D
Published in Human genetics (01.04.2006)
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Published in Human genetics (01.04.2006)
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Gene symbol: HMBS. Disease: porphyria, acute intermittent
Di Pierro, E, Besana, V, Brancaleoni, V, Moriondo, V, Cappellini, M D
Published in Human genetics (01.04.2006)
Published in Human genetics (01.04.2006)
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Journal Article
Gene symbol: FECH. Disease: Porphyria, erythropoietic. Accession #Hg0501
Di Pierro, E, Brancaleoni, V, Moriondo, V, Besana, V, Cappellini, M D
Published in Human genetics (01.02.2006)
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Published in Human genetics (01.02.2006)
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Epidemiology of porphyrias in Italy: rare complex diseases with liver involvement- data from the registry of Gruppo Italiano Porfiria (GrIP)
Ventura, P., Cappellini, M., Macrì, A., Guida, C., Nicolli, A., Rossi, M., Di Pierro, E., Brancaleoni, V., Granata, F., Fiorentino, V., Fustinoni, S., Sala, R., Calzavara-Pinton, P.G., Trevisan, A., Marchini, S., Cuoghi, C., Marcacci, M., Pietrangelo, A., Sorge, F., Aurizi, C., Savino, M.G.
Published in Digestive and liver disease (01.02.2019)
Published in Digestive and liver disease (01.02.2019)
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