| Titolo | Data di pubblicazione | Autori | Tipo | Abstract |
|---|
| IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA | 2019 | 112. Littera R; CHESSA, LUCHINO ; PERRA, ANDREA ; LAI, SARA ; SERRA, MANUELA ; Maddi R; LOI, VALENTINA ; RAGATZU, PAOLA ; CONGEDDU, ELENA ; ALBA, FRANCESCA ; FIGORILLI, FRANCESCO ; Manieli C; ONALI, SIMONA ; CASALE, MICHELE ; BARCA, LUCIA ; ORRU, SANDRO ; CARCASSI, CARLO | 1 Contributo su Rivista::1.5 Abstract in rivista | - |
| Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients | 2017 | Mitropoulos K; MERKOURI PAPADIMA, ELENI ; Xiromerisiou G; Balasopoulou A; Charalampidou K; Galani V; Zafeiri KV; Dardiotis E; Ralli S; Deretzi G; John A; Kydonopoulou K; Papadopoulou E; di Pardo A; Akcimen F; Loizedda A; Dobričić V; Novaković I; Kostić VS; Mizzi C; Peters BA; Basak N; ORRU, SANDRO ; Kiskinis E; Cooper DN; Gerou S; Drmanac R; Bartsakoulia M; Tsermpini EE; Hadjigeorgiou GM; Ali BR; Katsila T; Patrinos G.P. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients | 2017 | SANTORU, MARIA LAURA ; PIRAS, CRISTINA ; MURGIA, ANTONIO ; PALMAS, VANESSA ; CAMBONI, TANIA ; LIGGI, SONIA ; IBBA, IVAN ; Lai, Maria Antonia; ORRU, SANDRO ; Loizedda, Anna Lisa; GRIFFIN, JULIAN LEETHER; USAI, PAOLO ; CABONI, PIERLUIGI ; ATZORI, LUIGI ; MANZIN, ALDO | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia | 2017 | CAOCCI, GIOVANNI ; Greco, Marianna; Arras, Marcella; Cusano, Roberto; ORRU, SANDRO ; Martino, Bruno; Abruzzese, Elisabetta; Galimberti, Sara; Mulas, Olga; Trucas, Marcello; Littera, Roberto; Lai, Sara; CARCASSI, CARLO ; LA NASA, GIORGIO | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients | 2017 | PALMAS, VANESSA ; SANTORU, MARIA LAURA ; PIRAS, CRISTINA ; MURGIA, ANTONIO ; CAMBONI, TANIA ; LIGGI, SONIA ; IBBA, IVAN ; ORRU, SANDRO ; Loizedda, Anna Lisa; USAI, PAOLO ; CABONI, PIERLUIGI ; ATZORI, LUIGI ; MANZIN, ALDO | 4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno | - |
| KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation | 2017 | Littera, Roberto; Piredda, Gianbenedetto; Argiolas, Davide; Lai, Sara; Congeddu, Elena; Ragatzu, Paola; Melis, Maurizio; Carta, Elisabetta; Michittu, Maria Benigna; Valentini, Donatella; Cappai, Luisella; Porcella, Rita; Alba, Francesco; Serra, Maria; Loi, Valentina; Maddi, Roberta; ORRU, SANDRO ; LA NASA, GIORGIO ; CAOCCI, GIOVANNI ; Cusano, Roberto; Arras, Marcella; Frongia, Mauro; Pani, Antonello; CARCASSI, CARLO | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function. | 2016 | ORRU, SANDRO ; CONI, PAOLA ; FLORIS, ANDREA ; Littera, R; CARCASSI, CARLO ; SOGOS, VALERIA ; BRANCIA, CARLA | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis | 2016 | Leblond, Claire S; Gan Or, Ziv; Spiegelman, Dan; Laurent, Sandra B; Szuto, Anna; Hodgkinson, Alan; Dionne Laporte, Alexandre; Provencher, Pierre; de Carvalho, Mamede; ORRU, SANDRO ; Brunet, Denis; Bouchard, Jean Pierre; Awadalla, Philip; Dupré, Nicolas; Dion, Patrick A; Rouleau, Guy A. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics | 2016 | LA NASA, GIORGIO ; Vacca, Adriana; Littera, Roberto; Piras, Eugenia; ORRU, SANDRO ; Greco, Marianna; CARCASSI, CARLO ; CAOCCI, GIOVANNI | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY | 2016 | DELEDDA, ANDREA ; BOI, ALESSANDRO ; SCANO, SIMONA ; PISANU, SILVIA ; LOVISELLI, ANDREA ; PALMAS, VANESSA ; CAMBONI, TANIA ; ORRU, SANDRO ; Loi, E.; MANZIN, ALDO ; VELLUZZI, FERNANDA | 4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno | |
| VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies | 2016 | BRANCIA, CARLA ; NOLI, BARBARA ; Boido, Marina; Boi, Andrea; Puddu, Roberta; Borghero, Giuseppe; MARROSU, FRANCESCO ; Bongioanni, Paolo; ORRU, SANDRO ; MANCONI, BARBARA ; D'AMATO, FILOMENA ; MESSANA, IRENE ; Vincenzoni, Federica; Vercelli, Alessandro; FERRI, GIAN LUCA ; COCCO, CRISTINA | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis | 2016 | Littera, Roberto; CHESSA, LUCHINO ; ONALI, SIMONA ; FIGORILLI, FRANCESCO ; Lai, Sara; Secci, Luca; LA NASA, GIORGIO ; CAOCCI, GIOVANNI ; Arras, Marcella; Melis, Maurizio; Cappellini, Sara; Balestrieri, Cinzia; Serra, Giancarlo; Conti, Maria; Zolfino, Teresa; CASALE, MICHELE ; CASU, STEFANIA ; Pasetto, Maria Cristina; BARCA, LUCIA ; Salustro, Claudia; MATTA, LAURA ; SCIOSCIA, ROSETTA ; Zamboni, Fausto; FAA, GAVINO ; ORRU, SANDRO ; CARCASSI, CARLO | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male | 2015 | Papoulidis, Ioannis; Paspaliaris, Vassilis; Siomou, Elisavet; ORRU, SANDRO ; Murru, Roberta; Sifakis, Stavros; Nikolaidis, Petros; Garas, Antonios; Sotiriou, Sotirios; Thomaidis, Loretta; Manolakos, Emmanouil | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome | 2015 | Papadimitriou, D. T.; Manolakos, E.; Bothou, C.; Zoupanos, G.; Papoulidis, I.; ORRU, SANDRO ; Skarmoutsos, F.; Delides, A.; Bakoula, C.; Papadimitriou, A.; Urano, F. | 1 Contributo su Rivista::1.1 Articolo in rivista | - |
| Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases | 2015 | Papoulidis, Ioannis; Sotiriadis, Alexandros; Siomou, Elisavet; Papageorgiou, Elena; Eleftheriades, Makarios; Papadopoulos, Vasilios; Oikonomidou, Eirini; ORRU, SANDRO ; Manolakos, Emmanouil; Athanasiadis, Apostolos | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia | 2015 | Daoud, Hussein; Papadima, Eleni Merkouri; Ouled Amar Bencheikh, Bouchra; Katsila, Theodora; Dionne Laporte, Alexandre; Spiegelman, Dan; Dion, Patrick A.; Patrinos, George P.; ORRU, SANDRO ; Rouleau, Guy A. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature | 2014 | Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; ORRU, SANDRO ; Ziegler M; Liehr T; Manolakos E; Papoulidis I. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report | 2014 | Papoulidis I; Oikonomidou E; ORRU, SANDRO ; Siomou E; Kontodiou M; Eleftheriades M; Bacoulas V; Cigudosa JC; Suela J; Thomaidis L; Manolakos E. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
| ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION | 2014 | SOGOS, VALERIA ; BRANCIA, CARLA ; Coni P; Floris A; Bellini I; ORRU, SANDRO | 4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno | - |
| A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics | 2014 | Lagou M; Papoulidis I; ORRU, SANDRO ; Papadopoulos V; Daskalakis G; Kontodiou M; Anastasakis E; Petersen MB; Kitsos G; Thomaidis L; Manolakos E. | 1 Contributo su Rivista::1.1 Articolo in rivista | |
