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Marta Miorin

Circulating Endothelial Progenitor Cells Are Reduced in Peripheral Vascular Complications of Type 2 Diabetes Mellitus
2005 · Gian Paolo Fadini, Marta Miorin, et al. · Journal of the American College of Cardiology · 726
Chronic lymphocytic leukemia B cells contain anomalous Lyn tyrosine kinase, a putative contribution to defective apoptosis
2005 · Antonella Contri, Anna Maria Brunati, et al. · Journal of Clinical Investigation · 260
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Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy
1996 · P. Melacini, M. Fanin, et al. · Circulation · 196
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample
2009 · ML Mostacciuolo, E Pastorello, et al. · Clinical Genetics · 170
ARVD4, a New Locus for Arrhythmogenic Right Ventricular Cardiomyopathy, Maps to Chromosome 2 Long Arm
1997 · Alessandra Rampazzo, Andrea Nava, et al. · Genomics · 170
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Homeostatic chemokines drive migration of malignant B cells in patients with non-Hodgkin lymphomas
2004 · Livio Trentin, Anna Cabrelle, et al. · Blood · 148
Circulating Progenitor Cells Are Reduced in Patients with Severe Lung Disease
2006 · Gian Paolo Fadini, Marco Schiavon, et al. · Stem Cells · 145
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy
1996 · P. Melacini, A. Vianello, et al. · Neuromuscular Disorders · 142
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy
1996 · Maria L. Mostacciuolo, Marta Miorin, et al. · Human Genetics · 126
Role for CXCR6 and Its Ligand CXCL16 in the Pathogenesis of T-Cell Alveolitis in Sarcoidosis
2005 · Carlo Agostini, Anna Cabrelle, et al. · American Journal of Respiratory and Critical Care Medicine · 87
Epidemiology of myotonic dystrophy in Italy: re‐apprisal after genetic diagnosis
2001 · G Siciliano, ML Manca, et al. · Clinical Genetics · 70
Dystrophin‐positive fibers in duchenne dystrophy: Origin and correlation to clinical course
1995 · Marina Fanin, Gian Antonio Danieli, et al. · Muscle & Nerve · 70
Expression and role of CCR6/CCL20 chemokine axis in pulmonary sarcoidosis
2007 · Monica Facco, Ilenia Baesso, et al. · Journal of Leukocyte Biology · 54
Prognostic factors in mild dystrophinopathies
1996 · C Angelini, M Fanin, et al. · Journal of the Neurological Sciences · 52
Multiple myeloma plasma cells show different chemokine receptor profiles at sites of disease activity
2007 · Livio Trentin, Marta Miorin, et al. · British Journal of Haematology · 47
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Genotypic evaluation of killer immunoglobulin-like receptors in NK-type lymphoproliferative disease of granular lymphocytes
2007 · E Scquizzato, A Teramo, et al. · Leukemia · 44
Epithelial CXCR3-B Regulates Chemokines Bioavailability in Normal, but Not in Sjogren’s Syndrome, Salivary Glands
2006 · Paolo Sfriso, Francesca Oliviero, et al. · The Journal of Immunology · 43
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CXCR3/CXCL10 interactions in the development of hypersensitivity pneumonitis
2005 · Carlo Agostini, Fiorella Calabrese, et al. · Respiratory Research · 31
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Phenotypic and functional analyses of dendritic cells in patients with lymphoproliferative disease of granular lymphocytes (LDGL)
2005 · Renato Zambello, Tamara Berno, et al. · Blood · 30
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Lack of expression of inhibitory KIR3DL1 receptor in patients with natural killer cell-type lymphoproliferative disease of granular lymphocytes
2010 · C. Gattazzo, A. Teramo, et al. · Haematologica · 28
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HCV-related liver and lymphoproliferative diseases: association with polymorphisms of IL28B and TLR2
2016 · Valli De Re, Mariangela De Zorzi, et al. · Oncotarget · 27
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Reappraisal of the Incidence Rate of Duchenne and Becker Muscular Dystrophies on the Basis of Molecular Diagnosis
1993 · M.L. Mostacciuolo, M. Miorin, et al. · Neuroepidemiology · 24
T cells in the lung of patients with hypersensitivity pneumonitis accumulate in a clonal manner
2004 · Monica Facco, Livio Trentin, et al. · Journal of Leukocyte Biology · 20
Prevalent cardiac involvement in dystrophin Becker type mutation
1994 · G. Siciliano, M. Fanin, et al. · Neuromuscular Disorders · 16
A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron
1994 · Federico Galvagni, Fawzy A. Saad, et al. · Human Genetics · 16
Works count: 64
Citation count: 2,827
H-index: 22
I10-index: 27
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