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motor neuron disease
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Motor neuron disease
2010 |
Central Library of Charles University
publication
Motor neuron disease
2010 |
Faculty of Medicine in Pilsen
publication
An unusual case of progressive supranuclear ophtalmoplegia accompanied by motor neuron disease
2008 |
Faculty of Arts
publication
Motor neuron disease and chorea
Publication without faculty affiliation
publication
Palliative care in terminal states of motor neuron diseases (amyotrophic lateral sclerosis, progressive bulbar palsy, and progressive muscular atrophy)
+1
2010 |
Second Faculty of Medicine
publication
FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases
2011 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Humanities
publication
Structure of cognitive deficit in amyotrophic lateral sclerosis
Publication without faculty affiliation
publication
Diagnostic utility of neurofilament markers for MND is limited in restricted disease phenotype and for differentiation from compressive myeloradiculopathies
2023 |
Central Library of Charles University, Second Faculty of Medicine
publication
Voice disorder as a symptom of amyotrophic lateral sclerosis
2021 |
Faculty of Medicine in Hradec Králové
publication
Neurodegenerative disorders
2014 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Selective vulnerability of motor neuron types and functional groups to degeneration in amyotrophic lateral sclerosis: review of the neurobiological mechanisms and functional correlates
2024 |
Central Library of Charles University, Third Faculty of Medicine
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A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity
2020 |
Central Library of Charles University
publication
Molecular pathology of ALS: What we currently know and what important information is still missing
2021 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Structure of cognitive deficit in amyotrophic lateral sclerosis
2007 |
Faculty of Arts
publication
Use of functional electrical stimulation in adult neurological patients: how it can be used to manage gait issues
2020 |
First Faculty of Medicine
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Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease
2022 |
First Faculty of Medicine
publication
Pathophysiology of ion channels in amyotrophic lateral sclerosis
2023 |
Third Faculty of Medicine
publication
Current Concepts in the Classification and Diagnosis of Frontotemporal Lobar Degenerations A Practical Approach
2014 |
Third Faculty of Medicine
publication
New insights in the diagnosis and treatment of amyotrophic lateral sclerosis
2018 |
Central Library of Charles University, Third Faculty of Medicine
publication
Neurodegenerative disorders
2019 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration
2012 |
Second Faculty of Medicine
publication
Role of Oxidative Stress in the Pathogenesis of Amyotrophic Lateral Sclerosis: Antioxidant Metalloenzymes and Therapeutic Strategies
2021 |
Faculty of Medicine in Hradec Králové
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Hereditary motor neuropathies
2016 |
Second Faculty of Medicine
publication
Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients
2017 |
Second Faculty of Medicine
publication
Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found
2020 |
Second Faculty of Medicine
publication
Relationship between ALS and the degree of cognitive impairment, markers of neurodegeneration and predictors for poor outcome: A prospective study
2010 |
Central Library of Charles University, First Faculty of Medicine, Third Faculty of Medicine, Faculty of Arts
publication
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study
2008 |
Second Faculty of Medicine
publication
Clinical neuropsychology in practice
+1
2017 |
Faculty of Arts