Literature DB >> 28674982

Motoneuron Disease: Clinical.

Hristelina Ilieva1, Nicholas J Maragakis2.   

Abstract

ALS is a neurodegenerative disease in which the primary symptoms result in progressive neuromuscular weakness. Recent studies have highlighted that there is significant heterogeneity with regard to anatomical and temporal disease progression. Importantly, more recent advances in genetics have revealed new causative genes to the disease. New efforts have focused on the development of biomarkers that could aid in diagnosis, prognosis, and serve as pharmacodynamics markers. Although traditional pharmaceuticals continue to undergo trials for ALS, new therapeutic strategies including stem cell transplantation studies, gene therapies, and antisense therapies targeting some of the familial forms of ALS are gaining momentum.

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Keywords:  Diagnosis; Exercise; Frontotemporal dementia; Gene therapy; Heterogeneity; Nutrition; Phenotype; Respiratory management; Stem cell therapy

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Year:  2017        PMID: 28674982     DOI: 10.1007/978-3-319-57193-5_7

Source DB:  PubMed          Journal:  Adv Neurobiol


  1 in total

1.  Neuroprotective effects of violacein in a model of inherited amyotrophic lateral sclerosis.

Authors:  Silvia Olivera-Bravo; Carmen Bolatto; Gabriel Otero Damianovich; Matías Stancov; Sofía Cerri; Paola Rodríguez; Daniela Boragno; Karina Hernández Mir; María Noel Cuitiño; Fernanda Larrambembere; Eugenia Isasi; Diego Alem; Lucía Canclini; Marta Marco; Danilo Davyt; Pablo Díaz-Amarilla
Journal:  Sci Rep       Date:  2022-03-15       Impact factor: 4.379

  1 in total

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