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One or more keywords matched the following items that are connected to Brown, Robert
Item TypeName
Academic Article Comparison of incremental with multipoint MUNE methods in transgenic ALS mice.
Academic Article Motor unit number estimation predicts disease onset and survival in a transgenic mouse model of amyotrophic lateral sclerosis.
Academic Article Medicine. A reinnervating microRNA.
Academic Article Dysferlin overexpression in skeletal muscle produces a progressive myopathy.
Academic Article Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing.
Academic Article Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.
Academic Article Human umbilical cord blood cells differentiate into muscle in sjl muscular dystrophy mice.
Academic Article Case records of the Massachusetts General Hospital. Case 35-2006. A newborn boy with hypotonia.
Academic Article Dysferlin in membrane trafficking and patch repair.
Academic Article Arimoclomol at dosages up to 300 mg/day is well tolerated and safe in amyotrophic lateral sclerosis.
Concept Quadriceps Muscle
Concept Muscle Proteins
Concept Muscle Cramp
Concept Muscle Hypotonia
Concept Muscle Fibers, Skeletal
Concept Muscle Denervation
Concept Muscle Cells
Concept Muscle Weakness
Concept Muscle, Skeletal
Academic Article ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation.
Academic Article Natural history and biomarkers in hereditary sensory neuropathy type 1.
Academic Article A randomized trial of mexiletine in ALS: Safety and effects on muscle cramps and progression.
Academic Article A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.
Academic Article Case records of the Massachusetts General Hospital. Case 18-2006. A 57-year-old woman with numbness and weakness of the feet and legs.
Academic Article A randomized placebo-controlled phase 3 study of mesenchymal stem cells induced to secrete high levels of neurotrophic factors in amyotrophic lateral sclerosis.
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