Search Results - "Terlizzi, V."
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Elexacaftor/Tezacaftor/Ivacaftor therapy in cystic fibrosis children previously CFSPID: Is it over-medicalization?
Published in Journal of cystic fibrosis (01-03-2024)Get full text
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2
Achromobacter xylosoxidans respiratory tract infection in cystic fibrosis patients
Published in European journal of clinical microbiology & infectious diseases (01-08-2011)“…The aims of this study were to evaluate the frequency of Achromobacter xylosoxidans infection in a cohort of cystic fibrosis patients, to investigate…”
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3
Hidden CFSPID in CF patient registries? The Italian CF Registry experience
Published in Journal of cystic fibrosis (01-11-2023)Get full text
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4
Clinical characteristics and outcome of SARS –CoV-2 infection in patients with cystic fibrosis managed at home
Published in Pulmonology (01-03-2022)Get full text
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5
Risk of CFTR-related disorders and cystic fibrosis in an Italian cohort of CRMS/CFSPID subjects in preschool and school age
Published in European journal of pediatrics (01-02-2024)“…The identification of cystic fibrosis screening-positive, inconclusive diagnosis (CFSPID) in infants is a controversial outcome of newborn screening for cystic…”
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Hyperbilirubinemia and Gilbert's syndrome in Cystic Fibrosis patients treated with elexacaftor/tezacaftor/ivacaftor
Published in Journal of cystic fibrosis (01-11-2023)“…•Gilbert's syndrome testing is needed for post-ETI hyperbilirubinemia.•ETI therapy is safe for Gilbert's syndrome-related hyperbilirubinemia.•More research is…”
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7
Unilateral temporary diaphragmatic paralysis secondary to bronchial artery embolization in a girl with cystic fibrosis and massive hemoptysis: a case report
Published in BMC pulmonary medicine (11-02-2020)“…Massive hemoptysis is a serious complication in Cystic Fibrosis (CF), occurring commonly in older patients. Bronchial artery embolization (BAE) can be…”
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Elevated sweat chloride test: is it always cystic fibrosis?
Published in Italian journal of pediatrics (14-05-2021)“…The sweat chloride test (ST) is the gold standard for cystic fibrosis (CF) diagnosis in symptomatic patients, within the newborn screening and in the follow-up…”
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283 Cystic fibrosis-related diabetes screening: are there easy measures to implement the guidelines?
Published in Journal of cystic fibrosis (01-06-2017)Get full text
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Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis
Published in Journal of cystic fibrosis (01-09-2014)“…Abstract Background Currently no tools to predict risk of acute (AP) and recurrent pancreatitis (ARP) in children with cystic fibrosis (CF) are available. We…”
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428 Are cystic fibrosis guidelines credible? Evaluating methodological issues
Published in Journal of cystic fibrosis (01-06-2017)Get full text
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WS21.3 Clinical variability in patients with cystic fibrosis and D1152H mutation
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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10 The role of complex alleles in patients with cystic fibrosis and L997F
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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225 PIP score could predict the risk of pancreatitis in patients with cystic fibrosis (CF)?
Published in Journal of cystic fibrosis (01-06-2012)Get full text
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CO14 INDIVIDUAL MANAGEMENT IMPROVES NUTRITIONAL OUTCOMES IN PATIENTS WITH CYSTIC FIBROSIS
Published in Digestive and liver disease (2011)Get full text
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PA57 ACUTE RECURRENT PANCREATITIS AND GENETIC RISK FACTORS: A CASE REPORT
Published in Digestive and liver disease (2010)Get full text
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Can an isolated hypertransaminasemia be dependent on a congenital disorder of glycosilation?
Published in Digestive and liver disease (2008)Get full text
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Asking for iodine supplementation in children on parenteral nutrition
Published in Digestive and liver disease (2008)Get full text
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A boy with UDCA-dependent hypertransaminasemia
Published in Digestive and liver disease (2008)Get full text
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