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Systematic Review and Meta‐Analysis of Diagnostic Accuracy of Serum Refractometry and Brix Refractometry for the Diagnosis of Inadequate Transfer of Passive Immunity in Calves

Journal of veterinary internal medicine, 2018-01, Vol.32 (1), p.474-483

2018

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Coupling powder bed additive manufacturing and vapor phase deposition methods for elaboration of coated 3D Ti-6Al-4V architectures with enhanced surface properties

Surface & coatings technology, 2021-06, Vol.415, p.127130, Article 127130

2021

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Muscle‐specific, liver‐detargeted adeno‐associated virus gene therapy rescues Pompe phenotype in adult and neonate Gaa−/− mice

Journal of inherited metabolic disease, 2024-01, Vol.47 (1), p.119-134

2024

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Impact of conservation measures on demography and genetic variability of livestock breeds

Animal (Cambridge, England), 2020-04, Vol.14 (4), p.670-680

2020

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G.P.279

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.901-901

2014

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Structure, Rheological Behavior, and in Situ Local Flow Fields of Cellulose Nanocrystal Dispersions during Cross-Flow Ultrafiltration

ACS sustainable chemistry & engineering, 2019-06, Vol.7 (12), p.10679-10689

2019

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P58 WITHDRAWN Cardiomyocyte death after AAV gene transfer can be related to proteotoxicity or to transgene abnormal function or localization

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S73

2023

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LGMD AUTOSOMAL RESSESSIVE AND DOMINANT: P.98AAV-mediated gene transfer of FKRP for therapy of LGMD2I

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S59-S59

2018

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LGMD AUTOSOMAL RESSESSIVE AND DOMINANT

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S59

2018

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G.O.3 A human skeletal muscle interactome centered on proteins involved in muscular dystrophies

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.873-873

2012

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G.P.279: Efficient AAV-mediated transfer of FKRP in a new mouse model of Limb Girdle Muscular Dystrophy 2I

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.901-901

2014

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37P TreatMYPN: In vivo mouse characterization and in vitro 3D muscle studies followed by 15P AAV gene therapy for the ultrarare myopalladin-related congenital myopathy

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.235

2024

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Microphotonics for monitoring the supramolecular thermoresponsive behavior of fatty acid surfactant solutions

Optics communications, 2020-08, Vol.468, p.125773, Article 125773

2020

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Adeno-associated virus pseudotype 5 vector improves gene transfer in arthritic joints

Human gene therapy, 2005-04, Vol.16 (4), p.426-434

2005

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PRE-CLINICAL DEVELOPMENTS IN NEUROMUSCULAR DISORDERS

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S161-S162

2021

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PRE-CLINICAL DEVELOPMENTS IN NEUROMUSCULAR DISORDERS: O.15 Unprecedented low dose of AAV-mediated gene transfer corrects the pathology in a model for Fukutin-related-protein deficiencies

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S161-S162

2021

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DMD – ANIMAL MODELS: EP.93 The DLK1-DIO3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in DMD

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S77-S77

2021

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DMD – ANIMAL MODELS

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S77

2021

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Establishment of a panel for the evaluation of the dystrophic process by quantitative RT-PCR

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S166

2017

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P.236 - Establishment of a panel for the evaluation of the dystrophic process by quantitative RT-PCR

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S166-S166

2017

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G.P.8.12 Mannosidase I inhibition rescues the human α -sarcoglycan R77C recurrent mutation

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.785-785

2008

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Safety and Efficacy of AAV-Mediated Calpain 3 Gene Transfer in a Mouse Model of Limb-Girdle Muscular Dystrophy Type 2A

Molecular therapy, 2006-02, Vol.13 (2), p.250-259

2006

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Investigation of the Positive Response of Ethyl Acrylate in the Mouse Lymphoma Genotoxicity Assay

Toxicological sciences, 1998-12, Vol.46 (2), p.324-332

1998

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Adduct formation by photo-induced electron transfer between photo-oxidising Ru(II) complexes and tryptophan

Chemical communications (Cambridge, England), 2004-12 (23), p.2764-2765

2004

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Photoelectron transfer processes with ruthenium (II) polypyridyl complexes and Cu/Zn superoxide dismutase

Biochemistry (Easton), 2006 (45)

2006

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Systematic Review and Meta‐Analysis of Diagnostic Accuracy of Serum Refractometry and Brix Refractometry for the Diagnosis of Inadequate Transfer of Passive Immunity in Calves

Coupling powder bed additive manufacturing and vapor phase deposition methods for elaboration of coated 3D Ti-6Al-4V architectures with enhanced surface properties

Muscle‐specific, liver‐detargeted adeno‐associated virus gene therapy rescues Pompe phenotype in adult and neonate Gaa−/− mice

Impact of conservation measures on demography and genetic variability of livestock breeds

G.P.279

Structure, Rheological Behavior, and in Situ Local Flow Fields of Cellulose Nanocrystal Dispersions during Cross-Flow Ultrafiltration

P58 WITHDRAWN Cardiomyocyte death after AAV gene transfer can be related to proteotoxicity or to transgene abnormal function or localization

LGMD AUTOSOMAL RESSESSIVE AND DOMINANT: P.98AAV-mediated gene transfer of FKRP for therapy of LGMD2I

LGMD AUTOSOMAL RESSESSIVE AND DOMINANT

G.O.3 A human skeletal muscle interactome centered on proteins involved in muscular dystrophies

G.P.279: Efficient AAV-mediated transfer of FKRP in a new mouse model of Limb Girdle Muscular Dystrophy 2I

37P TreatMYPN: In vivo mouse characterization and in vitro 3D muscle studies followed by 15P AAV gene therapy for the ultrarare myopalladin-related congenital myopathy

Microphotonics for monitoring the supramolecular thermoresponsive behavior of fatty acid surfactant solutions

Adeno-associated virus pseudotype 5 vector improves gene transfer in arthritic joints

PRE-CLINICAL DEVELOPMENTS IN NEUROMUSCULAR DISORDERS

PRE-CLINICAL DEVELOPMENTS IN NEUROMUSCULAR DISORDERS: O.15 Unprecedented low dose of AAV-mediated gene transfer corrects the pathology in a model for Fukutin-related-protein deficiencies

DMD – ANIMAL MODELS: EP.93 The DLK1-DIO3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in DMD

DMD – ANIMAL MODELS

Establishment of a panel for the evaluation of the dystrophic process by quantitative RT-PCR

P.236 - Establishment of a panel for the evaluation of the dystrophic process by quantitative RT-PCR

G.P.8.12 Mannosidase I inhibition rescues the human α -sarcoglycan R77C recurrent mutation

Safety and Efficacy of AAV-Mediated Calpain 3 Gene Transfer in a Mouse Model of Limb-Girdle Muscular Dystrophy Type 2A

Investigation of the Positive Response of Ethyl Acrylate in the Mouse Lymphoma Genotoxicity Assay

Adduct formation by photo-induced electron transfer between photo-oxidising Ru(II) complexes and tryptophan

Photoelectron transfer processes with ruthenium (II) polypyridyl complexes and Cu/Zn superoxide dismutase

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