Sfoglia per Autore
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics
2016-01-01 LA NASA, Giorgio; Vacca, Adriana; Littera, Roberto; Piras, Eugenia; Orru, Sandro; Greco, Marianna; Carcassi, Carlo; Caocci, Giovanni
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY
2016-01-01 Deledda, Andrea; Boi, Alessandro; Scano, Simona; Pisanu, Silvia; Loviselli, Andrea; Palmas, Vanessa; Camboni, Tania; Orru, Sandro; Loi, E.; Manzin, Aldo; Velluzzi, Fernanda
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis
2016-01-01 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
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies
2016-01-01 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
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male
2015-01-01 Papoulidis, Ioannis; Paspaliaris, Vassilis; Siomou, Elisavet; Orru, Sandro; Murru, Roberta; Sifakis, Stavros; Nikolaidis, Petros; Garas, Antonios; Sotiriou, Sotirios; Thomaidis, Loretta; Manolakos, Emmanouil
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases
2015-01-01 Papoulidis, Ioannis; Sotiriadis, Alexandros; Siomou, Elisavet; Papageorgiou, Elena; Eleftheriades, Makarios; Papadopoulos, Vasilios; Oikonomidou, Eirini; Orru, Sandro; Manolakos, Emmanouil; Athanasiadis, Apostolos
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome
2015-01-01 Papadimitriou, D. T.; Manolakos, E.; Bothou, C.; Zoupanos, G.; Papoulidis, I.; Orru, Sandro; Skarmoutsos, F.; Delides, A.; Bakoula, C.; Papadimitriou, A.; Urano, F.
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia
2015-01-01 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.
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION
2014-01-01 Sogos, Valeria; Brancia, Carla; Coni, P; Floris, A; Bellini, I; Orru, Sandro
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature
2014-01-01 Sifakis, S; Eleftheriades, M; Kappou, D; Murru, R; Konstantinidou, A; Orru, Sandro; Ziegler, M; Liehr, T; Manolakos, E; Papoulidis, I.
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report
2014-01-01 Papoulidis, I; Oikonomidou, E; Orru, Sandro; Siomou, E; Kontodiou, M; Eleftheriades, M; Bacoulas, V; Cigudosa, Jc; Suela, J; Thomaidis, L; Manolakos, E.
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics
2014-01-01 Lagou, M; Papoulidis, I; Orru, Sandro; Papadopoulos, V; Daskalakis, G; Kontodiou, M; Anastasakis, E; Petersen, Mb; Kitsos, G; Thomaidis, L; Manolakos, E.
Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients.
2013-01-01 Coni, P; Brancia, Carla; Floris, A; Bellini, I; Orru, Sandro; Sogos, Valeria
Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome
2013-01-01 Caocci, Giovanni; Baccoli, Roberto; Littera, ; Orru, Sandro; Carcassi, Carlo; LA NASA, Giorgio
Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes
2013-01-01 Littera, R; Piredda, G; Pani, A; Frongia, M; Onano, B; Michittu M., B; Murgia M., G; Lai, S; Alba, F; Valentini M., D; Loi, V; Caocci, Giovanni; Orru, Sandro; LA NASA, Giorgio; Carcassi, Carlo
Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia
2013-01-01 Caocci, Giovanni; LA NASA, Giorgio; Littera, R; Atzeni, S; Vacca, A; Mulas, O; Langiu, M; Greco, M; Orru, Sandro; Orrù, N; Usai, M; Floris, A; Carcassi, Carlo
De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia
2013-01-01 Papoulidis, I; Vetro, A; Kefalas, K; Orru, Sandro; Thomaidis, L; Iliodromiti, Z; Zuffardi, O; Manolakos, E.
Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients
2013-01-01 Brancia, Carla; Coni, Paola; Floris, A; Bellini, I; Orru, Sandro; Sogos, Valeria
Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma
2013-01-01 Littera, R; Zamboni, F; Tondolo, V; Fantola, G; Chessa, Luchino; Orrù, N; Sanna, M; Valentini, D; Cappai, L; Mulargia, M; Caocci, Giovanni; Arras, M; Floris, Andrea; Orru, Sandro; LA NASA, Giorgio; Carcassi, Carlo
Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients
2013-01-01 LA NASA, Giorgio; Caocci, Giovanni; Littera, R; Atzeni, S; Vacca, A; Mulas, O; Langiu, M; Greco, M; Orru, Sandro; Orrù, N; Floris, Andrea; Carcassi, Carlo
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics | 1-gen-2016 | LA NASA, Giorgio; Vacca, Adriana; Littera, Roberto; Piras, Eugenia; Orru, Sandro; Greco, Marianna; Carcassi, Carlo; Caocci, Giovanni | MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES | - |
| GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY | 1-gen-2016 | Deledda, Andrea; Boi, Alessandro; Scano, Simona; Pisanu, Silvia; Loviselli, Andrea; Palmas, Vanessa; Camboni, Tania; Orru, Sandro; Loi, E.; Manzin, Aldo; Velluzzi, Fernanda | EATING AND WEIGHT DISORDERS | Springer International Publishing Switzerland |
| Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis | 1-gen-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 | PLOS ONE | - |
| VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies | 1-gen-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 | PLOS ONE | - |
| Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male | 1-gen-2015 | Papoulidis, Ioannis; Paspaliaris, Vassilis; Siomou, Elisavet; Orru, Sandro; Murru, Roberta; Sifakis, Stavros; Nikolaidis, Petros; Garas, Antonios; Sotiriou, Sotirios; Thomaidis, Loretta; Manolakos, Emmanouil | MOLECULAR CYTOGENETICS | - |
| Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases | 1-gen-2015 | Papoulidis, Ioannis; Sotiriadis, Alexandros; Siomou, Elisavet; Papageorgiou, Elena; Eleftheriades, Makarios; Papadopoulos, Vasilios; Oikonomidou, Eirini; Orru, Sandro; Manolakos, Emmanouil; Athanasiadis, Apostolos | PRENATAL DIAGNOSIS | - |
| Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome | 1-gen-2015 | Papadimitriou, D. T.; Manolakos, E.; Bothou, C.; Zoupanos, G.; Papoulidis, I.; Orru, Sandro; Skarmoutsos, F.; Delides, A.; Bakoula, C.; Papadimitriou, A.; Urano, F. | DIABETES & METABOLISM | - |
| Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia | 1-gen-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. | EUROPEAN JOURNAL OF MEDICAL GENETICS | - |
| ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION | 1-gen-2014 | Sogos, Valeria; Brancia, Carla; Coni, P; Floris, A; Bellini, I; Orru, Sandro | - | - |
| Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature | 1-gen-2014 | Sifakis, S; Eleftheriades, M; Kappou, D; Murru, R; Konstantinidou, A; Orru, Sandro; Ziegler, M; Liehr, T; Manolakos, E; Papoulidis, I. | BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY | - |
| Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report | 1-gen-2014 | Papoulidis, I; Oikonomidou, E; Orru, Sandro; Siomou, E; Kontodiou, M; Eleftheriades, M; Bacoulas, V; Cigudosa, Jc; Suela, J; Thomaidis, L; Manolakos, E. | MOLECULAR MEDICINE REPORTS | - |
| A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics | 1-gen-2014 | Lagou, M; Papoulidis, I; Orru, Sandro; Papadopoulos, V; Daskalakis, G; Kontodiou, M; Anastasakis, E; Petersen, Mb; Kitsos, G; Thomaidis, L; Manolakos, E. | MOLECULAR CYTOGENETICS | - |
| Stress granule assembly in cultured fibroblast from TDP-43 mutant ALS patients. | 1-gen-2013 | Coni, P; Brancia, Carla; Floris, A; Bellini, I; Orru, Sandro; Sogos, Valeria | - | - |
| Comparison Between an Artificial Neural Network and Logistic Regression in Predicting Long Term Kidney Transplantation Outcome | 1-gen-2013 | Caocci, Giovanni; Baccoli, Roberto; Littera, ; Orru, Sandro; Carcassi, Carlo; LA NASA, Giorgio | - | InTech (Open Access Publisher) |
| Role of human leukocyte antigen-G 14-base pair polymorphism in kidney transplantation outcomes | 1-gen-2013 | Littera, R; Piredda, G; Pani, A; Frongia, M; Onano, B; Michittu M., B; Murgia M., G; Lai, S; Alba, F; Valentini M., D; Loi, V; Caocci, Giovanni; Orru, Sandro; LA NASA, Giorgio; Carcassi, Carlo | JN. JOURNAL OF NEPHROLOGY | - |
| Kir haplotype aa is a possible predictive marker of complete molecular response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia | 1-gen-2013 | Caocci, Giovanni; LA NASA, Giorgio; Littera, R; Atzeni, S; Vacca, A; Mulas, O; Langiu, M; Greco, M; Orru, Sandro; Orrù, N; Usai, M; Floris, A; Carcassi, Carlo | HAEMATOLOGICA | - |
| De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by oligospermia | 1-gen-2013 | Papoulidis, I; Vetro, A; Kefalas, K; Orru, Sandro; Thomaidis, L; Iliodromiti, Z; Zuffardi, O; Manolakos, E. | MOLECULAR SYNDROMOLOGY | - |
| Stress granules induced by oxidative stress in cultured fibroblast from TDP-43 mutant ALS patients | 1-gen-2013 | Brancia, Carla; Coni, Paola; Floris, A; Bellini, I; Orru, Sandro; Sogos, Valeria | ITALIAN JOURNAL OF ANATOMY AND EMBRYOLOGY | - |
| Absence of activating killer immunoglobulin-like receptor genes combined with hepatitis C viral genotype is predictive of hepatocellular carcinoma | 1-gen-2013 | Littera, R; Zamboni, F; Tondolo, V; Fantola, G; Chessa, Luchino; Orrù, N; Sanna, M; Valentini, D; Cappai, L; Mulargia, M; Caocci, Giovanni; Arras, M; Floris, Andrea; Orru, Sandro; LA NASA, Giorgio; Carcassi, Carlo | HUMAN IMMUNOLOGY | - |
| Homozygosity for killer immunoglobin-like receptor haplotype A predicts complete molecular response to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients | 1-gen-2013 | LA NASA, Giorgio; Caocci, Giovanni; Littera, R; Atzeni, S; Vacca, A; Mulas, O; Langiu, M; Greco, M; Orru, Sandro; Orrù, N; Floris, Andrea; Carcassi, Carlo | EXPERIMENTAL HEMATOLOGY | - |
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