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Can mortality data be used to estimate amyotrophic lateral sclerosis incidence?
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Alteration of nutritional status at diagnosis is a prognostic factor for surv...
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Lead exposure stimulates VEGF expression in the spinal cord and extends survi...
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Extracellular ATP and the P2X7 receptor in astrocyte-mediated motor neuron de...
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Phenotypically aberrant astrocytes that promote motoneuron damage in a model ...
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Modulation of astrocytic mitochondrial function by dichloroacetate improves s...
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Muscle gene expression is a marker of amyotrophic lateral sclerosis severity.
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Juvenile and adult-onset ALS/MND among Africans: incidence, phenotype, surviv...
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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP ...
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[SLA, cognition and clinical practice].
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Mutations of the ANG gene in French patients with sporadic amyotrophic latera...
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Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ...
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FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral s...
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The P413L chromogranin B variation in French patients with sporadic amyotroph...
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Association between divalent metal transport 1 encoding gene (SLC11A2) and di...
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amy...
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Study of the HFE gene common polymorphisms in French patients with sporadic a...
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Trauma and amyotrophic lateral sclerosis: a case-control study from a populat...
International audience
