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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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Multi-grams scale purification of xanthanolides from Xanthium macrocarpum: Centrifugal partition chromatography versus silica gel chromatography

Journal of chromatography, 2007-06, Vol.1151 (1-2), p.14-19

2007

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Impact of hospital infection on medical expenditures in a continuing care and rehabilitation service at a geriatric hospital

Pathologie biologie (Paris), 1998-06, Vol.46 (6), p.398-402

1998

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Pathogenesis of miners' nystagmus

Minerva medica, 1950-03, Vol.41 (15), p.505

AUDO-GIANOTTI, G B

1950

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Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms

Progress in retinal and eye research, 2015-03, Vol.45, p.58-110

2015

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Multiplex PCR for detection of seven virulence factors and K1/K2 capsular serotypes of Klebsiella pneumoniae

Journal of clinical microbiology, 2014-12, Vol.52 (12), p.4377-4380

2014

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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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Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9)

JAMA ophthalmology, 2017-11, Vol.135 (11), p.1232

2017

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Considerations on the pathogenesis of tumors in professionals

Minerva medica, 1949-09, Vol.40 (46 Pt 2), p.357

AUDO-GIANOTTI, G B

1949

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EARLY DIAGNOSIS OF MALIGNANT BLOOD DISEASES

Il Cancro, 1963, Vol.16, p.64

AUDO-GIANOTTI, G B

1963

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Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients With Stargardt Disease: SMART Study Report No. 2

American journal of ophthalmology, 2022-04, Vol.236, p.32-44

2022

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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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Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium

Investigative ophthalmology & visual science, 2015-02, Vol.56 (2), p.918-931

2015

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Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration

American journal of ophthalmology, 2023-08, Vol.252, p.77-93

2023

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Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17)

American journal of ophthalmology, 2023-06, Vol.250, p.157-170

2023

Volltextzugriff (PDF)

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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Baseline Microperimetry and OCT in the RUSH2A Study: Structure−Function Association and Correlation With Disease Severity

American journal of ophthalmology, 2022-12, Vol.244, p.98-116

2022

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The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene

Investigative ophthalmology & visual science, 2022-03, Vol.63 (3), p.17-17

2022

Volltextzugriff (PDF)

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

American journal of human genetics, 2013-01, Vol.92 (1), p.67-75

2013

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Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation

Human mutation, 2020-01, Vol.41 (1), p.255-264

2020

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Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene

Human mutation, 2019-08, Vol.40 (8), p.1145-1155, Article humu.23768

2019

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A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness

American journal of human genetics, 2010-10, Vol.87 (4), p.523-531

2010

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The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy

Proceedings of the National Academy of Sciences - PNAS, 2022-07, Vol.119 (27), p.e2115538119

2022

Volltextzugriff (PDF)

Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity

Acta ophthalmologica (Oxford, England), 2023-03, Vol.101 (2), p.e261-e263

2023

Volltextzugriff (PDF)

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

Multi-grams scale purification of xanthanolides from Xanthium macrocarpum: Centrifugal partition chromatography versus silica gel chromatography

Impact of hospital infection on medical expenditures in a continuing care and rehabilitation service at a geriatric hospital

Pathogenesis of miners' nystagmus

Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms

Multiplex PCR for detection of seven virulence factors and K1/K2 capsular serotypes of Klebsiella pneumoniae

Gut-derived acetate promotes B10 cells with antiinflammatory effects

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

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9)

Considerations on the pathogenesis of tumors in professionals

EARLY DIAGNOSIS OF MALIGNANT BLOOD DISEASES

Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients With Stargardt Disease: SMART Study Report No. 2

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

Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium

Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration

Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17)

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

Baseline Microperimetry and OCT in the RUSH2A Study: Structure−Function Association and Correlation With Disease Severity

The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation

Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene

A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness

The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy

Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity

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