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Lung clearance index short-term variability in cystic fibrosis: a pre-post pulmonary exacerbation study

Italian journal of pediatrics, 2024-01, Vol.50 (1), p.6-6, Article 6

2024

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Metabolomic Analysis by Nuclear Magnetic Resonance Spectroscopy as a New Approach to Understanding Inflammation and Monitoring of Pharmacological Therapy in Children and Young Adults With Cystic Fibrosis

Frontiers in pharmacology, 2018-06, Vol.9, p.595-595

2018

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The Challenging Life of Mutators: How Pseudomonas aeruginosa Survives between Persistence and Evolution in Cystic Fibrosis Lung

Microorganisms (Basel), 2024-10, Vol.12 (10), p.2051

2024

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Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis

Molecular medicine (Cambridge, Mass.), 2016-01, Vol.22 (1), p.300-309

2016

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Longitudinal Effects of Elexacaftor/Tezacaftor/Ivacaftor: Multidimensional Assessment of Neuropsychological Side Effects and Physical and Mental Health Outcomes in Adolescents and Adults

Chest, 2024-04, Vol.165 (4), p.800-809

2024

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Longitudinal Effects of Elexacaftor/Tezacaftor/Ivacaftor

Chest, 2024-04, Vol.165 (4), p.800-809

2024

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A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome

The Journal of pediatrics, 2020-04, Vol.219, p.196-201.e1

2020

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Aryl Hydrocarbon Receptor Agonism Antagonizes the Hypoxia-driven Inflammation in Cystic Fibrosis

American journal of respiratory cell and molecular biology, 2023-03, Vol.68 (3), p.288-301

2023

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Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis

Pediatric pulmonology, 2015-02, Vol.50 (2), p.144-149

2015

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Nuclear Magnetic Resonance―based Metabolomics Discriminates Primary Ciliary Dyskinesia from Cystic Fibrosis

American journal of respiratory and critical care medicine, 2014-07, Vol.190 (2), p.229-233

2014

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The effect of inhaled hypertonic saline on lung structure in children aged 3–6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial

The lancet respiratory medicine, 2022-07, Vol.10 (7), p.669-678

2022

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Environmental Microbial Contamination during Cystic Fibrosis Group-Based Psychotherapy

International journal of environmental research and public health, 2021-01, Vol.18 (3), p.1142

2021

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An inflammatory Signature of Glucose Impairment in Cystic Fibrosis

Journal of inflammation research, 2022-10, Vol.15, p.5677-5685

2022

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NREM sleep instability is reduced in children with attention-deficit/hyperactivity disorder

Sleep (New York, N.Y.), 2006-06, Vol.29 (6), p.797-803

2006

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Fewer spontaneous arousals in infants with apparent life-threatening event

Sleep (New York, N.Y.), 2011-06, Vol.34 (6), p.733-743

2011

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Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis: Cystic Fibrosis-Related Diabetes and Pubertal Growth

Pediatric pulmonology, 2015-02, Vol.50 (2), p.144-149

2015

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Maturation of arousals during day and night in infants with non-smoking and smoking mothers

Early human development, 2017-12, Vol.115, p.46-50

2017

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ZnT8 antibodies in patients with cystic fibrosis: An expression of secondary beta-cell damage?

Journal of cystic fibrosis, 2013-12, Vol.12 (6), p.803-805

2013

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Immunogenicity and safety profile of the monovalent A/H1N1 MF59-adjuvanted vaccine in patients affected by cystic fibrosis

Thorax, 2011-03, Vol.66 (3), p.259-260

2011

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Streptococcus pneumoniae oropharyngeal colonization in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2016-05, Vol.15 (3), p.366-371

2016

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Sudden Infant Death Syndrome from Epidemiology to Pathophysiology

Current pediatric reviews, 2007-08, Vol.3 (3), p.177-189

2007

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Validation of a predictive survival model in Italian patients with cystic fibrosis

Journal of cystic fibrosis, 2012-01, Vol.11 (1), p.24-29

2012

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Arousal from sleep mechanisms in infants

Sleep medicine, 2010-08, Vol.11 (7), p.603-614

2010

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Mortality rate of patients with cystic fibrosis on the waiting list and within one year after lung transplantation: a survey of Italian CF centers

Italian journal of pediatrics, 2018-06, Vol.44 (1), p.72-72, Article 72

2018

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Spontaneous arousability in prone and supine position in healthy infants

Sleep (New York, N.Y.), 2006-06, Vol.29 (6), p.785-790

2006

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Lung clearance index short-term variability in cystic fibrosis: a pre-post pulmonary exacerbation study

Metabolomic Analysis by Nuclear Magnetic Resonance Spectroscopy as a New Approach to Understanding Inflammation and Monitoring of Pharmacological Therapy in Children and Young Adults With Cystic Fibrosis

The Challenging Life of Mutators: How Pseudomonas aeruginosa Survives between Persistence and Evolution in Cystic Fibrosis Lung

Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis

Longitudinal Effects of Elexacaftor/Tezacaftor/Ivacaftor: Multidimensional Assessment of Neuropsychological Side Effects and Physical and Mental Health Outcomes in Adolescents and Adults

Longitudinal Effects of Elexacaftor/Tezacaftor/Ivacaftor

A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome

Aryl Hydrocarbon Receptor Agonism Antagonizes the Hypoxia-driven Inflammation in Cystic Fibrosis

Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis

Nuclear Magnetic Resonance―based Metabolomics Discriminates Primary Ciliary Dyskinesia from Cystic Fibrosis

The effect of inhaled hypertonic saline on lung structure in children aged 3–6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial

Environmental Microbial Contamination during Cystic Fibrosis Group-Based Psychotherapy

An inflammatory Signature of Glucose Impairment in Cystic Fibrosis

NREM sleep instability is reduced in children with attention-deficit/hyperactivity disorder

Fewer spontaneous arousals in infants with apparent life-threatening event

Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis: Cystic Fibrosis-Related Diabetes and Pubertal Growth

Maturation of arousals during day and night in infants with non-smoking and smoking mothers

ZnT8 antibodies in patients with cystic fibrosis: An expression of secondary beta-cell damage?

Immunogenicity and safety profile of the monovalent A/H1N1 MF59-adjuvanted vaccine in patients affected by cystic fibrosis

Streptococcus pneumoniae oropharyngeal colonization in children and adolescents with cystic fibrosis

Sudden Infant Death Syndrome from Epidemiology to Pathophysiology

Validation of a predictive survival model in Italian patients with cystic fibrosis

Arousal from sleep mechanisms in infants

Mortality rate of patients with cystic fibrosis on the waiting list and within one year after lung transplantation: a survey of Italian CF centers

Spontaneous arousability in prone and supine position in healthy infants

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