Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Current Opinion in Pediatrics|July 14, 2012
Wolfram syndrome 1 and Wolfram syndrome 2Luciana Rigoli, Chiara Di Bella
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|September 15, 2019
Iron overload and malignancies in patients with haemoglobinopathies: A single center experienceLuciana Rigoli, Annamaria Petrungaro, Chiara Di Bella, et al.
Pediatric Research|May 19, 2018
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative diseaseLuciana Rigoli, Placido Bramanti, Chiara Di Bella, et al.
Pediatric Research|September 2, 2018
Correction: Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative diseaseLuciana Rigoli, Placido Bramanti, Chiara Di Bella, et al.
Annals of Hematology|September 5, 2006
Identification of alpha-thalassemia mutations in subjects from Eastern Sicily (Italy) with abnormal hematological indices and normal Hb A2Chiara Di Bella, Carmelo Salpietro, Mariangela La Rosa, et al.
Gene|October 30, 2012
Identification of one novel causative mutation in exon 4 of WFS1 gene in two Italian siblings with classical DIDMOAD syndrome phenotypeLuciana Rigoli, Fortunato Lombardo, Giuseppina Salzano, et al.
Pediatric Research|October 8, 2004
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathiesLuciana Rigoli, Roberto Chimenz, Chiara di Bella, et al.
Annals of Human Genetics|June 23, 2015
Prevalence of Deafness-Associated Connexin-26 (GJB2) and Connexin-30 (GJB6) Pathogenic Alleles in a Large Patient Cohort from Eastern SicilyMaria Amorini, Petronilla Romeo, Rocco Bruno, et al.
Allergy and Asthma Proceedings|January 19, 2008
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian childrenLuciana Rigoli, Chiara Di Bella, Vincenzo Procopio, et al.
Human Mutation|May 20, 2003
Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assayAlessia Colosimo, Valentina Guida, Luciana Rigoli, et al.
Pageof 6