Simona Cristadoro

COVID-19 in people with Cystic Fibrosis beyond the pre-omicron era: a prospective study with a specific focus on long COVID

Carla Colombo, Paola Medino, Marco Cipolli, Francesca Lucca et autres

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P159 Long COVID in people with cystic fibrosis: a prospective observational study within the Italian Cystic Fibrosis Society

C. Colombo, P. Medino, Giovanni Taccetti, F. Lucca et autres

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Raman Spectroscopy and Cystic Fibrosis Disease: An Alternative Potential Tool for Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulator Response Differentiation—A Pilot Study Based on Serum Samples

Giuseppe Acri, Barbara Testagrossa, Maria Cristina Lucanto, Simona Cristadoro et autres

Cystic fibrosis (CF) is a genetic disorder that alters chloride transport in mucous membranes. Recent studies have demonstrated that treatment with modulators of the chloride channel reduces inflammatory markers, restoring, among others, the imbalance of lipids. In this study, we analyzed the …

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Rescue by elexacaftor-tezacaftor-ivacaftor of the G1244E cystic fibrosis mutation's stability and gating defects are dependent on cell background

Valeria Tomati, Stefano Costa, Valeria Capurro, Emanuela Pesce et autres

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Malassezia Folliculitis following Triple Therapy for Cystic Fibrosis

Federica Li Pomi, Luca Di Bartolomeo, Mario Vaccaro, Maria Lentini et autres

mutation in the transmembrane conductance regulator of the cystic fibrosis gene. Among the adverse events of elexacaftor, tezacaftor and ivacaftor, the cutaneous ones have been rarely reported, mainly dealing with urticarial-like rashes. On this topic, we report two cases of Malassezia folliculitis …

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P134 SARS-CoV-2 infection in cystic fibrosis during the first pandemic wave in Italy: a multi-centre prospective study with a control group

Carlo Colombo, Gianfranco Alicandro, Valeria Daccò, Vanessa Gagliano et autres

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C3 glomerulopathy in cystic fibrosis: a case report

Domenico Santoro, Rossella Siligato, Carmela Vadalà, Mariacristina Lucanto et autres

BACKGROUND: C3 glomerulonephritis is a rare glomerulopathy characterized at renal biopsy by C3 deposition, alone or with scanty immunoglobulins, as well as by an electron-dense material in mesangium, subendothelial and subepithelial space. An abnormal systemic activation of the alternative pathway of the …

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Cystic Fibrosis: A Risk Condition for Renal Disease

Domenico Santoro, Adele Postorino, Cristina Lucanto, Stefano Costa et autres

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Mycobacterium abscessusin patients with cystic fibrosis: low impact of inter-human transmission in Italy

Enrico Tortoli, Thomas A. Kohl, Alberto Trovato, Rossella Baldan et autres

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Bronchial tree‐shaped mucous plug in cystic fibrosis: imaging‐guided management

Ignazio Salamone, B Mondello, Maria Cristina Lucanto, Simona Cristadoro et autres

We report the case of a 17‐year‐old boy with cystic fibrosis (CF) who presented with persistent cough; after starting intravenous antibiotics for Pseudomonas aeruginosa he underwent a computed tomography (CT) scan of the chest. CT revealed extensive consolidation in the right lower …

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Renal amyloidosis in cystic fibrosis: role of colchicine therapy

Domenico Santoro, Adele Postorino, Stefano Costa, Simona Cristadoro et autres

Cystic fibrosis (CF) is the most common autosomal-recessive condition affecting the white population, with an incidence ranging between 1:2500 and 1:1800 births. It is caused by a mutation in the CFTR gene, encoding the polyprotein CF transmembrane conductance regulator (CFTR), which functions …

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Clinical nephrology - miscellaneous

Christos Bantis, P. Heering, N.-M. Kouri, M. Siekierka-Harreis et autres

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