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Human Genetics
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April 15, 2011
Novel human pathological mutations. Gene symbol: CPOX. Disease: coproporphyria
Elena DiPierro, Valentina Brancaleoni, Maria Domenica Cappellini
British Journal of Haematology
|
March 13, 2016
Advances in understanding the pathogenesis of congenital erythropoietic porphyria
Elena 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 Porphyria
Elena 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 Discovery
Valentina Brancaleoni, Isabella Nava, Paola Delbini, et al.
Human Genetics
|
March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous
Valentina 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 1
Valeria Fiorentino, Valentina Brancaleoni, Francesca Granata, et al.
Human Genetics
|
October 21, 2010
Gene symbol: FECH. Disease: Porphyria, Erythropoietic
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
October 11, 2008
Gene symbol: FECH. Disease: Porphyria, erythropoietic
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
June 29, 2007
Gene symbol: UROD
Valentina Brancaleoni, E Di Pierro, S Ausenda, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Human Genetics
|
April 15, 2011
Novel human pathological mutations. Gene symbol: CPOX. Disease: coproporphyria
Elena DiPierro, Valentina Brancaleoni, Maria Domenica Cappellini
British Journal of Haematology
|
March 13, 2016
Advances in understanding the pathogenesis of congenital erythropoietic porphyria
Elena 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 Porphyria
Elena 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 Discovery
Valentina Brancaleoni, Isabella Nava, Paola Delbini, et al.
Human Genetics
|
March 20, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous
Valentina 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 1
Valeria Fiorentino, Valentina Brancaleoni, Francesca Granata, et al.
Human Genetics
|
October 21, 2010
Gene symbol: FECH. Disease: Porphyria, Erythropoietic
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
October 11, 2008
Gene symbol: FECH. Disease: Porphyria, erythropoietic
Valentina Brancaleoni, E Di Pierro, V Besana, et al.
Human Genetics
|
June 29, 2007
Gene symbol: UROD
Valentina Brancaleoni, E Di Pierro, S Ausenda, et al.
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of 4