Neurophysiological features of primary lateral sclerosis

Neurophysiological features of primary lateral sclerosis

Primary lateral sclerosis (PLS) is a motor neuron disease characterized by spinobulbar spasticity, absence of progressive lower motor neuron (LMN) dysfunction and marked by a slow functional decline. Electromyography is essential to exclude significant LMN involvement, particularly in the context of...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	de Carvalho, M, Kiernan, MC, Pullman, SL, Rezenia, K, Turner, M, Simmons, Z
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	Taylor and Francis 2021

Παρόμοια τεκμήρια

Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis.
ανά: Hudson, A, κ.ά.
Έκδοση: (1993)

Kinnier Wilson's puzzling features of amyotrophic lateral sclerosis
ανά: Turner, MR, κ.ά.
Έκδοση: (2017)

Biomarkers in amyotrophic lateral sclerosis.
ανά: Turner, M, κ.ά.
Έκδοση: (2009)

Primary lateral sclerosis: consensus diagnostic criteria
ανά: Turner, MR, κ.ά.
Έκδοση: (2020)

Neurophysiological testing in the diagnosis of amyotrophic lateral sclerosis
ανά: David Burke
Έκδοση: (2022-01-01)

Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria.
ανά: Pringle, C, κ.ά.
Έκδοση: (1992)

Clinical characteristics and neurophysiology features of amyotrophic lateral sclerosis patients at Sanglah Hospital Denpasar
ανά: I Made Odie Lastrawan, κ.ά.
Έκδοση: (2021-09-01)

Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?
ανά: Turner, M, κ.ά.
Έκδοση: (2012)

Amyotrophic lateral sclerosis.
ανά: Kiernan, M, κ.ά.
Έκδοση: (2011)

Primary lateral sclerosis: diagnosis and management
ανά: Turner, MR, κ.ά.
Έκδοση: (2020)

Occasional essay: Upper motor neuron syndrome in amyotrophic lateral sclerosis
ανά: Swash, M, κ.ά.
Έκδοση: (2020)

Neuroimaging in primary lateral sclerosis
ανά: Pioro, EP, κ.ά.
Έκδοση: (2021)

Neurophysiological Differences between Flail Arm Syndrome and Amyotrophic Lateral Sclerosis.
ανά: Hecheng Yang, κ.ά.
Έκδοση: (2015-01-01)

Regional callosal integrity and bilaterality of limb weakness in amyotrophic lateral sclerosis
ανά: Tu, S, κ.ά.
Έκδοση: (2020)

Assessment of the upper motor neuron in amyotrophic lateral sclerosis
ανά: Huynh, W, κ.ά.
Έκδοση: (2016)

Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
ανά: Henderson, R, κ.ά.
Έκδοση: (2018)

Myelin imaging in amyotrophic and primary lateral sclerosis.
ανά: Kolind, S, κ.ά.
Έκδοση: (2013)

Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis
ανά: Liu-Qing Xu, κ.ά.
Έκδοση: (2020-10-01)

Mechanisms, models and biomarkers in amyotrophic lateral sclerosis.
ανά: Turner, M, κ.ά.
Έκδοση: (2013)

Quantifying disease progression in amyotrophic lateral sclerosis.
ανά: Simon, N, κ.ά.
Έκδοση: (2014)

The clinical spectrum of primary lateral sclerosis
ανά: Barohn, R, κ.ά.
Έκδοση: (2021)

Functional Biomarkers for Amyotrophic Lateral Sclerosis
ανά: William Huynh, κ.ά.
Έκδοση: (2019-01-01)

Neurophysiological Mechanisms Underlying Cortical Hyper-Excitability in Amyotrophic Lateral Sclerosis: A Review
ανά: Jonu Pradhan, κ.ά.
Έκδοση: (2021-04-01)

Amyotrophic lateral sclerosis in Slovenia – analysis of patient population at the Ljubljana Institute of Clinical Neurophysiology
ανά: Mojca Kirbiš, κ.ά.
Έκδοση: (2015-09-01)

The standard of care in amyotrophic lateral sclerosis: a centralised multidisciplinary clinic encounter sets a new benchmark for a uniquely challenging neurodegenerative disorder.
ανά: Turner, M, κ.ά.
Έκδοση: (2014)

Regional thalamic MRI as a marker of widespread cortical pathology and progressive frontotemporal involvement in amyotrophic lateral sclerosis
ανά: Tu, S, κ.ά.
Έκδοση: (2018)

Neurophysiological indices for split phenomena: correlation with age and sex and potential implications in amyotrophic lateral sclerosis
ανά: Stefano Zoccolella, κ.ά.
Έκδοση: (2024-03-01)

Controversies and priorities in amyotrophic lateral sclerosis.
ανά: Turner, M, κ.ά.
Έκδοση: (2013)

The reunification of amyotrophic lateral sclerosis
ανά: Turner, M
Έκδοση: (2018)

Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis.
ανά: Filippini, N, κ.ά.
Έκδοση: (2010)

The Neonatal Microbiome: Implications for Amyotrophic Lateral Sclerosis and Other Neurodegenerations
ανά: Andrew Eisen, κ.ά.
Έκδοση: (2025-02-01)

Comment on: Teaching Neuroimages: Hypometabolism of the primary motor cortex in primary lateral sclerosis: The stripe sign.
ανά: Turner, M, κ.ά.
Έκδοση: (2016)

The importance of neurophysiological-Bobath method in multiple sclerosis
ανά: Adrian Miler, κ.ά.
Έκδοση: (2018-02-01)

The importance of neurophysiological-Bobath method in multiple sclerosis
ανά: Adrian Miler, κ.ά.
Έκδοση: (2018-02-01)

Sweet food preference in amyotrophic lateral sclerosis
ανά: Turner, M, κ.ά.
Έκδοση: (2017)

What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?
ανά: Hogden A, κ.ά.
Έκδοση: (2013-02-01)

Regional motor cortex dysfunction in amyotrophic lateral sclerosis
ανά: Parvathi Menon, κ.ά.
Έκδοση: (2019-08-01)

Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study
ανά: Peter Bede, κ.ά.
Έκδοση: (2019-01-01)

Multi-component relaxation reveals distinct patterns of white matter involvement in primary progressive multiple sclerosis and primary lateral sclerosis
ανά: Kolind, S, κ.ά.
Έκδοση: (2012)

Imaging Findings Associated with Cognitive Performance in Primary Lateral Sclerosis and Amyotrophic Lateral Sclerosis
ανά: Avner Meoded, κ.ά.
Έκδοση: (2013-08-01)