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Cellular and molecular mechanisms of motor neuron death in amyotrophic lateral sclerosis [[electronic resource] /] / Ricardo Tapia
Cellular and molecular mechanisms of motor neuron death in amyotrophic lateral sclerosis [[electronic resource] /] / Ricardo Tapia
Autore Tapia Ricardo
Pubbl/distr/stampa Frontiers Media SA, 2015
Descrizione fisica 1 online resource (190 pages) : illustrations
Collana Frontiers Research Topics
Soggetto topico Neurology
Medicine
Health & Biological Sciences
Soggetto non controllato trophic factors
motor neuron degeneration
skeletal
neuroinflammation
muscle
genetic expression
spinal cord
amyotrophic lateral sclerosis (ALS)
ISBN 9782889193769 (ebook)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910137237503321
Tapia Ricardo  
Frontiers Media SA, 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Circuit Mechanisms of Neurodegenerative Diseases
Circuit Mechanisms of Neurodegenerative Diseases
Autore Liebscher Sabine
Pubbl/distr/stampa Frontiers Media SA, 2020
Descrizione fisica 1 electronic resource (165 p.)
Soggetto topico Science: general issues
Neurosciences
Soggetto non controllato neurodegeneration
neural circuits
Parkinson's disease
Huntington's disease
amyotrophic lateral sclerosis (ALS)
spinocerebellar ataxia (SCA)
interneurons
Alzheimer's disease
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557211003321
Liebscher Sabine  
Frontiers Media SA, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Diagnosis of neurogenetic disorders : contribution of next generation sequencing and deep phenotyping / / special issue editor, Alisdair McNeill
Diagnosis of neurogenetic disorders : contribution of next generation sequencing and deep phenotyping / / special issue editor, Alisdair McNeill
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (94 p.)
Disciplina 612.8
Soggetto topico Neurogenetics
Soggetto non controllato polymicrogyria
neurodegenerative disease
next generation sequencing (NGS)
inborn error of metabolism
genetic biomarker
deep learning
TUBA1A
Alzheimer's disease (AD)
ataxia
risk prediction
p.(Arg2His)
movement science
tubulin
R2H
diagnosis
machine learning
metal storage disorders
amyotrophic lateral sclerosis (ALS)
glucocerebrosidase
Parkinsonism
cerebellar hypoplasia
Gaucher disease
disease phenotyping
tubulinopathy
Parkinson's disease (PD)
dementia
Parkinson's disease
ISBN 3-03921-611-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Diagnosis of Neurogenetic Disorders
Record Nr. UNINA-9910367751303321
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Nerve disease ALS and gradual loss of muscle function : amytrophic lateral sclerosis / / Mary E. Miller
Nerve disease ALS and gradual loss of muscle function : amytrophic lateral sclerosis / / Mary E. Miller
Autore Miller Mary E.
Edizione [First edition.]
Pubbl/distr/stampa New York, [New York] (222 East 46th Street, New York, NY 10017) : , : Momentum Press, , 2017
Descrizione fisica 1 online resource (xiii, 39 pages) : illustrations
Disciplina 616.83
Collana Human diseases and conditions collection
Soggetto topico Amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis
Soggetto genere / forma Libros electronicos.
Soggetto non controllato amyotrophic lateral sclerosis (ALS)
Lou Gehrig's disease
motor neuron disease
neuromuscular junction
limb-onset ALS
bulbar-onset ALS
muscle weakness
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. Symptoms and diagnosis -- 2. Causes and contributing factors -- 3. Treatment and therapy -- 4. Future prospects -- Conclusion -- Bibliography -- Glossary -- About the author -- Index.
Record Nr. UNINA-9910136584103321
Miller Mary E.  
New York, [New York] (222 East 46th Street, New York, NY 10017) : , : Momentum Press, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui