IL PORTALE per la RICERCA dei DIPARTIMENTI

G. Merlini, G. Palladini (2013) "A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis."

O. Zuffardi (2013) "A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasia."

Galliano M, Minchiotti L. (2013) "A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia."

Priori SG. (2013) "Abnormal Propagation of Calcium Waves and Ultrastructural Remodeling in Recessive Catecholaminergic Polymorphic Ventricular Tachycardia."

Massimiliano Gnecchi (2013) "Allogeneic Lethally Irradiated Cord Blood Mononuclear Cells in No-Option Critical Limb Ischemia: A “Box of Rain”"

Luisetti M, Ferrarotti I (2013) "Alpha1-antitrypsin deficiency - diagnostic testing and disease awareness in Germany and Italy."

Forlino A, Rossi A (2013) "Alteration of proteoglycan sulfation affects bone growth and remodeling."

Priori SG (2013) "Are hospitalized or ambulatory patients with heart failure treated in accordance with European Society of Cardiology guidelines? Evidence from 12,440 patients of the ESC Heart Failure Long-Term Registry"

A. Corsico, M. Luisetti (2013) "Assessment and management of pulmonary alveolar proteinosis in a reference center."

Luisetti M. (2013) "Augmentation therapy for alpha-1 antitrypsin deficiency: towards a personalised approach."

Priori SG. (2013) "CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia."

Crotti L. (2013) "Calmodulin mutations associated with recurrent cardiac arrest in infants."

I. Ferrarotti, M. Luisetti (2013) "Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels."

Arcaini L (2013) "Central nervous system involvement in mantle cell lymphoma: clinical features, prognostic factors and outcomes from the European Mantle Cell Lymphoma Network."

Gioia R, Forlino A (2013) "Characterization of stress response in human retinal epithelial cells."

Malcovati L, Cazzola M (2013) "Clinical and biological implications of driver mutations in myelodysplastic syndromes"

I. Ferrarotti, M. Luisetti (2013) "Clinical phenotypes of Italian and Spanish patients with a1-antitrypsin deficiency."

Visai L (2013) "Combined effects of Ag nanoparticles and oxygen plasma treatment on PLGA morphological, chemical, and antibacterial properties."

Crotti L., Torchio M. (2013) "Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death."

Malcovati L, Cazzola M (2013) "Complex Patterns of Chromosome 11 Aberrations in Myeloid Malignancies Target CBL, MLL, DDB1 and LMO2."

Minchiotti L, Galliano M (2013) "Congenital analbuminaemia: molecular defects and biochemical and clinical aspects."

Giuseppe D'Antona, Roberto Bottinelli (2013) "Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs"

O. Zuffardi (2013) "De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia."

Priori SG (2013) "Decreased RyR2 refractoriness determines myocardial synchronization of aberrant Ca2+ release in a genetic model of arrhythmia"

Malcovati L, Cazzola M (2013) "Development and validation of a prognostic scoring system for patients with chronic myelomonocytic leukemia"

Malcovati L, Cazzola M (2013) "Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet"

Gruppi C, Balduini A (2013) "Discoidin Domain Receptor 1 is a novel modulator of megakaryocyte-collagen interactions"

P. Patrizia Mangione (2013) "Distribution and determinants of circulating complement factor H concentration determined by a high-throughput immunonephelometric assay"

Priori S (2013) "ESC Core Curriculum for the General Cardiologist (2013)."

Arcaini L (2013) "ESMO Consensus conferences: guidelines on malignant lymphoma. part 2: marginal zone lymphoma, mantle cell lymphoma, peripheral T-cell lymphoma."

Bernasconi P, Passamonti F, Cazzola M. (2013) "Efficacy of ruxolitinib in chronic eosinophilic leukemia associated with a PCM1-JAK2 fusion gene."

Paulli M (2013) "Epstein-Barr virus infection and altered control of apoptotic pathways in posttransplant lymphoproliferative disorders."

S. G. Priori (2013) "Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes"

Priori SG (2013) "Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes."

Ricci V. (2013) "Expression and function of angiopoietins and their receptors in human basophils and mast cells."

Torchio M., Crotti L. (2013) "FGF12 is a candidate Brugada syndrome locus."

Danesino C (2013) "Familial adult-onset Pompe disease associated with unusual clinical and histological features."

Danesino C (2013) "Grade of pulmonary right-to-left shunt on contrast echocardiography and cerebral complications: a striking association."

Carla Olivieri (2013) "HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis"

Silvia G. Priori (2013) "HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes"

Francesco Passamonti (2013) "Health-related quality of life and symptoms in patients with myelofibrosis treated with ruxolitinibversusbest available therapy"

Arcaini L (2013) "Hepatitis C-associated B-cell non-Hodgkin lymphomas. Epidemiology, molecular signature and clinical management."

Minchiotti L, Galliano M (2013) "Human serum albumin isoforms: genetic and molecular aspects and functional consequences."

Crotti L. (2013) "Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome."

Cazzola M, Malcovati L (2013) "Identification of gene expression-based prognostic markers in the hematopoietic stem cells of patients with myelodysplastic syndromes"

Malcovati L, Cazzola M (2013) "Inappropriately low hepcidin levels in patients with myelodysplastic syndrome carrying a somatic mutation of SF3B1"

Priori SG (2013) "Induced pluripotent stem cell-derived cardiomyocytes in studies of inherited arrhythmias."

Di Buduo CA, Balduini A (2013) "Involvement of TGFß1 in autocrine regulation of proplatelet formation in healthy subjects and patients with primary myelofibrosis"

Priori SG. (2013) "KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia."

G. Palladini (2013) "Light chain amyloidosis 2012: a new era."

Crotti L., Ghidoni A. (2013) "Long QT syndrome-associated mutations in intrauterine fetal death."

F. Novara, O. Zuffardi (2013) "MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features."

Ermanno Gherardi (2013) "Michael Stoker 1918–2013"

Pietrocola G, Rindi S, Di Poto A, Speziale P (2013) "Molecular characterization of the multiple interactions of SpsD, a surface protein from Staphylococcus pseudintermedius, with host extracellular matrix proteins "

Mangione PP, Giorgetti S, Stoppini M, Bellotti V (2013) "Monitoring the interaction between ß2-microglobulin and the molecular chaperone aB-crystallin by NMR and mass spectrometry: aB-crystallin dissociates ß2-microglobulin oligomers."

O. Zuffardi (2013) "Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1."

Savio M, Forlino A (2013) "Multiple effects of the Na(+)/H (+) antiporter inhibitor HMA on cancer cells."

Cazzola M (2013) "Mutations and prognosis in primary myelofibrosis"

O. Zuffardi, G. Camerino (2013) "Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/ß-catenin signaling."

Cazzola M (2013) "NOTCH1, SF3B1, and TP53 mutations in fludarabine-refractory CLL patients treated with alemtuzumab: results from the CLL2H trial of the GCLLSG"

Malcovati L, Cazzola M (2013) "Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome"

O. Zuffardi (2013) "Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement."

Mangione PP (2013) "Pathogenetic mechanisms of amyloid A amyloidosis."

F. Novara, O. Zuffardi (2013) "Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene."

Roberto Bottinelli (2013) "Physiological and functional evaluation of healthy young and older men and women: design of the European MyoAge study"

O. Zuffardi (2013) "Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH."

G. Palladini, G. Merlini (2013) "Primary therapy of Waldenstrom macroglobulinemia (WM) with weekly bortezomib, low-dose dexamethasone, and rituximab (BDR): long-term results of a phase 2 study of the European Myeloma Network (EMN)."

Giorgetti S, Stoppini M, Bellotti V (2013) "Reduction of conformational mobility and aggregation in W60G ß2-microglobulin: assessment by 15N NMR relaxation."

G. Palladini, G. Merlini (2013) "Reply to S. Girnius et al."

Cazzola M (2013) "Retinoic acid and arsenic trioxide for acute promyelocytic leukemia"

F. Passamonti (2013) "Revised response criteria for myelofibrosis: International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) and European LeukemiaNet (ELN) consensus report"

F. Passamonti (2013) "Revised response criteria for polycythemia vera and essential thrombocythemia: an ELN and IWG-MRT consensus project"

Malcovati L, Cazzola M (2013) "Role of reduced-intensity conditioning allogeneic hematopoietic stem-cell transplantation in older patients with de novo myelodysplastic syndromes: an international collaborative decision analysis"

R. Bottinelli (2013) "Skeletal muscle adaptations to physical inactivity and subsequent retraining in young men"

Malcovati L, Cazzola M (2013) "Somatic mutations of calreticulin in myeloproliferative neoplasms"

Speziale P (2013) "Sortase A promotes virulence in experimental Staphylococcus lugdunensis endocarditis."

G. Palladini, G. Merlini (2013) "Stanniocalcin1 is a key mediator of amyloidogenic light chain induced cardiotoxicity."

Bellotti V (2013) "Structure of an early native-like intermediate of ß2-microglobulin amyloidogenesis."

Mangione PP, Raimondi S, Giorgetti S, Stoppini M, Bellotti V (2013) "Structure, folding dynamics and amyloidogenesis of Asp76Asn ß2-microglobulin: roles of shear flow, hydrophobic surfaces and a crystallin."

Cazzola M, Passamonti F (2013) "Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study."

G. Merlini, G. Palladini (2013) "Systemic light chain amyloidosis: an update for treating physicians."

Vercellino M, Visai L (2013) "Ternary PVA nanocomposites containing cellulose nanocrystals from different sources and silver particles: part II."

Cazzola M (2013) "The ERCC2 Gln/Gln polymorphism at codon 751 is not associated with leukaemic transformation in primary myelofibrosis"

Corsico AG (2013) "The cost of persistent asthma in Europe: an international population-based study in adults."

Cazzola M (2013) "The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts"

F. Passamonti (2013) "Three-year efficacy, safety, and survival findings from COMFORT-II, a phase 3 study comparing ruxolitinib with best available therapy for myelofibrosis"

I. Ferrarotti, M. Luisetti (2013) "a1-Antitrypsin level and pheno/genotypes"

Malpasso G (2013) "MicroRNA133 and microRNA499 exert synergistic effect on cardiac differentation."

Malpasso G (2013) "Pentraxin-3 and Galectin-1 are key mediators of the cardioprotective paracrine effects exerted by fetal mesenchymal stem cells isolated from human placenta"