Excitability of sensory axons in amyotrophic lateral sclerosis

[1]  V. Marchand-Pauvert,et al.  Abnormal cortical brain integration of somatosensory afferents in ALS , 2017, Clinical Neurophysiology.

[2]  A. Fuglsang-Frederiksen,et al.  Reproducibility, and sensitivity to motor unit loss in amyotrophic lateral sclerosis, of a novel MUNE method: MScanFit MUNE , 2017, Clinical Neurophysiology.

[3]  M. Swash,et al.  Fasciculation in amyotrophic lateral sclerosis: origin and pathophysiological relevance , 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

[4]  E. Hedlund,et al.  Motor neuron vulnerability and resistance in amyotrophic lateral sclerosis , 2017, Acta Neuropathologica.

[5]  J. Jakobsen,et al.  Quantitative sensory testing and structural assessment of sensory nerve fibres in amyotrophic lateral sclerosis , 2017, Journal of the Neurological Sciences.

[6]  C. Lin,et al.  Uncovering sensory axonal dysfunction in asymptomatic type 2 diabetic neuropathy , 2017, PloS one.

[7]  G. Mora,et al.  Non‐motor involvement in amyotrophic lateral sclerosis: new insight from nerve and vessel analysis in skin biopsy , 2017, Neuropathology and applied neurobiology.

[8]  N. Wray,et al.  Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity , 2017, Expert review of neurotherapeutics.

[9]  A. Fuglsang-Frederiksen,et al.  Involvement of distal sensory nerves in amyotrophic lateral sclerosis , 2016, Muscle & nerve.

[10]  A. Al-Chalabi,et al.  Amyotrophic lateral sclerosis: moving towards a new classification system , 2016, The Lancet Neurology.

[11]  A. Fuglsang-Frederiksen,et al.  Laser and somatosensory evoked potentials in amyotrophic lateral sclerosis , 2016, Clinical Neurophysiology.

[12]  G. Lauria,et al.  Mutant SOD1 accumulation in sensory neurons does not associate with endoplasmic reticulum stress features: Implications for differential vulnerability of sensory and motor neurons to SOD1 toxicity , 2016, Neuroscience Letters.

[13]  C. Krarup,et al.  Estimating motor unit numbers from a CMAP scan , 2016, Muscle & nerve.

[14]  X. Navarro,et al.  Involvement of sensory innervation in the skin of SOD1G93A ALS mice , 2016, Journal of the peripheral nervous system : JPNS.

[15]  C. Gellera,et al.  Amyotrophic lateral sclerosis causes small fiber pathology , 2016, European journal of neurology.

[16]  C. Desnuelle,et al.  Deciphering spreading mechanisms in amyotrophic lateral sclerosis: clinical evidence and potential molecular processes. , 2015, Current opinion in neurology.

[17]  K. Byth,et al.  Rate of disease progression: a prognostic biomarker in ALS , 2015, Journal of Neurology, Neurosurgery & Psychiatry.

[18]  M. Swash,et al.  The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odyssey , 2015, Journal of Neurology, Neurosurgery & Psychiatry.

[19]  H. Benali,et al.  Electrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosis , 2015, BMJ Open.

[20]  Matthew C Kiernan,et al.  Quantifying Disease Progression in Amyotrophic Lateral Sclerosis , 2014, Annals of neurology.

[21]  J. Rothstein,et al.  Advances in treating amyotrophic lateral sclerosis: insights from pathophysiological studies , 2014, Trends in Neurosciences.

[22]  M. Kiernan,et al.  Riluzole exerts central and peripheral modulating effects in amyotrophic lateral sclerosis. , 2013, Brain : a journal of neurology.

[23]  M. Swash,et al.  Controversies and priorities in amyotrophic lateral sclerosis , 2013, The Lancet Neurology.

[24]  S. Rossignol,et al.  Involvement of spinal sensory pathway in ALS and specificity of cord atrophy to lower motor neuron degeneration , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

[25]  David Burke,et al.  The voltage dependence of Ih in human myelinated axons , 2012, The Journal of physiology.

[26]  Toshio Shimizu,et al.  Proportional neuronal loss between the primary motor and sensory cortex in amyotrophic lateral sclerosis , 2011, Neuroscience Letters.

[27]  O. Hardiman,et al.  Amyotrophic lateral sclerosis , 2011, The Lancet.

[28]  K. Asanuma,et al.  Utility of recovery cycle with two conditioning pulses for detection of impaired axonal slow potassium current in ALS , 2010, Clinical Neurophysiology.

[29]  Niels Birbaumer,et al.  Neuroimaging of multimodal sensory stimulation in amyotrophic lateral sclerosis , 2010, Journal of Neurology, Neurosurgery & Psychiatry.

[30]  Michael O'Brien,et al.  Aids to the examination of the peripheral nervous system: 6th edition , 2023, Practical Neurology.

[31]  D. Burke,et al.  In vivo assessment of HCN channel current (Ih) in human motor axons , 2010, Muscle & nerve.

