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dc.contributor.editorFoyaca Sibat, Humberto
dc.contributor.editorde Fátima Ibañez-Valdés, Lourdes
dc.date.accessioned2021-04-20T16:15:57Z
dc.date.available2021-04-20T16:15:57Z
dc.date.issued2020
dc.identifierONIX_20210420_9781838807740_2854
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/67494
dc.description.abstractDedicated to our readers, we include novel information (not reported in IntechOpen’s books before) about new contributions of aberrant astrocytes to MND damage and death in the SOD1G93A rat experimental model of ALS; novel genetic studies on ALS; an update of the structural and functional consequences of the spinal muscular atrophy-linked mutations of the survival motor neuron protein; stem cell therapy for MND; and the novel treatment for SMA and ALS in the introductory chapter. This book contains selected peer-reviewed chapters written by international researchers. In this publication, the readers will find a compilation of state-of-the-art reviews about etiology, therapies, investigations, the molecular basis of disease progression and clinical manifestations, and the genetic familial ALS, as well as novel therapeutic modalities. We look forward with confidence and pride to the remarkable role that this book will play for a new vision and mission.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MK Medical specialties, branches of medicine::MKJ Neurology and clinical neurophysiologyen_US
dc.subject.otherNeurology & clinical neurophysiology
dc.titleNovel Aspects on Motor Neuron Disease
dc.typebook
oapen.identifier.doi10.5772/intechopen.73840
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9781838807740
oapen.relation.isbn9781838807733
oapen.relation.isbn9781838808006
oapen.imprintIntechOpen
oapen.pages118


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