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Early Divergence in Lymphoid Tissue Apoptosis between Pathogenic and Nonpathogenic Simian Immunodeficiency Virus Infections of Nonhuman Primates

Journal of Virology, 2008-02, Vol.82 (3), p.1175-1184

2008

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Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

Journal of neurology, 2010-05, Vol.257 (5), p.754-766

2010

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TGF-beta in intestinal lymphoid organs contributes to the death of armed effector CD8 T cells and is associated with the absence of virus containment in rhesus macaques infected with the simian immunodeficiency virus

Cell death and differentiation, 2007-10, Vol.14 (10), p.1747-1758

2007

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CD4+ CCR5+ T-Cell Dynamics during Simian Immunodeficiency Virus Infection of Chinese Rhesus Macaques

Journal of Virology, 2007-12, Vol.81 (24), p.13865-13875

2007

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New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation

Neurology, 2007-09, Vol.69 (12), p.1254-1260

2007

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Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene

Neurology, 2006-12, Vol.67 (12), p.2217-2220

2006

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Anti-dystrophin T cell responses in Duchenne muscular dystrophy: prevalence and a glucocorticoid treatment effect

Human gene therapy, 2013-09, Vol.24 (9), p.797-806

2013

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P2.4 Searching for pulmonary outcome measures in ’Early Onset’ COL6-related myopathy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.661-662

2011

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Allelic heterogeneity of SMARD1 at the IGHMBP2 locus

Human mutation, 2004-05, Vol.23 (5), p.525-526

2004

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P5.62 Garches muscle Whole-Body MRI protocol: Pattern recognition in early onset neuromuscular disorders

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.742-743

2011

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Genèse des seuils

2019

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A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36

Neurology, 2006-07, Vol.67 (1), p.120-124

2006

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P2.37 Long term prognosis of congenital myasthenic syndromes (CMS): The French CMS network experience

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.629-630

2010

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M.P.5.05 Whole-body muscle MRI in collagen type VI-related myopathies (Ullrich CMD and Bethlem myopathy)

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.628-628

2009

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EM.P.4.02 Comprehensive clinical, cellular and molecular assessment of 64 French families with COL6-related muscle disorders: Clues for genotype/phenotype correlations

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.606-607

2009

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Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases

Archives of physical medicine and rehabilitation, 2013-11, Vol.94 (11), p.2218-2226

2013

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Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association

The Journal of clinical investigation, 1996-09, Vol.98 (5), p.1130-1132

1996

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Moderate Walking Distances and Velocity Correlate with Function Comparable to 6 Minute Walk Test (S49.005)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.S49-S49.005

2012

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Functional Outcome Measures Correlated with Strength in Becker Muscular Dystrophy (P02.001)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P02-P02.001

2012

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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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Natural History of Cardiomyopathy in Duchenne Muscular Dystrophy and the Effects of Angiotensin-Converting Enzyme Inhibitor with or without -Blocker (S15.003)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.S15-S15.003

2012

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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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Identification and characterization of a spinal muscular atrophy-determining gene

Cell, 1995-01, Vol.80 (1), p.155-165

1995

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Délétion du gène SMN dans l'association arthrogrypose-amyotrophie spinale infantile

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1997, Vol.4 (9), p.908-908

1997

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Early Divergence in Lymphoid Tissue Apoptosis between Pathogenic and Nonpathogenic Simian Immunodeficiency Virus Infections of Nonhuman Primates

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

TGF-beta in intestinal lymphoid organs contributes to the death of armed effector CD8 T cells and is associated with the absence of virus containment in rhesus macaques infected with the simian immunodeficiency virus

CD4+ CCR5+ T-Cell Dynamics during Simian Immunodeficiency Virus Infection of Chinese Rhesus Macaques

New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation

Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene

Anti-dystrophin T cell responses in Duchenne muscular dystrophy: prevalence and a glucocorticoid treatment effect

P2.4 Searching for pulmonary outcome measures in ’Early Onset’ COL6-related myopathy

Les femmes et la mer à l’époque moderne

Allelic heterogeneity of SMARD1 at the IGHMBP2 locus

P5.62 Garches muscle Whole-Body MRI protocol: Pattern recognition in early onset neuromuscular disorders

Genèse des seuils

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36

P2.37 Long term prognosis of congenital myasthenic syndromes (CMS): The French CMS network experience

M.P.5.05 Whole-body muscle MRI in collagen type VI-related myopathies (Ullrich CMD and Bethlem myopathy)

EM.P.4.02 Comprehensive clinical, cellular and molecular assessment of 64 French families with COL6-related muscle disorders: Clues for genotype/phenotype correlations

Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases

Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association

Moderate Walking Distances and Velocity Correlate with Function Comparable to 6 Minute Walk Test (S49.005)

Functional Outcome Measures Correlated with Strength in Becker Muscular Dystrophy (P02.001)

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

Natural History of Cardiomyopathy in Duchenne Muscular Dystrophy and the Effects of Angiotensin-Converting Enzyme Inhibitor with or without -Blocker (S15.003)

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

Identification and characterization of a spinal muscular atrophy-determining gene

Délétion du gène SMN dans l'association arthrogrypose-amyotrophie spinale infantile

Suchergebnisse filtern