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Extinction ratio enhancement by sinusoidal phase modulation and nonlinear spectral focusing

Laser physics, 2017-11, Vol.27 (11), p.115401

2017

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Raman amplification in an optically high-powered data link dedicated to a 10 km long extension for submarine cabled observatories

Journal of optics (2010), 2013-05, Vol.15 (5), p.55703-1-8

2013

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Study of the optical phenomena in a 10 km long optically powered data link dedicated to a submarine cabled observatory

2013 MTS/IEEE OCEANS - Bergen, 2013, p.1-9

2013

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Gut-derived acetate promotes B10 cells with antiinflammatory effects

JCI insight, 2021-04, Vol.6 (7)

2021

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The Negative ERG: Clinical Phenotypes and Disease Mechanisms of Inner Retinal Dysfunction

Survey of ophthalmology, 2008-01, Vol.53 (1), p.16-40

2008

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Adult-onset foveomacular vitelliform dystrophy: A fresh perspective

Progress in retinal and eye research, 2015-07, Vol.47, p.64-85

2015

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RNA-based therapies in inherited retinal diseases

Therapeutic Advances in Ophthalmology, 2022-01, Vol.14, p.251584142211346-25158414221134602

2022

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Orthogonal Analysis Underscores the Relevance of Primary and Secondary Metabolites in Licorice

Journal of natural products (Washington, D.C.), 2014-08, Vol.77 (8), p.1806-1816

2014

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Distinct Effects of Soluble and Membrane‐Bound Fas Ligand on Fibroblast‐like Synoviocytes From Rheumatoid Arthritis Patients

Arthritis & rheumatology (Hoboken, N.J.), 2014-12, Vol.66 (12), p.3289-3299

2014

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Venous thromboembolism in critically ill patients affected by ARDS related to COVID-19 in Northern-West Italy

European review for medical and pharmacological sciences, 2020-09, Vol.24 (17), p.9154

2020

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Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy

Scientific reports, 2021-08, Vol.11 (1), p.16412-16412, Article 16412

2021

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Real-World Safety and Effectiveness of Voretigene Neparvovec: Results up to 2 Years from the Prospective, Registry-Based PERCEIVE Study

Biomolecules (Basel, Switzerland), 2024-01, Vol.14 (1), p.122

2024

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Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue

npj Regenerative medicine, 2022-08, Vol.7 (1), p.39-39, Article 39

2022

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Rapid linear scale-up of a protein separation by centrifugal partition chromatography

Journal of Chromatography A, 2008-05, Vol.1190 (1), p.57-62

2008

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Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity

American journal of ophthalmology, 2020-11, Vol.219, p.87-100

2020

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Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors

Investigative ophthalmology & visual science, 2020-09, Vol.61 (11), p.18-18

2020

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A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific reports, 2020-01, Vol.10 (1), p.1584-1584, Article 1584

2020

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Retinal degeneration in mucopolysaccharidose type II

Graefe's archive for clinical and experimental ophthalmology, 2013-07, Vol.251 (7), p.1871-1872

2013

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ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant

Clinical genetics, 2017-07, Vol.92 (1), p.109-111

2017

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Non-infarctual ST elevation and acute cardiopulmonary failure in carbon monoxide poisoning: a case report

European review for medical and pharmacological sciences, 2019-08, Vol.23 (16), p.7128

2019

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A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed research international, 2018-01, Vol.2018, p.7694801-10

2018

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Update on recommendations for screening for hydroxychloroquine retinopathy

Journal francais d'ophtalmologie, 2017-11, Vol.40 (9), p.793

2017

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

American journal of human genetics, 2012-02, Vol.90 (2), p.321-330

2012

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Extinction ratio enhancement by sinusoidal phase modulation and nonlinear spectral focusing

Raman amplification in an optically high-powered data link dedicated to a 10 km long extension for submarine cabled observatories

Study of the optical phenomena in a 10 km long optically powered data link dedicated to a submarine cabled observatory

Gut-derived acetate promotes B10 cells with antiinflammatory effects

The Negative ERG: Clinical Phenotypes and Disease Mechanisms of Inner Retinal Dysfunction

Adult-onset foveomacular vitelliform dystrophy: A fresh perspective

RNA-based therapies in inherited retinal diseases

Orthogonal Analysis Underscores the Relevance of Primary and Secondary Metabolites in Licorice

Distinct Effects of Soluble and Membrane‐Bound Fas Ligand on Fibroblast‐like Synoviocytes From Rheumatoid Arthritis Patients

Venous thromboembolism in critically ill patients affected by ARDS related to COVID-19 in Northern-West Italy

Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy

Real-World Safety and Effectiveness of Voretigene Neparvovec: Results up to 2 Years from the Prospective, Registry-Based PERCEIVE Study

Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue

Rapid linear scale-up of a protein separation by centrifugal partition chromatography

Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Retinal degeneration in mucopolysaccharidose type II

ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant

Non-infarctual ST elevation and acute cardiopulmonary failure in carbon monoxide poisoning: a case report

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

Update on recommendations for screening for hydroxychloroquine retinopathy

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries. An International Survey by the European Vision Institute

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