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Efficacy of 30% silver diamine fluoride compared to atraumatic restorative treatment on dentine caries arrestment in primary molars of preschool children: A 12-months parallel randomized controlled clinical trial

Journal of dentistry, 2019-09, Vol.88, p.103165-103165, Article 103165

2019

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Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Neurobiology of aging, 2009-05, Vol.30 (5), p.752-758

2009

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Bra.Di.P.O. and P.I.G.R.O.: Innovative Devices for Motor Learning Programs

Journal of Robotics, 2014-01, Vol.2014 (2014), p.1-12

2014

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Vascular endothelial growth factor gene variability is associated with increased risk for AD

Annals of neurology, 2005-03, Vol.57 (3), p.373-380

2005

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P.I.G.R.O.: An Active Exoskeleton for Robotic Neurorehabilitation Training Driven by an Electro-Pneumatic Control

Advances in Service and Industrial Robotics, p.845-853

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Mitochondrial DNA G8363A mutation in the tRNA gene: Clinical, biochemical and pathological study

Journal of the neurological sciences, 2009-06, Vol.281 (1-2), p.85-92

2009

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A combined robotic and cognitive training for locomotor rehabilitation: evidences of cerebral functional reorganization in two chronic traumatic brain injured patients

Frontiers in human neuroscience, 2011-11, Vol.5, p.146-146

2011

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Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia

Journal of neurology, 2008-09, Vol.255 (9), p.1384-1391

2008

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Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis

Neurobiology of aging, 2006-05, Vol.27 (5), p.770.e1-770.e5

2006

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The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment

Journal of the neurological sciences, 2010-05, Vol.292 (1), p.107-110

2010

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The m.12316G> A mutation in the mitochondrial tRNA super(Leu(CUN)) gene is associated with mitochondrial myopathy and respiratory impairment

Journal of the neurological sciences, 2010-05, Vol.292 (1-2), p.107-110

2010

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The m.12316G>A mutation in the mitochondrial tRNALeu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment

Journal of the neurological sciences, 2010-05, Vol.292 (1), p.107-110

2010

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Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients

Neurobiology of aging, 2005-06, Vol.26 (6), p.789-794

2005

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Mitochondrial DNA G8363A mutation in the tRNA Lys gene: Clinical, biochemical and pathological study

Journal of the neurological sciences, 2009-06, Vol.281 (1), p.85-92

2009

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Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study

Journal of the neurological sciences, 2009-06, Vol.281 (1), p.85-92

2009

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PRELIMINARY STRUCTURAL ANALYSIS OF AN ACTIVE EXOSKELETON FOR ROBOTIC NEURO-REHABILITATION

International Journal of Mechatronics & Applied Mechanics, 2020-11, Vol.i (8)

2020

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Evolution of Ultrasound-Assessed Lung Aeration and Gas Exchange in Respiratory Distress Syndrome and Transient Tachypnea of the Neonate

The Journal of pediatrics, 2023-05, Vol.256, p.44-52.e2

2023

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Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis

Cell reports (Cambridge), 2019-04, Vol.27 (1), p.1-10.e4

2019

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The P2X7 Receptor Is Overexpressed in the Lesional Skin of Subjects Affected by Hidradenitis Suppurativa: A Preliminary Study

Dermatology (Basel), 2021-01, Vol.237 (1), p.111-118

2021

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Wettability of sulfonated graphene oxide membranes for proton exchange membrane fuel cells

Colloids and surfaces. A, Physicochemical and engineering aspects, 2024-03, Vol.684, p.133151, Article 133151

2024

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Less invasive surfactant administration: a word of caution

The lancet child & adolescent health, 2020-04, Vol.4 (4), p.331-340

2020

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Lactate Rewires Lipid Metabolism and Sustains a Metabolic-Epigenetic Axis in Prostate Cancer

Cancer research (Chicago, Ill.), 2022-04, Vol.82 (7), p.1267-1282

2022

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Aging in multiple sclerosis: from childhood to old age, etiopathogenesis, and unmet needs: a narrative review

Frontiers in neurology, 2023-06, Vol.14, p.1207617-1207617

2023

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The P2X7 purinergic receptor in intervertebral disc degeneration

Journal of cellular physiology, 2022-02, Vol.237 (2), p.1418-1428

2022

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Endometriosis Treatment: Role of Natural Polyphenols as Anti-Inflammatory Agents

Nutrients, 2023-06, Vol.15 (13), p.2967

2023

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Efficacy of 30% silver diamine fluoride compared to atraumatic restorative treatment on dentine caries arrestment in primary molars of preschool children: A 12-months parallel randomized controlled clinical trial

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Bra.Di.P.O. and P.I.G.R.O.: Innovative Devices for Motor Learning Programs

Vascular endothelial growth factor gene variability is associated with increased risk for AD

P.I.G.R.O.: An Active Exoskeleton for Robotic Neurorehabilitation Training Driven by an Electro-Pneumatic Control

Mitochondrial DNA G8363A mutation in the tRNA gene: Clinical, biochemical and pathological study

A combined robotic and cognitive training for locomotor rehabilitation: evidences of cerebral functional reorganization in two chronic traumatic brain injured patients

Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia

Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis

The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment

The m.12316G> A mutation in the mitochondrial tRNA super(Leu(CUN)) gene is associated with mitochondrial myopathy and respiratory impairment

The m.12316G>A mutation in the mitochondrial tRNALeu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment

Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients

Mitochondrial DNA G8363A mutation in the tRNA Lys gene: Clinical, biochemical and pathological study

Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study

PRELIMINARY STRUCTURAL ANALYSIS OF AN ACTIVE EXOSKELETON FOR ROBOTIC NEURO-REHABILITATION

Evolution of Ultrasound-Assessed Lung Aeration and Gas Exchange in Respiratory Distress Syndrome and Transient Tachypnea of the Neonate

Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis

The P2X7 Receptor Is Overexpressed in the Lesional Skin of Subjects Affected by Hidradenitis Suppurativa: A Preliminary Study

Wettability of sulfonated graphene oxide membranes for proton exchange membrane fuel cells

Less invasive surfactant administration: a word of caution

Lactate Rewires Lipid Metabolism and Sustains a Metabolic-Epigenetic Axis in Prostate Cancer

Aging in multiple sclerosis: from childhood to old age, etiopathogenesis, and unmet needs: a narrative review

The P2X7 purinergic receptor in intervertebral disc degeneration

Endometriosis Treatment: Role of Natural Polyphenols as Anti-Inflammatory Agents

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