Decoding Amyotrophic Lateral Sclerosis: Discovery of Novel Disease-Related Biomarkers and Future Perspectives in Neurodegeneration
Resumen: Amyotrophic lateral sclerosis (ALS) belongs to the group of motor neuron diseases, in which the degeneration, the weakness of voluntary muscles, and death of motor neurons gradually spread along disease progression. ALS comes
from Greek language and means “no muscle nourishment” (“amyotrophic”), “area of the spinal cord where affected nerve cells are localized” (“lateral”), and “the degeneration and hardening of the spinal cord” (“sclerosis”). The fundamental contributions of the celebrated neurologist Jean-Martin Charcot at the end of the nineteenth century provided the first description of ALS....

Idioma: Inglés
DOI: 10.1155/2014/629630
Año: 2014
Publicado en: BioMed Research International 2014 (2014), 629630 [2 pp]
ISSN: 2314-6133

Factor impacto JCR: 1.579 (2014)
Categ. JCR: MEDICINE, RESEARCH & EXPERIMENTAL rank: 85 / 123 = 0.691 (2014) - Q3 - T3
Categ. JCR: BIOTECHNOLOGY & APPLIED MICROBIOLOGY rank: 107 / 163 = 0.656 (2014) - Q3 - T2

Tipo y forma: (Published version)
Área (Departamento): Área Genética (Dpto. Anatom.,Embri.Genét.Ani.)

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Exportado de SIDERAL (2020-10-23-13:53:17)

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