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Modeling and pathophysiological analysis of the ubiquilin-2-linked amyotrophic lateral sclerosis (ALS) with AAV vectors

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S225-S225

2015

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G.O.20

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.921-921

2014

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Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase

Science translational medicine, 2017-11, Vol.9 (418)

2017

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P3.10 Intramuscular AAV9 administration enables transgene delivery to motor neurons in the whole spinal cord: Therapeutic application in a SMA mouse model

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.685-685

2011

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O.18 Intravenous injection of SMN1-expressing self-complementary AAV9 rescues severe type I SMA mice

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.640-640

2010

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Adenovirus in the brain: recent advances of gene therapy for neurodegenerative diseases

Progress in neurobiology, 1998-07, Vol.55 (4), p.333-341

1998

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AAV9-mediated SMN expression restricted to the CNS does not rescue SMA mice

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S136

2017

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P.132 - AAV9-mediated SMN expression restricted to the CNS does not rescue SMA mice

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S136-S136

2017

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Implication of the SMN complex in the biogenesis and steady state level of the signal recognition particle

Nucleic acids research, 2013-01, Vol.41 (2), p.1255-1272

2013

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Role of muscle satellite cells in Spinal muscular atrophy physiopathology

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S136

2017

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P.131 - Role of muscle satellite cells in Spinal muscular atrophy physiopathology

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S136-S136

2017

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Synaptic Sprouting Increases the Uptake Capacities of Motoneurons in Amyotrophic Lateral Sclerosis Mice

Proceedings of the National Academy of Sciences - PNAS, 2001-06, Vol.98 (13), p.7582-7587

2001

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G.P.133 - Modeling and pathophysiological analysis of the ubiquilin-2-linked amyotrophic lateral sclerosis (ALS) with AAV vectors

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S225-S225

2015

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G.O.4 The NF-kappaB activator PLEKHG5 gene is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.767-767

2007

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TH.O.16 - A new AAV10-mediated gene therapy for SOD1-linked ALS

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S246-S246

2017

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A new AAV10-mediated gene therapy for SOD1 -linked ALS

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S246

2017

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The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

American journal of human genetics, 2007-07, Vol.81 (1), p.67-76

2007

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TH.O.17 - Whole-body rescue of Pompe disease with AAV liver delivery of engineered secretable GAA transgenes

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S246-S246

2017

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Whole-body rescue of Pompe disease with AAV liver delivery of engineered secretable GAA transgenes

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S246

2017

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G.O.20: AAV-mediated overexpression of Ubiquilin2 mimics ALS and ALS with dementia in naive mice

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.921-921

2014

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Effects of Ginkgo biloba extract (EGb 761) on learning and possible actions on aging

Journal of physiology, Paris, 1997-12, Vol.91 (6), p.291-300

1997

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Intrastriatal grafts of embryonic mesencephalic rat neurons genetically modified using an adenovirus encoding human Cu/Zn superoxide dismutase

Neuroscience, 1997-06, Vol.78 (3), p.703-713

1997

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Vulnerable newborn types: analysis of subnational, population-based birth cohorts for 541 285 live births in 23 countries, 2000-2021

BJOG : an international journal of obstetrics and gynaecology, 2023-05

2023

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1-methyl-4-phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase

Journal of neuroscience research, 2006-02, Vol.83 (2), p.233-242

2006

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Combining Fractal Coding and Orthogonal Linear Transforms

ISRN signal processing, 2011, Vol.2011 (2011), p.1-9

2011

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Modeling and pathophysiological analysis of the ubiquilin-2-linked amyotrophic lateral sclerosis (ALS) with AAV vectors

G.O.20

Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase

P3.10 Intramuscular AAV9 administration enables transgene delivery to motor neurons in the whole spinal cord: Therapeutic application in a SMA mouse model

O.18 Intravenous injection of SMN1-expressing self-complementary AAV9 rescues severe type I SMA mice

Adenovirus in the brain: recent advances of gene therapy for neurodegenerative diseases

AAV9-mediated SMN expression restricted to the CNS does not rescue SMA mice

P.132 - AAV9-mediated SMN expression restricted to the CNS does not rescue SMA mice

Implication of the SMN complex in the biogenesis and steady state level of the signal recognition particle

Role of muscle satellite cells in Spinal muscular atrophy physiopathology

P.131 - Role of muscle satellite cells in Spinal muscular atrophy physiopathology

Synaptic Sprouting Increases the Uptake Capacities of Motoneurons in Amyotrophic Lateral Sclerosis Mice

G.P.133 - Modeling and pathophysiological analysis of the ubiquilin-2-linked amyotrophic lateral sclerosis (ALS) with AAV vectors

G.O.4 The NF-kappaB activator PLEKHG5 gene is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset

TH.O.16 - A new AAV10-mediated gene therapy for SOD1-linked ALS

A new AAV10-mediated gene therapy for SOD1 -linked ALS

The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

TH.O.17 - Whole-body rescue of Pompe disease with AAV liver delivery of engineered secretable GAA transgenes

Whole-body rescue of Pompe disease with AAV liver delivery of engineered secretable GAA transgenes

G.O.20: AAV-mediated overexpression of Ubiquilin2 mimics ALS and ALS with dementia in naive mice

Effects of Ginkgo biloba extract (EGb 761) on learning and possible actions on aging

Intrastriatal grafts of embryonic mesencephalic rat neurons genetically modified using an adenovirus encoding human Cu/Zn superoxide dismutase

Vulnerable newborn types: analysis of subnational, population-based birth cohorts for 541 285 live births in 23 countries, 2000-2021

1-methyl-4-phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase

Combining Fractal Coding and Orthogonal Linear Transforms

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