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Neurological manifestations of primary Sjogren's syndrome

Current opinion in neurology, 2010-10, Vol.23 (5), p.509-513

2010

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The diagnosis and treatment of myotonic disorders

Muscle & nerve, 2013-05, Vol.47 (5), p.632-648

2013

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Acute nutritional axonal neuropathy

Muscle & nerve, 2018-01, Vol.57 (1), p.33-39

2018

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Clinical Spectrum and Prognosis in Patients With Acute Nutritional Axonal Neuropathy

Neurology, 2023-05, Vol.100 (20), p.e2134

2023

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Positive paraneoplastic panels: Probabilities, perils, and pearls

Muscle & nerve, 2022-05, Vol.65 (5), p.489-491

2022

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Dispersion of the distal compound muscle action potential as a diagnostic criterion for chronic inflammatory demyelinating polyneuropathy

Neurology, 2002-11, Vol.59 (10), p.1526-1532

2002

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Neurological manifestations of primary Sjogren's syndrome

Current opinion in neurology, 2010-10, Vol.23 (5), p.509

2010

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Electrodiagnosis of Myotonic Disorders

Physical medicine and rehabilitation clinics of North America, 2013-02, Vol.24 (1), p.209-220

2013

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Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy

Muscle & nerve, 2007-04, Vol.35 (4), p.479-485

2007

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The prognosis of electrodiagnosis

Muscle & nerve, 2018-08, Vol.58 (2), p.178-181

2018

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Neuropathy due to coexistent vitamin B12 and B6 deficiencies in patients with Parkinson's disease: A case series

Journal of the neurological sciences, 2021-11, Vol.430, p.120028-120028, Article 120028

2021

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Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome

Neurology, 2015-12, Vol.85 (22), p.1964-1971

2015

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Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1)

Muscle & nerve, 2007-09, Vol.36 (3), p.320-328

2007

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Amplitude-dependent slowing of conduction in amyotrophic lateral sclerosis and polyneuropathy

Muscle & nerve, 1999-07, Vol.22 (7), p.937-940

1999

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Long Exercise Test in Periodic Paralysis: A Bayesian Analysis

Muscle & nerve, 2019-01, Vol.59 (1), p.47-54

2019

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Acute inflammatory demyelinating polyneuropathy: Contribution of a dispersed distal compound muscle action potential to electrodiagnosis

Muscle & nerve, 2006-06, Vol.33 (6), p.771-777

2006

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Successful Treatment of Lyme Encephalopathy with Intravenous Ceftriaxone

The Journal of infectious diseases, 1999-08, Vol.180 (2), p.377-383

1999

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Visualization of the diaphragm muscle with ultrasound improves diagnostic accuracy of phrenic nerve conduction studies

Muscle & nerve, 2014-05, Vol.49 (5), p.669-675

2014

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Dispersion of compound muscle action potential in hereditary neuropathies and chronic inflammatory demyelinating polyneuropathy

Muscle & nerve, 2006-10, Vol.34 (4), p.417-422

2006

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Clinical Evaluation of Membrane Excitability in Muscle Channel Disorders: Potential Applications in Clinical Trials

Neurotherapeutics, 2007-04, Vol.4 (2), p.205-215

2007

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Acute and chronic pain associated with Lyme borreliosis: Clinical characteristics and pathophysiologic mechanisms

Pain (Amsterdam), 2014-08, Vol.155 (8), p.1435-1438

2014

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Rapid resolution of severe neuralgic amyotrophy after treatment with corticosteroids and intravenous immunoglobulin

Muscle & nerve, 2011-08, Vol.44 (2), p.304-305

2011

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Pediatric CIDP: Clinical Features and Response to Treatment

Journal of clinical neuromuscular disease, 2017-12, Vol.19 (2), p.57-65

2017

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Electrodiagnosis of ulnar neuropathy at the elbow (Une): A bayesian approach

Muscle & nerve, 2014-03, Vol.49 (3), p.337-344

2014

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Class of nerve fiber involvement in sensory neuropathies: Clinical characterization and utility of the plantar nerve action potential

Muscle & nerve, 2002-08, Vol.26 (2), p.212-217

2002

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Neurological manifestations of primary Sjogren's syndrome

The diagnosis and treatment of myotonic disorders

Acute nutritional axonal neuropathy

Clinical Spectrum and Prognosis in Patients With Acute Nutritional Axonal Neuropathy

Positive paraneoplastic panels: Probabilities, perils, and pearls

Dispersion of the distal compound muscle action potential as a diagnostic criterion for chronic inflammatory demyelinating polyneuropathy

Neurological manifestations of primary Sjogren's syndrome

Electrodiagnosis of Myotonic Disorders

Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy

The prognosis of electrodiagnosis

Neuropathy due to coexistent vitamin B12 and B6 deficiencies in patients with Parkinson's disease: A case series

Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome

Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1)

Amplitude-dependent slowing of conduction in amyotrophic lateral sclerosis and polyneuropathy

Long Exercise Test in Periodic Paralysis: A Bayesian Analysis

Acute inflammatory demyelinating polyneuropathy: Contribution of a dispersed distal compound muscle action potential to electrodiagnosis

Successful Treatment of Lyme Encephalopathy with Intravenous Ceftriaxone

Visualization of the diaphragm muscle with ultrasound improves diagnostic accuracy of phrenic nerve conduction studies

Dispersion of compound muscle action potential in hereditary neuropathies and chronic inflammatory demyelinating polyneuropathy

Clinical Evaluation of Membrane Excitability in Muscle Channel Disorders: Potential Applications in Clinical Trials

Acute and chronic pain associated with Lyme borreliosis: Clinical characteristics and pathophysiologic mechanisms

Rapid resolution of severe neuralgic amyotrophy after treatment with corticosteroids and intravenous immunoglobulin

Pediatric CIDP: Clinical Features and Response to Treatment

Electrodiagnosis of ulnar neuropathy at the elbow (Une): A bayesian approach

Class of nerve fiber involvement in sensory neuropathies: Clinical characterization and utility of the plantar nerve action potential

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