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European Journal of Haematology|September 25, 2014
Congenital erythropoietic porphyria linked to GATA1-R216W mutation: challenges for diagnosisElena Di Pierro, Roberta Russo, Zeynep Karakas, et al.Photodermatology, Photoimmunology & Photomedicine|August 22, 2021
Ultraviolet A phototest positivity is associated with higher free erythrocyte protoporphyrin IX concentration and lower transferrin saturation values in erythropoietic protoporphyriaGiovanni Genovese, Carlo Alberto Maronese, Chiara Moltrasio, et al.Diagnostics (Basel, Switzerland)|December 24, 2021
Mechanisms of Neuronal Damage in Acute Hepatic PorphyriasAndrea Ricci, Elena Di Pierro, Matteo Marcacci, et al.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.Diagnostics (Basel, Switzerland)|May 28, 2022
Psychological Aspect and Quality of Life in Porphyrias: A ReviewGranata Francesca, Annamaria Nicolli, Alessia Colaiocco, et al.Journal of Clinical Medicine|February 26, 2025
Are Mitochondria a Potential Target for Treating β-Thalassemia?Elena Di Pierro, Valeria Di Stefano, Margherita Migone De Amicis, et al.Internal and Emergency Medicine|September 25, 2010
Porphyrias at a glance: diagnosis and treatmentMaria Domenica Cappellini, Valentina Brancaleoni, Giovanna Graziadei, et al.Clinical Chemistry and Laboratory Medicine|December 6, 2008
A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyriaChumei Li, Elena Di Pierro, Valentina Brancaleoni, et al.Blood Cells, Molecules & Diseases|September 25, 2007
A 10376 bp deletion of FECH gene responsible for erythropoietic protoporphyriaElena Di Pierro, Valentina Brancaleoni, Valeria Besana, et al.Experimental Hematology|April 27, 2005
A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyriaElena Di Pierro, Maria Domenica Cappellini, Renata Mazzucchelli, et al.Pageof 17