About: Neuromuscular

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Attributs	Valeurs
type	Concept
rdfs:label	Neuromuscular
skos:inScheme	http://hub.abes.fr/referentiel/bmjarticlecategories
is Subject of	Changes in quality of life scores with intravenous immunoglobulin or plasmapheresis in patients with myasthenia gravis Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1 Clinical features of CIDP with LM1-associated antibodies Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations Pathophysiology of HNPP explored using axonal excitability Lifetime physical activity and the risk of amyotrophic lateral sclerosis Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophy Antibodies against the main immunogenic region of the acetylcholine receptor correlate with disease severity in myasthenia gravis The spectrum of immune-mediated autonomic neuropathies: insights from the clinicopathological features Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B Comprehensive analysis of the TRPV4 gene in a large series of inherited neuropathies and controls Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features Biology of the blood-nerve barrier and its alteration in immune mediated neuropathies Bickerstaff brainstem encephalitis and Fisher syndrome: anti-GQ1b antibody syndrome Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing Non-demyelinating, reversible conduction failure in Fisher syndrome and related disorders Outcome and its predictors in Guillain-Barré syndrome Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2 Chronic inflammatory demyelinating polyradiculoneuropathy in solid organ transplant recipients: a prospective study Overlooked non-motor symptoms in myasthenia gravis Evidence of multidimensionality in the ALSFRS-R Scale: a critical appraisal on its measurement properties using Rasch analysis Ambiguous effects of anti-VEGF monoclonal antibody (bevacizumab) for POEMS syndrome Serum IgG levels in IV immunoglobulin treated chronic inflammatory demyelinating polyneuropathy

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