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A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V

The Journal of biological chemistry, 2001-02, Vol.276 (8), p.6009-6015

2001

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Uptake of Aβ 1–40- and Aβ 1–42-coated yeast by microglial cells: a role for LRP

Journal of leukocyte biology, 2004-08, Vol.76 (2), p.451-461

2004

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Mitochondrial respiratory chain function in skeletal muscle of ALS patients

Annals of neurology, 2002-11, Vol.52 (5), p.623-627

2002

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Pyridoxine-Induced Neuropathy in Rats: A Sensory Neuropathy That Responds to 4-Methylcatechol

Neurobiology of disease, 2001-08, Vol.8 (4), p.626-635

2001

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Possible pathogenic role of muscle cell dysfunction in motor neuron death in spinal muscular atrophy

Muscle & nerve, 2002-05, Vol.25 (5), p.700-708

2002

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Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

Muscle & nerve, 1997-01, Vol.20 (1), p.45-51

1997

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Muscle could be the therapeutic target in SMA treatment

Journal of neuroscience research, 1998-09, Vol.53 (6), p.663-669

1998

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Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron disease

Journal of neurology, 2002-03, Vol.249 (3), p.290-293

2002

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Functional maturation of nicotinic acetylcholine receptors as an indicator of murine muscular differentiation in a new nerve-muscle co-culture system

Pflügers Archiv, 2003-10, Vol.447 (1), p.14-22

2003

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Enhancement of Mouse Sciatic Nerve Regeneration by the Long Chain Fatty Alcohol,N-Hexacosanol

Experimental neurology, 1996-04, Vol.138 (2), p.189-197

1996

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Degeneration of cocultures of spinal muscular atrophy muscle cells and rat spinal cord explants is not due to secreted factors and cannot be prevented by neurotrophins

Muscle & nerve, 1997-08, Vol.20 (8), p.953-960

1997

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Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid beta peptides: their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases

Molecular medicine (Cambridge, Mass.), 1997-10, Vol.3 (10), p.695-707

1997

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Striatal dopaminergic denervation in Pallidopyramidal disease demonstrated by positron emission tomography

Annals of neurology, 1995-12, Vol.38 (6), p.954-956

1995

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Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice

Neuromuscular disorders : NMD, 2001-11, Vol.11 (8), p.722-727

2001

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The difficult-to-cultivate coxsackieviruses A can productively multiply in primary culture of mouse skeletal muscle

Virus research, 2007, Vol.123 (1), p.30-39

2007

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Cell Types Required to Efficiently Innervate Human Muscle Cells in Vitro

Experimental cell research, 2000-08, Vol.259 (1), p.204-212

2000

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Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibers in rat spinal cord-human muscle cocultures

Journal of the neurological sciences, 1996-03, Vol.136 (1), p.17-23

1996

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The frissonnant Mutant Mouse, a Model of Dopamino-Sensitive, Inherited Motor Syndrome

Neurobiology of disease, 2001-06, Vol.8 (3), p.447-458

2001

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Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system

Neuromuscular disorders : NMD, 2001-11, Vol.11 (8), p.736-746

2001

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α-Bungarotoxin sensitization in experimental autoimmune myasthenia gravis

Muscle & nerve, 1993-05, Vol.16 (5), p.461-465, Article 461

1993

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Les maladies humaines familiales à prions

Bulletin de l'Académie nationale de médecine, 2001-02, Vol.185 (2), p.405-416

Warter, Jean-Marie

2001

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Anti-titin antibodies in myasthenia gravis: tight association with thymoma and heterogeneity of nonthymoma patients

Archives of neurology (Chicago), 2001-06, Vol.58 (6), p.885

2001

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Phenotypic variability of aprataxin gene mutations

Neurology, 2003-03, Vol.60 (5), p.868-870

2003

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Construction of a Plasmid Containing Human SMN, the SMA Determining Gene, Coupled to EGFP

Plasmid, 2002-03, Vol.47 (2), p.79-87

2002

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A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V

Uptake of Aβ 1–40- and Aβ 1–42-coated yeast by microglial cells: a role for LRP

Mitochondrial respiratory chain function in skeletal muscle of ALS patients

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Pyridoxine-Induced Neuropathy in Rats: A Sensory Neuropathy That Responds to 4-Methylcatechol

Possible pathogenic role of muscle cell dysfunction in motor neuron death in spinal muscular atrophy

Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

Muscle could be the therapeutic target in SMA treatment

Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron disease

Functional maturation of nicotinic acetylcholine receptors as an indicator of murine muscular differentiation in a new nerve-muscle co-culture system

Enhancement of Mouse Sciatic Nerve Regeneration by the Long Chain Fatty Alcohol,N-Hexacosanol

Degeneration of cocultures of spinal muscular atrophy muscle cells and rat spinal cord explants is not due to secreted factors and cannot be prevented by neurotrophins

Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid beta peptides: their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases

Striatal dopaminergic denervation in Pallidopyramidal disease demonstrated by positron emission tomography

Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic mice

The difficult-to-cultivate coxsackieviruses A can productively multiply in primary culture of mouse skeletal muscle

Cell Types Required to Efficiently Innervate Human Muscle Cells in Vitro

Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibers in rat spinal cord-human muscle cocultures

The frissonnant Mutant Mouse, a Model of Dopamino-Sensitive, Inherited Motor Syndrome

Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system

α-Bungarotoxin sensitization in experimental autoimmune myasthenia gravis

Les maladies humaines familiales à prions

Anti-titin antibodies in myasthenia gravis: tight association with thymoma and heterogeneity of nonthymoma patients

Phenotypic variability of aprataxin gene mutations

Construction of a Plasmid Containing Human SMN, the SMA Determining Gene, Coupled to EGFP

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