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American Journal of Medical Genetics. Part A|September 19, 2009
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtiaCarmelo Damiano Salpietro, Silvana Briuglia, Maria Concetta Cutrupi, et al.
Ultrastructural Pathology|January 9, 2015
Eosinophil-Specific Granules in Tumor Cell Cytoplasm: Unusual Ultrastructural Findings in a Case of Diffuse-Type Gastric CarcinomaRosario Alberto Caruso, Giovanni Branca, Francesco Fedele, et al.
European Journal of Haematology|September 10, 2014
Endocrinopathies, metabolic disorders, and iron overload in major and intermedia thalassemia: serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessmentValeria Chirico, Luciana Rigoli, Antonio Lacquaniti, 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.
Ultrastructural Pathology|October 30, 2008
Microvascular changes in human gastric carcinomas with coagulative necrosis: an ultrastructural studyRosario Alberto Caruso, Francesco Fedele, Giuseppe Finocchiaro, et al.
Rare Tumors|July 27, 2013
Apoptotic-like tumor cells and apoptotic neutrophils in mitochondrion-rich gastric adenocarcinomas: a comparative study with light and electron microscopy between these two forms of cell deathRosario A Caruso, Francesco Fedele, Luciana Rigoli, 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.
Microorganisms|March 1, 2020
Evolutionarily-Related Helicobacter pylori Genotypes and Gastric Intraepithelial Neoplasia in a High-Risk Area of Northern ItalySonia Toracchio, Rosario Alberto Caruso, Silvia Perconti, 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.
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