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Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy

Brain (London, England : 1878), 2017-07, Vol.140 (7), p.1851-1858

2017

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Sural-sparing is seen in axonal as well as demyelinating forms of Guillain–Barré syndrome

Clinical neurophysiology, 2015-12, Vol.126 (12), p.2376-2380

2015

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Nodal proteins are target antigens in Guillain-Barré syndrome

Journal of the peripheral nervous system, 2012-03, Vol.17 (1), p.62-71

2012

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Acute painful autoimmune neuropathy: A variant of Guillain‐Barré syndrome

Muscle & nerve, 2018-02, Vol.57 (2), p.320-324

2018

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Two sets of nerve conduction studies may suffice in reaching a reliable electrodiagnosis in Guillain–Barré syndrome

Clinical neurophysiology, 2013-07, Vol.124 (7), p.1456-1459

2013

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Epidemiology of Campylobacter jejuni Isolated from Patients with Guillain-Barré and Fisher Syndromes in Japan

Journal of Clinical Microbiology, 2005, Vol.43 (1), p.335-339

2005

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Reversible conduction failure is distinct from neurophysiological patterns of recovery in mild demyelinating Guillain–Barré syndrome

Journal of the neurological sciences, 2013-03, Vol.326 (1), p.111-114

2013

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Bickerstaff brainstem encephalitis and Fisher syndrome: anti-GQ1b antibody syndrome

Journal of Neurology, Neurosurgery and Psychiatry, 2013-05, Vol.84 (5), p.576-583

2013

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Proteinuria is a key to suspect autoimmune nodopathies

European journal of neurology, 2024-10, Vol.31 (10), p.e16406-n/a

2024

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Subclass IgG to motor gangliosides related to infection and clinical course in Guillain–Barré syndrome

Journal of neuroimmunology, 2008-02, Vol.194 (1), p.181-190

2008

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Neurofascin-155 IgG4 in chronic inflammatory demyelinating polyneuropathy

Neurology, 2016-03, Vol.86 (9), p.800-807

2016

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Patients with chronic inflammatory demyelinating polyneuropathy initially diagnosed as Guillain-Barré syndrome

Journal of neurology, 2003-08, Vol.250 (8), p.913-916

2003

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Differences in membrane properties of axonal and demyelinating Guillain-Barré syndromes

Annals of neurology, 2002-08, Vol.52 (2), p.180-187

2002

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Clinical correlates of serum anti-GT1a IgG antibodies

Journal of the neurological sciences, 2004-04, Vol.219 (1), p.139-145

2004

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Contactin 1 IgG4 associates to chronic inflammatory demyelinating polyneuropathy with sensory ataxia

Brain (London, England : 1878), 2015-06, Vol.138 (Pt 6), p.1484-1491

2015

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Continuous spectrum of pharyngeal-cervical-brachial variant of Guillain-Barré syndrome

Archives of neurology (Chicago), 2007-10, Vol.64 (10), p.1519

2007

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Sialylated IgG-Fc: a novel biomarker of chronic inflammatory demyelinating polyneuropathy

Journal of neurology, neurosurgery and psychiatry, 2016-03, Vol.87 (3), p.275-279

2016

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Polyneuritis cranialis: oculopharyngeal subtype of Guillain-Barré syndrome

Journal of Neurology, 2015-09, Vol.262 (9), p.2001-2012

2015

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A Guillain-Barré syndrome variant with prominent facial diplegia

Journal of neurology, 2009-11, Vol.256 (11), p.1899-1905

2009

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Non-demyelinating, reversible conduction failure in Fisher syndrome and related disorders

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (9), p.941-948

2012

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Delayed facial palsy in Miller Fisher syndrome

Journal of the neurological sciences, 2015-11, Vol.358 (1), p.409-412

2015

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Guillain–Barré syndrome associated with normal or exaggerated tendon reflexes

Journal of neurology, 2012-06, Vol.259 (6), p.1181-1190

2012

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Recurrent Guillain–Barré syndrome, Miller Fisher syndrome and Bickerstaff brainstem encephalitis

Journal of the neurological sciences, 2016-05, Vol.364, p.59-64

2016

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Serial peripheral nerve ultrasound in Guillain–Barré syndrome

Clinical neurophysiology, 2016-02, Vol.127 (2), p.1652-1656

2016

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The demyelination neurophysiological criteria can be misleading in Campylobacter jejuni -related Guillain–Barré syndrome

Clinical neurophysiology, 2013-08, Vol.124 (8), p.1671-1679

2013

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Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy

Sural-sparing is seen in axonal as well as demyelinating forms of Guillain–Barré syndrome

Nodal proteins are target antigens in Guillain-Barré syndrome

Acute painful autoimmune neuropathy: A variant of Guillain‐Barré syndrome

Two sets of nerve conduction studies may suffice in reaching a reliable electrodiagnosis in Guillain–Barré syndrome

Epidemiology of Campylobacter jejuni Isolated from Patients with Guillain-Barré and Fisher Syndromes in Japan

Reversible conduction failure is distinct from neurophysiological patterns of recovery in mild demyelinating Guillain–Barré syndrome

Bickerstaff brainstem encephalitis and Fisher syndrome: anti-GQ1b antibody syndrome

Proteinuria is a key to suspect autoimmune nodopathies

Subclass IgG to motor gangliosides related to infection and clinical course in Guillain–Barré syndrome

Neurofascin-155 IgG4 in chronic inflammatory demyelinating polyneuropathy

Patients with chronic inflammatory demyelinating polyneuropathy initially diagnosed as Guillain-Barré syndrome

Differences in membrane properties of axonal and demyelinating Guillain-Barré syndromes

Clinical correlates of serum anti-GT1a IgG antibodies

Contactin 1 IgG4 associates to chronic inflammatory demyelinating polyneuropathy with sensory ataxia

Continuous spectrum of pharyngeal-cervical-brachial variant of Guillain-Barré syndrome

Sialylated IgG-Fc: a novel biomarker of chronic inflammatory demyelinating polyneuropathy

Polyneuritis cranialis: oculopharyngeal subtype of Guillain-Barré syndrome

A Guillain-Barré syndrome variant with prominent facial diplegia

Non-demyelinating, reversible conduction failure in Fisher syndrome and related disorders

Delayed facial palsy in Miller Fisher syndrome

Guillain–Barré syndrome associated with normal or exaggerated tendon reflexes

Recurrent Guillain–Barré syndrome, Miller Fisher syndrome and Bickerstaff brainstem encephalitis

Serial peripheral nerve ultrasound in Guillain–Barré syndrome

The demyelination neurophysiological criteria can be misleading in Campylobacter jejuni -related Guillain–Barré syndrome

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