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Valentina Brancaleoni

Showing results (1-10 of 38) with videos related to

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Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: CPOX. Disease: coproporphyriaElena DiPierro, Valentina Brancaleoni, Maria Domenica Cappellini
British Journal of Haematology|March 13, 2016
Advances in understanding the pathogenesis of congenital erythropoietic porphyriaElena Di Pierro, Valentina Brancaleoni, Francesca Granata
Journal of Human Genetics|July 25, 2009
Multiplex ligation-dependent probe amplification: a novel approach for genetic diagnosis of PorphyriaElena Di Pierro, Valentina Brancaleoni, Valeria Besana, et al.
Mediterranean Journal of Hematology and Infectious Diseases|November 16, 2020
Activin Receptor-Ligand Trap for the Treatment of β-thalassemia: A Serendipitous DiscoveryValentina Brancaleoni, Isabella Nava, Paola Delbini, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Dipierro, S Ausenda, et al.
Blood Cells, Molecules & Diseases|September 27, 2016
The assessment of noncoding variant of PPOX gene in variegate porphyria reveals post-transcriptional role of the 5' untranslated exon 1Valeria Fiorentino, Valentina Brancaleoni, Francesca Granata, et al.
Human Genetics|October 21, 2010
Gene symbol: FECH. Disease: Porphyria, ErythropoieticValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|October 11, 2008
Gene symbol: FECH. Disease: Porphyria, erythropoieticValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|June 29, 2007
Gene symbol: URODValentina Brancaleoni, E Di Pierro, S Ausenda, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: CPOX. Disease: coproporphyriaElena DiPierro, Valentina Brancaleoni, Maria Domenica Cappellini
British Journal of Haematology|March 13, 2016
Advances in understanding the pathogenesis of congenital erythropoietic porphyriaElena Di Pierro, Valentina Brancaleoni, Francesca Granata
Journal of Human Genetics|July 25, 2009
Multiplex ligation-dependent probe amplification: a novel approach for genetic diagnosis of PorphyriaElena Di Pierro, Valentina Brancaleoni, Valeria Besana, et al.
Mediterranean Journal of Hematology and Infectious Diseases|November 16, 2020
Activin Receptor-Ligand Trap for the Treatment of β-thalassemia: A Serendipitous DiscoveryValentina Brancaleoni, Isabella Nava, Paola Delbini, et al.
Human Genetics|March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Dipierro, S Ausenda, et al.
Blood Cells, Molecules & Diseases|September 27, 2016
The assessment of noncoding variant of PPOX gene in variegate porphyria reveals post-transcriptional role of the 5' untranslated exon 1Valeria Fiorentino, Valentina Brancaleoni, Francesca Granata, et al.
Human Genetics|October 21, 2010
Gene symbol: FECH. Disease: Porphyria, ErythropoieticValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneousValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|October 11, 2008
Gene symbol: FECH. Disease: Porphyria, erythropoieticValentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics|June 29, 2007
Gene symbol: URODValentina Brancaleoni, E Di Pierro, S Ausenda, et al.
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