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E Di Pierro

Showing results (31-40 of 39) with videos related to

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Blood Cells, Molecules & Diseases|February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in ItalyF Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegateSabrina Ausenda, V Moriondo, S Marchini, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 18, 2003
Molecular characterization of porphyrias in Italy: a diagnostic flow-chartF Martinez di Montemuros, E Di Pierro, E Patti, et al.
The British Journal of Dermatology|March 21, 2012
A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia traitJ E Maakaron, O Abdel Malak, S Itani, et al.
Annals of Hematology|July 22, 2017
Transcranial color Doppler in stroke-free adult patients with sickle cell diseaseG Graziadei, F M Casoni, F Annoni, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Clinical, biochemical and genetic characteristics of Variegate Porphyria in ItalyE Di Pierro, P Ventura, V Brancaleoni, et al.
Clinical Genetics|January 24, 2015
X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyriaV Brancaleoni, M Balwani, F Granata, et al.
European Review for Medical and Pharmacological Sciences|May 6, 2024
Recovery of chronic motor neuropathy due to acute intermittent porphyria after givosiran treatment in a young boy: a case reportM Mazzoli, A Ricci, A E Vaudano, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Blood Cells, Molecules & Diseases|February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in ItalyF Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegateSabrina Ausenda, V Moriondo, S Marchini, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 18, 2003
Molecular characterization of porphyrias in Italy: a diagnostic flow-chartF Martinez di Montemuros, E Di Pierro, E Patti, et al.
The British Journal of Dermatology|March 21, 2012
A puzzling mutation in congenital erythropoietic porphyria and an association with β-thalassaemia traitJ E Maakaron, O Abdel Malak, S Itani, et al.
Annals of Hematology|July 22, 2017
Transcranial color Doppler in stroke-free adult patients with sickle cell diseaseG Graziadei, F M Casoni, F Annoni, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Clinical, biochemical and genetic characteristics of Variegate Porphyria in ItalyE Di Pierro, P Ventura, V Brancaleoni, et al.
Clinical Genetics|January 24, 2015
X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyriaV Brancaleoni, M Balwani, F Granata, et al.
European Review for Medical and Pharmacological Sciences|May 6, 2024
Recovery of chronic motor neuropathy due to acute intermittent porphyria after givosiran treatment in a young boy: a case reportM Mazzoli, A Ricci, A E Vaudano, et al.
Pageof 4