[32]  C. Krarup,et al.  Nerve conduction and excitability studies in peripheral nerve disorders , 2009, Current opinion in neurology.

[33]  Shu-Yu Wu,et al.  Sensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis , 2009, Experimental & Molecular Medicine.

[34]  Bernardo Lanzillo,et al.  Sensory deficit in Parkinson's disease: evidence of a cutaneous denervation. , 2008, Brain : a journal of neurology.

[35]  M. Swash,et al.  Electrodiagnostic criteria for diagnosis of ALS , 2008, Clinical Neurophysiology.

[36]  J. Glass,et al.  Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS , 2007, Neurology.

[37]  Ammar Al-Chalabi,et al.  Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder? , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[38]  M. de Carvalho,et al.  Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[39]  Matthew C. Kiernan,et al.  Axonal excitability properties in amyotrophic lateral sclerosis , 2006, Clinical Neurophysiology.

[40]  Kazuaki Kanai,et al.  Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage. , 2006, Brain : a journal of neurology.

[41]  M. Benatar,et al.  Sural and radial sensory responses in healthy adults: Diagnostic implications for polyneuropathy , 2005, Muscle & nerve.

[42]  R. Stein,et al.  The resilience of the size principle in the organization of motor unit properties in normal and reinnervated adult skeletal muscles. , 2004, Canadian journal of physiology and pharmacology.

[43]  D. Burke,et al.  Differences in responses of cutaneous afferents in the human median and sural nerves to ischemia , 2001, Muscle & nerve.

[44]  D. Burke,et al.  Excitability of human axons , 2001, Clinical Neurophysiology.

[45]  N. Murray,et al.  Clinical evaluation of excitability measures in sensory nerve , 2001, Muscle & nerve.

[46]  H Bostock,et al.  Effects of temperature on the excitability properties of human motor axons. , 2001, Brain : a journal of neurology.

[47]  D. Burke,et al.  Accommodation to depolarizing and hyperpolarizing currents in cutaneous afferents of the human median and sural nerves , 2000, The Journal of physiology.

[48]  D. Burke,et al.  Recovery of excitability of cutaneous afferents in the median and sural nerves following activity , 2000, Muscle & nerve.

[49]  D. Burke,et al.  Multiple measures of axonal excitability: A new approach in clinical testing , 2000, Muscle & nerve.

[50]  J. Cedarbaum,et al.  The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function , 1999, Journal of the Neurological Sciences.

[51]  D Burke,et al.  Temperature dependence of excitability indices of human cutaneous afferents , 1999, Muscle & nerve.

[52]  D. Burke,et al.  Ischemic resistance of cutaneous afferents and motor axons in patients with amyotrophic lateral sclerosis , 1998, Muscle & nerve.

[53]  D. Burke,et al.  Strength-duration properties of sensory and motor axons in amyotrophic lateral sclerosis. , 1998, Brain : a journal of neurology.

[54]  D. Burke,et al.  Threshold tracking techniques in the study of human peripheral nerve , 1998, Muscle & nerve.

[55]  J. Slade,et al.  Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changes , 1996, Acta Neuropathologica.

[56]  D Burke,et al.  Strength-duration properties of human peripheral nerve. , 1996, Brain : a journal of neurology.

[57]  Michael Donaghy,et al.  Progressive sensory nerve dysfunction in amyotrophic lateral sclerosis: a prospective clinical and neurophysiological study , 1993, Journal of Neurology.

[58]  A. Rossi,et al.  Involvement of peripheral sensory fibers in amyotrophic lateral sclerosis: Electro‐physiological study of 64 cases , 1993, Muscle & nerve.

[59]  R. Radtke,et al.  Abnormal sensory evoked potentials in amyotrophic lateral sclerosis , 1986, Neurology.

[60]  G. Jamal,et al.  Sensory involvement in motor neuron disease: further evidence from automated thermal threshold determination. , 1985, Journal of neurology, neurosurgery, and psychiatry.

[61]  P. Dyck,et al.  Morphometric Comparison of the Vulnerability of Peripheral Motor and Sensory Neurons in Amyotrophic Lateral Sclerosis , 1981, Journal of neuropathology and experimental neurology.

[62]  D. Burke,et al.  Sensory conduction of the sural nerve in polyneuropathy1 , 1974, Journal of neurology, neurosurgery, and psychiatry.

[63]  Jun Kimura,et al.  Electrodiagnosis in Diseases of Nerve and Muscle , 2013 .

[64]  R. Kaji,et al.  Physiology and pathophysiology of myelinated nerve fibers. , 2013, Handbook of clinical neurology.

[65]  K. Takahashi,et al.  Familial amyotrophic lateral sclerosis: Features of multisystem degeneration , 2004, Acta Neuropathologica.

[66]  S. Allpress,et al.  Sensory nerve pathology in amyotrophic lateral sclerosis , 2004, Acta Neuropathologica.