ROSSINO, ROSSANO

ROSSINO, ROSSANO  

DIPARTIMENTO DI SCIENZE MEDICHE E SANITA' PUBBLICA  

Mostra records
Risultati 1 - 20 di 33 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autore(i) Rivista Editore
Peripheral blood mononuclear cells reactivity in recent-onset type I diabetes patients is directed against the leader peptide of preproinsulin, GAD65271-285 and GAD65431-450 1-gen-2023 Jores, Rita D; Baldera, Davide; Schirru, Enrico; Muntoni, Sandro; Rossino, Rossano; Manchinu, Maria F; Marongiu, Maria F; Caria, Cristian A; Ripoli, Carlo; Ricciardi, Maria R; Cucca, Francesco; Congia, Mauro FRONTIERS IN IMMUNOLOGY -
Antibodies targeting the European lobster (Palinurus elephas) vitellogenin developed by mRNA isolation and in-silico-designed antigenic peptides 1-gen-2022 Cannea, Faustina B; Follesa, Cristina; Porcu, Cristina; Rossino, Rossano; Olianas, Alessandra; Rescigno, Antonio; Padiglia, Alessandra BIOLOGY OPEN -
Celiac Disease and HLA Molecular Typing 1-gen-2022 Cannea, FAUSTINA BARBARA; Rossino, Rossano; Padiglia, Alessandra BIOMEDICAL JOURNAL OF SCIENTIFIC & TECHNICAL RESEARCH -
Toward the renal vesicle: Ultrastructural investigation of the cap mesenchyme splitting process in the developing kidney 1-gen-2022 Piras, M.; Gerosa, C.; Congiu, T.; Cau, F.; Fanni, D.; Pichiri, G.; Coni, P.; Lachowicz, J. I.; Schirru, E.; Congia, M.; Rossino, R.; Muntoni, S.; Jaremko, M.; Piludu, M. JOURNAL OF PUBLIC HEALTH RESEARCH -
Low-Risk Human Leukocyte Antigen Genes and Mild Villous Atrophy Typify Celiac Disease With Immunoglobulin A Deficiency 1-gen-2021 Schirru, E.; Jores, R. D.; Rossino, R.; Corpino, M.; Cucca, F.; Congia, M. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION -
Cryptic Chromosome rearrangements detected by BAC Genome Array-CGH 1-gen-2015 Cabras, V; Montaldo, Caterina; Rossino, Rossano; Caria, Paola; Nucaro, Al CHROMOSOME RESEARCH -
Anti-actin IgA antibodies identify celiac disease patients with a Marsh 3 intestinal damage among subjects with moderate anti-TG2 levels 1-gen-2013 Schirru, E; Danjou, Fabrice; Cicotto, L; Rossino, Rossano; Macis, M. D.; Lampis, R; Jores, R. D.; Congia, M. BIOMED RESEARCH INTERNATIONAL -
Utility of Anti-actin Iga Antibody in Combination with the New ESPGHAN Guidelines for Coeliac Disease Diagnosis 1-gen-2013 Schirru, Enrico; Danjou, Fabrice; Cicotto, Lucia; Musu Maria, Paola; Frau, Fulvia; Virgiliis Stefano, De; Rossino, Rossano; Macis Maria, Doloretta; Lampis, Rosanna; Jores Rita, Désirée; Congia, Mauro JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY RESEARCH -
High frequency of low-risk human leukocyte antigen class II genotypes in latent celiac disease 1-gen-2011 Schirru, E; Jores, Rd; Cicotto, L; Frau, F; De Virgiliis, S; Rossino, Rossano; Macis, Md; Lampis, R; Congia, M. HUMAN IMMUNOLOGY -
Methylenetetrahydrofolate reductase C677T gene polymorphism and homocysteine levels in the Sardinian population 1-gen-2011 Muntoni, Sa; Leoni, Vp; Atzori, L; Rossino, R; Muntoni, Se GIORNALE ITALIANO DELL'ARTERIOSCLEROSI Edizioni internazionali EDMES s.r.l.
Ring chromosome 14 mosaicism: an unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH. 1-gen-2010 Nucaro, Al; Falchi, M; Pisano, T; Rossino, Rossano; Boscarelli, F; Stoico, G; Milia, A; Montaldo, C; Cianchetti, C; Pruna, D. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A -
The impact of NOD2/CARD15 SNPs on the severe gastrointestinal GVHD following allogeneic Stem Cell Transplantation in Sardinia population 1-gen-2010 OROFINO M., G; Diana, D; Rossino, Rossano; ADDARI M., C; Cossu, F; Piroddi, A; Rizzo, F; Congia, M; Vacca, A; LA NASA, Giorgio; Badiali, M. BONE MARROW TRANSPLANTATION -
A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosis 1-gen-2008 Nucaro, A; Crisponi, G; Minafra, L; Rossino, Rossano; Cianchetti, C. GENETIC COUNSELING -
Familian traslocation t(3;10)(p26.3;p12.31)leading to trisomy 10p12.31..pter and monosomy 3p26.3..pter in seven members 1-gen-2008 Nucaro, Al1; Meloni, M; Pisano, T; Melis, P; Rossi, E; Rossino, R; Corona, S; Loi, M; Achena, F; Zuffardi, Orsetta; Cianchetti, C. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A -
Turner syndrome mosaicism: an unusual case with a de novo large dicentric marker chromosome: mos 45,X/46,X, ter rea(X;X)(p22.3;p22.3) 1-gen-2008 Nucaro, Al; Melis, P; Casini, Mr; Rossino, Rossano; Cau, Milena; Melis, Ma; Loche, S. JOURNAL OF APPLIED GENETICS -
Decline of lactase activity and c/t-13910 variant in Sardinian childhood 1-gen-2007 Schirru, E; Corona, V; USAI SATTA, P; Scarpa, M; Cucca, F; DE VIRGILIIS, S; Rossino, Rossano; Frau, F; Macis, Md; Jores, Rd; Congia, M. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION -
GENETIC TESTING IMPROVES THE DIAGNOSIS OF ADULT TYPE HYPOLACTASIA IN THE MEDITERRANEAN POPULATION OF SARDINIA 1-gen-2007 Schirru, E; Corona, V; USAI SATTA, P; Scarpa, M; Oppia, F; Loriga, F; Cucca, F; DE VIRGILIIS, S; Rossino, Rossano; DOLORETTA MACIS, M; Jores, Rd; Congia, M. EUROPEAN JOURNAL OF CLINICAL NUTRITION -
Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia 1-gen-2006 Rossino, Rossano; Vincis, C; Alves, S; Prata, Mj; Macis, Md; Nucaro, Al; Schirru, E; Congia, M. JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS -
Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes 1-gen-2006 Nucaro, Al; Rossino, Rossano; Pruna, D; Rassu, S; Cianchetti, C; Cao, A; Moi, Paolo PRENATAL DIAGNOSIS -
Prenatal diagnosis of a double trisomy 48, XXY, +13: Klinefelter and Patau syndromes 1-gen-2005 Rossino, Rossano; Nucaro, AMERICAN JOURNAL OF MEDICAL GENETICS. PART A -