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Bio-optical modeling of primary production on regional scales: the Bermuda BioOptics project

Deep-sea research. Part II, Topical studies in oceanography, 2001, Vol.48 (8), p.1865-1896

2001

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effect of biomass density, temperature, and substrate on transport survival of market-size freshwater prawn, Macrobrachium rosenbergii

Journal of applied aquaculture, 2005, Vol.17 (4), p.61-71

2005

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Diagnostic value of a comprehensive, urothelial carcinoma–specific next‐generation sequencing panel in urine cytology and bladder tumor specimens

Cancer cytopathology, 2021-07, Vol.129 (7), p.537-547

2021

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Is cellular senescence involved in cystic fibrosis?

Respiratory research, 2019-02, Vol.20 (1), p.32-32, Article 32

2019

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P477 How the use of nocturnal non-invasive ventilation and oxygen therapy changes in patients with cystic fibrosis using elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2024-06, Vol.23, p.S213-S213

2024

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P040 Sweat chloride values in cystic fibrosis patients after one year on elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2023-06, Vol.22, p.S75-S75

2023

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P113 Microbiology assessment in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2022-06, Vol.21, p.S96

2022

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P162 Body composition assessment in cystic fibrosis (CF) patients on elexacaftor/texacaftor/ivacaftor

Journal of cystic fibrosis, 2022-06, Vol.21, p.S110-S111

2022

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Two novel and correlated CF-causing insertions in the (TG)mTn tract of the CFTR gene

PloS one, 2019-10, Vol.14 (10), p.e0222838-e0222838

2019

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P466 Yoga in children with cystic fibrosis: complementary therapy alternative to the yoga practice in the presence

Journal of cystic fibrosis, 2024-06, Vol.23, p.S210-S210

2024

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P348 Nutritional challenges in the era of cystic fibrosis transmembrane regulator modulators: can we still trust the body mass index?

Journal of cystic fibrosis, 2024-06, Vol.23, p.S175-S175

2024

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P007 A novel cystic fibrosis-causing mutation identified in a newborn of African origin

Journal of cystic fibrosis, 2021, Vol.20, p.S40-S41

2021

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P330 One-year assessment of body composition in cystic fibrosis patients on elexacaftor/texacaftor/ivacaftor

Journal of cystic fibrosis, 2023-06, Vol.22, p.S165-S166

2023

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P413 How to use telemonitoring for the detection of respiratory exacerbations in cystic fibrosis: effectiveness and adherence

Journal of cystic fibrosis, 2023-06, Vol.22, p.S190-S190

2023

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P032 Sweat chloride values in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2022-06, Vol.21, p.S69

2022

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Safety of Oats in Children with Celiac Disease: A Double-Blind, Randomized, Placebo-Controlled Trial

The Journal of pediatrics, 2018-03, Vol.194, p.116-122.e2

2018

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Somatic molecular analysis augments cytologic evaluation of pancreatic cyst fluids as a diagnostic tool

Oncotarget, 2019-06, Vol.10 (40), p.4026-4037

2019

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Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells

British journal of haematology, 2024-01, Vol.204 (1), p.292-305

2024

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Two novel and correlated CF-causing insertions in the

PloS one, 2019-10, Vol.14 (10), p.e0222838

2019

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Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype

Journal of cystic fibrosis, 2022-09, Vol.21 (5), p.850-855

2022

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Nutrition in infants undergoing surgery for congenital heart disease. A longitudinal study in 71 children

Digestive and liver disease, 2016-10, Vol.48, p.e278-e279

2016

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111 Non-tuberculous mycobacteria in patients with cystic fibrosis: detection and isolation from respiratory samples. Results of a cross-sectional study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S93-S93

2017

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P020 CFTR mutation panel in detecting cystic fibrosis screen positive inconclusive diagnosis patients (CFSPIDs) in the Marche Region, Italy

Journal of cystic fibrosis, 2021, Vol.20, p.S44

2021

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Cervista HR and HPV 16/18 Assays vs Hybrid Capture 2 Assay: Outcome Comparison in Women With Negative Cervical Cytology

American journal of clinical pathology, 2011-11, Vol.136 (5), p.808-816

2011

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291 Colon cancer screening program in adult CF patients: an Italian cross-sectional pilot study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S136-S136

2017

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Bio-optical modeling of primary production on regional scales: the Bermuda BioOptics project

effect of biomass density, temperature, and substrate on transport survival of market-size freshwater prawn, Macrobrachium rosenbergii

Diagnostic value of a comprehensive, urothelial carcinoma–specific next‐generation sequencing panel in urine cytology and bladder tumor specimens

Is cellular senescence involved in cystic fibrosis?

P477 How the use of nocturnal non-invasive ventilation and oxygen therapy changes in patients with cystic fibrosis using elexacaftor/tezacaftor/ivacaftor

P040 Sweat chloride values in cystic fibrosis patients after one year on elexacaftor/tezacaftor/ivacaftor

P113 Microbiology assessment in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor

P162 Body composition assessment in cystic fibrosis (CF) patients on elexacaftor/texacaftor/ivacaftor

Two novel and correlated CF-causing insertions in the (TG)mTn tract of the CFTR gene

P466 Yoga in children with cystic fibrosis: complementary therapy alternative to the yoga practice in the presence

P348 Nutritional challenges in the era of cystic fibrosis transmembrane regulator modulators: can we still trust the body mass index?

P007 A novel cystic fibrosis-causing mutation identified in a newborn of African origin

P330 One-year assessment of body composition in cystic fibrosis patients on elexacaftor/texacaftor/ivacaftor

P413 How to use telemonitoring for the detection of respiratory exacerbations in cystic fibrosis: effectiveness and adherence

P032 Sweat chloride values in cystic fibrosis patients on elexacaftor/tezacaftor/ivacaftor

Safety of Oats in Children with Celiac Disease: A Double-Blind, Randomized, Placebo-Controlled Trial

Somatic molecular analysis augments cytologic evaluation of pancreatic cyst fluids as a diagnostic tool

Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells

Two novel and correlated CF-causing insertions in the

Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype

Nutrition in infants undergoing surgery for congenital heart disease. A longitudinal study in 71 children

111 Non-tuberculous mycobacteria in patients with cystic fibrosis: detection and isolation from respiratory samples. Results of a cross-sectional study

P020 CFTR mutation panel in detecting cystic fibrosis screen positive inconclusive diagnosis patients (CFSPIDs) in the Marche Region, Italy

Cervista HR and HPV 16/18 Assays vs Hybrid Capture 2 Assay: Outcome Comparison in Women With Negative Cervical Cytology

291 Colon cancer screening program in adult CF patients: an Italian cross-sectional pilot study

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