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Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles

Scientific reports, 2021-03, Vol.11 (1), p.6393-6393, Article 6393

2021

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TAS2R38 is a novel modifier gene in patients with cystic fibrosis

Scientific reports, 2020-04, Vol.10 (1), p.5806-5806, Article 5806

2020

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Intralabyrinthine Schwannoma of the Intravestibular Subtype: A Difficult Diagnosis

Ear, nose, & throat journal, 2022-06, Vol.101 (5), p.301-303

2022

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Computed-Tomography-Structured Reporting in Middle Ear Opacification: Surgical Results and Clinical Considerations From a Large Retrospective Analysis

Frontiers in neurology, 2021-02, Vol.12, p.615356-615356

2021

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Elexacaftor–Tezacaftor–Ivacaftor Therapy for Cystic Fibrosis Patients with The F508del/Unknown Genotype

Antibiotics (Basel), 2021-07, Vol.10 (7), p.828

2021

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Combining Thin-Section Coronal and Axial Diffusion Weighted Imaging: Good Practice in Middle Ear Cholesteatoma Neuroimaging

Frontiers in neurology, 2021-09, Vol.12, p.606692-606692

2021

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Letter to the Editor: Is there an Indication for Testing the Methylenetetrahydrofolate reductase A1298C Variant in Routine Clinical Settings?

Annals of clinical and laboratory science, 2021-03, Vol.51 (2), p.277-279

2021

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Quality of Life Assessment of Chronic Otitis Media Patients Following Surgery

Journal of personalized medicine, 2022-12, Vol.13 (1), p.74

2022

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Impact of the COVID-19 pandemic on paediatric otolaryngology: a nationwide study

Acta otorhino-laryngologica italica, 2023-10, Vol.43 (5), p.352-359

2023

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Cholesteatoma vs granulation tissue: a differential diagnosis by DWI-MRI apparent diffusion coefficient

European archives of oto-rhino-laryngology, 2018-09, Vol.275 (9), p.2237-2243

2018

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Clinical expression of cystic fibrosis in a large cohort of Italian siblings

BMC pulmonary medicine, 2018-12, Vol.18 (1), p.196-196, Article 196

2018

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S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy

Italian journal of pediatrics, 2018-01, Vol.44 (1), p.2-2, Article 2

2018

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High-Definition 3D Exoscope in Pediatric Otorhinolaryngology: A Systematic Literature Review

Journal of clinical medicine, 2023-10, Vol.12 (20), p.6528

2023

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Unusual Localization of an Emergent Bacterium, Raoultella ornithinolytica

Case reports in medicine, 2020, Vol.2020 (2020), p.1-3

2020

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Molecular Analysis of Prothrombotic Gene Variants in Venous Thrombosis: A Potential Role for Sex and Thrombotic Localization

Journal of clinical medicine, 2020-04, Vol.9 (4), p.1008

2020

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Immunohistochemical patterns in the differential diagnosis of rhinopharyngeal granulocytic sarcoma

Oncology letters, 2016-10, Vol.12 (4), p.2777-2781

2016

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Strategy for the treatment and follow-up of sinonasal solitary extramedullary plasmacytoma: a case series

Journal of medical case reports, 2017-08, Vol.11 (1), p.219-219, Article 219

2017

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Surgical treatment of unusual osteoma associated with homolateral radicular cyst of the maxillary sinus

Journal of oral medicine and oral surgery, 2020, Vol.26 (3), p.30

2020

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Cystic fibrosis, molecular genetics for all life

Journal of pediatric and neonatal individualized medicine, 2015-10, Vol.4 (2), p.e040252-e040252

2015

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Solitary Intraparotid Facial Nerve Plexiform Neurofibroma

International journal of clinical medicine, 2014-09, Vol.5 (18), p.1125-1125

2014

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Two CFTR mutations within codon 970 differently impact on the chloride channel functionality

Human mutation, 2019-06, Vol.40 (6), p.742-748

2019

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Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles

Journal of medical genetics, 2017-04, Vol.54 (4), p.224-235

2017

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Follow-up strategies in pediatric cholesteatoma: a systematic review

European archives of oto-rhino-laryngology, 2024-08

2024

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Prothrombotic gene variants in acute myocardial infarction at a young age (yAMI). Rationale for tailored prevention strategies in specific risk-group subjects for acute coronary disease?

Nutrition, metabolism, and cardiovascular diseases, 2020-07, Vol.30 (8), p.1397-1400

2020

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The CO2-laser in the treatment of laryngeal and tracheal stenosis Our personal experiences

Annali italiani di chirurgia, 2020, Vol.91, p.239

2020

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Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles

TAS2R38 is a novel modifier gene in patients with cystic fibrosis

Intralabyrinthine Schwannoma of the Intravestibular Subtype: A Difficult Diagnosis

Computed-Tomography-Structured Reporting in Middle Ear Opacification: Surgical Results and Clinical Considerations From a Large Retrospective Analysis

Elexacaftor–Tezacaftor–Ivacaftor Therapy for Cystic Fibrosis Patients with The F508del/Unknown Genotype

Combining Thin-Section Coronal and Axial Diffusion Weighted Imaging: Good Practice in Middle Ear Cholesteatoma Neuroimaging

Letter to the Editor: Is there an Indication for Testing the Methylenetetrahydrofolate reductase A1298C Variant in Routine Clinical Settings?

Quality of Life Assessment of Chronic Otitis Media Patients Following Surgery

Impact of the COVID-19 pandemic on paediatric otolaryngology: a nationwide study

Cholesteatoma vs granulation tissue: a differential diagnosis by DWI-MRI apparent diffusion coefficient

Clinical expression of cystic fibrosis in a large cohort of Italian siblings

S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy

High-Definition 3D Exoscope in Pediatric Otorhinolaryngology: A Systematic Literature Review

Unusual Localization of an Emergent Bacterium, Raoultella ornithinolytica

Molecular Analysis of Prothrombotic Gene Variants in Venous Thrombosis: A Potential Role for Sex and Thrombotic Localization

Immunohistochemical patterns in the differential diagnosis of rhinopharyngeal granulocytic sarcoma

Strategy for the treatment and follow-up of sinonasal solitary extramedullary plasmacytoma: a case series

Surgical treatment of unusual osteoma associated with homolateral radicular cyst of the maxillary sinus

Cystic fibrosis, molecular genetics for all life

Solitary Intraparotid Facial Nerve Plexiform Neurofibroma

Two CFTR mutations within codon 970 differently impact on the chloride channel functionality

Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles

Follow-up strategies in pediatric cholesteatoma: a systematic review

Prothrombotic gene variants in acute myocardial infarction at a young age (yAMI). Rationale for tailored prevention strategies in specific risk-group subjects for acute coronary disease?

The CO2-laser in the treatment of laryngeal and tracheal stenosis Our personal experiences

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