Search Results - "Bredi, Elena"

Serum ANCA and Overall Mortality: A 10-Year Retrospective Cohort Study on 1,024 Italian Subjects by Brunetta, Enrico, Ramponi, Giacomo, Folci, Marco, De Santis, Maria, Morenghi, Emanuela, Vanni, Elena, Bredi, Elena, Furlan, Raffaello, Angelini, Claudio, Selmi, Carlo

“…Antineutrophil cytoplasmic antibodies (ANCA) are primarily involved in the pathogenesis of ANCA-associated vasculitides (AAV). However, ANCA may also be…”
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Overcoming a “Probable” Diagnosis in Antimitochondrial Antibody Negative Primary Biliary Cirrhosis: Study of 100 Sera and Review of the Literature by Bizzaro, Nicola, Covini, Giovanni, Rosina, Floriano, Muratori, Paolo, Tonutti, Elio, Villalta, Danilo, Pesente, Fiorenza, Alessio, Maria Grazia, Tampoia, Marilina, Antico, Antonio, Platzgummer, Stefan, Porcelli, Brunetta, Terzuoli, Lucia, Liguori, Marco, Bassetti, Danila, Brusca, Ignazio, Almasio, Piero L., Tarantino, Giuseppe, Bonaguri, Chiara, Agostinis, Paolo, Bredi, Elena, Tozzoli, Renato, Invernizzi, Pietro, Selmi, Carlo

“…Serum anti-mitochondrial antibodies (AMA) are the serological hallmark of primary biliary cirrhosis (PBC), yet up to 15% of PBC sera are AMA negative at…”
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Autoimmune Hepatitis During Ledipasvir/Sofosbuvir Treatment of Hepatitis C: A Case Report by Covini, Giovanni, Bredi, Elena, Badalamenti, Salvatore, Roncalli, Massimo, Aghemo, Alessio, Colombo, Massimo

“…We report the case of a woman with chronic hepatitis C and idiopathic thrombocytopenic purpura (ITP) who developed autoimmune hepatitis (AIH) during antiviral…”
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Cytoplasmic rods and rings in ribavirin treatment by Covini, Giovanni, Bredi, Elena

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A variant of the EPB3 gene of the anti‐Lepore type in hereditary spherocytosis by Bianchi, Paola, Zanella, Alberto, Alloisio, Nicole, Barosi, Giovanni, Bredi, Elena, Pelissero, Giovanni, Zappa, Manuela, Vercellati, Cristina, Baronciani, Luciano, Delaunay, Jean, Sirchia, Girolamo

“…The EPB3 gene encodes band 3 (anion exchanger 1) of the red cell membrane. A subset of hereditary spherocytosis (HS) is associated with EPB3 gene mutations and…”
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Cytoplasmic rods and rings autoantibodies developed during pegylated interferon and ribavirin therapy in patients with chronic hepatitis C by Covini, Giovanni, Carcamo, Wendy C, Bredi, Elena, von Mühlen, Carlos A, Colombo, Massimo, Chan, Edward K L

“…Serum autoantibodies are frequently detected in patients with chronic HCV infection, reflecting the wide spectrum of immune reactions related to this virus. In…”
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Changes in viremia and circulating interferon-α during hemodialysis in hepatitis C virus-positive patients: only coincidental phenomena? by Badalamenti, Salvatore, Catania, Anna, Lunghi, Giovanna, Covini, Giovanni, Bredi, Elena, Brancaccio, Diego, Salvadori, Maurizio, Como, Giovanna, Ponticelli, Claudio, Graziani, Giorgio

“…It has been hypothesized that hemodialysis (HD) treatment per se can preserve patients from an aggressive course of hepatitis C virus (HCV) infection by…”
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A case of complete adenylate kinase deficiency due to a nonsense mutation in AK‐1 gene (Arg 107 → Stop, CGA → TGA) associated with chronic haemolytic anaemia by Bianchi, Paola, Zappa, Manuela, Bredi, Elena, Vercellati, Cristina, Pelissero, Giovanni, Barraco, Fiorenza, Zanella, Alberto

“…Two siblings of Italian origin with mild chronic haemolytic anaemia, psychomotor impairment and undetectable adenylate kinase (AK) activity are reported. The…”
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Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients by Zanella, Alberto, Bianchi, Paola, Baronciani, Luciano, Zappa, Manuela, Bredi, Elena, Vercellati, Cristina, Alfinito, Fiorella, Pelissero, Giovanni, Sirchia, Girolamo

“…We studied the PK-LR gene in 15 unrelated Italian patients with congenital hemolytic anemia associated with erythrocyte pyruvate kinase (PK) deficiency…”
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Molecular characterization of PK-LR gene in pyruvate kinase-deficient Italian patients by ZANELLA, A, BIANCHI, P, BARONCIANI, L, ZAPPA, M, BREDI, E, VERCELLATI, C, ALFINITO, F, PELISSERO, G, SIRCHIA, G

“…We studied the PK-LR gene in 15 unrelated Italian patients with congenital hemolytic anemia associated with erythrocyte pyruvate kinase (PK) deficiency…”
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A case of complete adenylate kinase deficiency due to a nonsense mutation in AK-1 gene (Arg 107→Stop, CGA→TGA) associated with chronic haemolytic anaemia by BIANCHI, P, ZAPPA, M, BREDI, E, VERCELLATI, C, PELISSERO, G, BARRACO, F, ZANELLA, A

“…Two siblings of Italian origin with mild chronic haemolytic anaemia, psychomotor impairment and undetectable adenylate kinase (AK) activity are reported. The…”
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