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STEM undergraduates’ perspectives of instructor and university responses to the COVID-19 pandemic in Spring 2020

PloS one, 2021-08, Vol.16 (8), p.e0256213-e0256213

2021

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The role of institutional factors and cognitive absorption on students’ satisfaction and performance in online learning during COVID 19

PloS one, 2022-06, Vol.17 (6), p.e0269609-e0269609

2022

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Measuring student motivation on the use of a mobile assisted grammar learning tool

PloS one, 2020-08, Vol.15 (8), p.e0236862-e0236862

2020

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Predicting the intention to adopt wearable payment devices in China: The use of hybrid SEM-Neural network approach

PloS one, 2022-08, Vol.17 (8), p.e0273849-e0273849

2022

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“A friend during troubled times”: Experiences of family caregivers to persons with dementia when receiving professional support via a mobile app

PloS one, 2022-08, Vol.17 (8), p.e0271972-e0271972

2022

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User acceptance of voice biometrics in managing the physical access to a secure area of an international airport

Technology analysis & strategic management, 2020-10, Vol.32 (10), p.1236-1250

2020

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Global profiling of alternative splicing events and gene expression regulated by hnRNPH/F

PloS one, 2012-12, Vol.7 (12), p.e51266-e51266

2012

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Investigation of modifier genes within copy number variations in Rett syndrome

Journal of human genetics, 2011-07, Vol.56 (7), p.508-515

2011

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Households technology adoption and use patterns: the case of digital terrestrial television in six Italian regions

Technology analysis & strategic management, 2016-01, Vol.28 (1), p.40-59

2016

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p39, the Primary Activator for Cyclin-dependent Kinase 5 (Cdk5) in Oligodendroglia, Is Essential for Oligodendroglia Differentiation and Myelin Repair

The Journal of biological chemistry, 2013-06, Vol.288 (25), p.18047-18057

2013

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13q Deletion Syndrome Involving RB1 : Characterization of a New Minimal Critical Region for Psychomotor Delay

Genes, 2021-08, Vol.12 (9), p.1318

2021

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Ocular Surface Microbiota in Naïve Keratoconus: A Multicenter Validation Study

Journal of clinical medicine, 2023-10, Vol.12 (19), p.6354

2023

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Ocular microbiome evaluation in dry eye disease and meibomian gland dysfunction: Values of variables

Experimental eye research, 2023-11, Vol.236, p.109656-109656, Article 109656

2023

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FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2024-03, p.e32970-e32970

2024

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MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype

European journal of medical genetics, 2020-01, Vol.63 (1), p.103627-103627, Article 103627

2020

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Acceptance of Information and Communication Technologies for Healthy and Active Aging: Results from Three Field Studies

OBM Geriatrics, 2018-10, Vol.3 (1), p.1-1

2018

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AAV-mediated FOXG1 gene editing in human Rett primary cells

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1446-1458

2020

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Low‐level TP 53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia

British journal of haematology, 2019-02, Vol.184 (4), p.657-659

2019

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Abstract 1311: Notch1 inhibits retinoblastoma (RB) via direct interaction with RB pocket domain

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.1311-1311

2014

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Building scenarios of digital television adoption: a pilot study

Technology analysis & strategic management, 2010-01, Vol.22 (1), p.43-63

2010

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Emotional Aspects in User Experience with Interactive Digital Television: A Case Study on Dyslexia Rehabilitation

Cross-Modal Analysis of Speech, Gestures, Gaze and Facial Expressions, p.76-89

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Erratum: Investigation of modifier genes within copy number variations in Rett syndrome

Journal of human genetics, 2012-05, Vol.57 (5), p.342-344

2012

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STEM undergraduates’ perspectives of instructor and university responses to the COVID-19 pandemic in Spring 2020

The role of institutional factors and cognitive absorption on students’ satisfaction and performance in online learning during COVID 19

Measuring student motivation on the use of a mobile assisted grammar learning tool

Predicting the intention to adopt wearable payment devices in China: The use of hybrid SEM-Neural network approach

“A friend during troubled times”: Experiences of family caregivers to persons with dementia when receiving professional support via a mobile app

User acceptance of voice biometrics in managing the physical access to a secure area of an international airport

Global profiling of alternative splicing events and gene expression regulated by hnRNPH/F

Analysis of the Phenotypes in the Rett Networked Database

Investigation of modifier genes within copy number variations in Rett syndrome

Households technology adoption and use patterns: the case of digital terrestrial television in six Italian regions

p39, the Primary Activator for Cyclin-dependent Kinase 5 (Cdk5) in Oligodendroglia, Is Essential for Oligodendroglia Differentiation and Myelin Repair

13q Deletion Syndrome Involving RB1 : Characterization of a New Minimal Critical Region for Psychomotor Delay

Ocular Surface Microbiota in Naïve Keratoconus: A Multicenter Validation Study

Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes

Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes

Ocular microbiome evaluation in dry eye disease and meibomian gland dysfunction: Values of variables

FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development

MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype

Acceptance of Information and Communication Technologies for Healthy and Active Aging: Results from Three Field Studies

AAV-mediated FOXG1 gene editing in human Rett primary cells

Low‐level TP 53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia

Abstract 1311: Notch1 inhibits retinoblastoma (RB) via direct interaction with RB pocket domain

Building scenarios of digital television adoption: a pilot study

Emotional Aspects in User Experience with Interactive Digital Television: A Case Study on Dyslexia Rehabilitation

Erratum: Investigation of modifier genes within copy number variations in Rett syndrome

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