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Guillain-Barré syndrome in SARS-CoV-2 infection: an instant systematic review of the first six months of pandemic

Journal of neurology, neurosurgery and psychiatry, 2020-10, Vol.91 (10), p.1105-1110

2020

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Autoimmune nodo-paranodopathies of peripheral nerve: the concept is gaining ground

Journal of neurology, neurosurgery and psychiatry, 2018-06, Vol.89 (6), p.627-635

2018

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New classification of autoimmune neuropathies based on target antigens and involved domains of myelinated fibres

Journal of neurology, neurosurgery and psychiatry, 2022-01, Vol.93 (1), p.57-67

2022

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Genetics of amyotrophic lateral sclerosis: A review

Journal of the neurological sciences, 2019-04, Vol.399, p.217-226

2019

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Pathology explains various mechanisms of auto‐immune inflammatory peripheral neuropathies

Brain pathology (Zurich, Switzerland), 2024-03, Vol.34 (2), p.e13184-n/a

2024

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Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology

Journal of the peripheral nervous system, 2024-06, Vol.29 (2), p.135-160

2024

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Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic and therapeutic challenges for a treatable condition

Lancet neurology, 2010-04, Vol.9 (4), p.402-412

2010

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Diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy: A "grand cru" of updated data

European journal of neurology, 2021-11, Vol.28 (11), p.3545-3546

2021

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Peripheral nerve regeneration and intraneural revascularization

Neural regeneration research, 2019-01, Vol.14 (1), p.24-33

2019

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Placebo-controlled trial of rituximab in IgM anti-myelin-associated glycoprotein neuropathy

Neurology, 2013-06, Vol.80 (24), p.2217-2225

2013

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Successful autologous hematopoietic stem cell transplantation in a refractory anti‐Caspr1 antibody nodopathy

Journal of the peripheral nervous system, 2024-03, Vol.29 (1), p.116-119

2024

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Cost of disorders of the brain in Europe 2010

European neuropsychopharmacology, 2011, Vol.21 (10), p.718-779

2011

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Hereditary neuropathies: A pathological perspective

Journal of the peripheral nervous system, 2021-11, Vol.26 (S2), p.S42-S60

2021

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Charcot–Marie–Tooth diseases: an update and some new proposals for the classification

Journal of medical genetics, 2015-10, Vol.52 (10), p.681-690

2015

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Amyloid neuropathy mimicking chronic inflammatory demyelinating polyneuropathy

Muscle & nerve, 2012-01, Vol.45 (1), p.26-31

2012

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Curcumin–cyclodextrin/cellulose nanocrystals improve the phenotype of Charcot-Marie-Tooth-1A transgenic rats through the reduction of oxidative stress

Free radical biology & medicine, 2020-12, Vol.161, p.246-262

2020

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Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update

Journal of the neurological sciences, 2014-12, Vol.347 (1), p.14-22

2014

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Epidemics and outbreaks of peripheral nervous system disorders: II. Toxic and nutritional causes

Journal of neurology, 2021-03, Vol.268 (3), p.892-902

2021

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Ultrastructural Lesions of Nodo-Paranodopathies in Peripheral Neuropathies

Journal of neuropathology and experimental neurology, 2020-03, Vol.79 (3), p.247-255

2020

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Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes

Journal of neurology, 2021-03, Vol.268 (3), p.879-890

2021

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Peripheral Nerve Disorders: Pathology and Genetics

1st edition., 2014

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Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation

eLife, 2023-04, Vol.12

2023

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Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport

Brain pathology (Zurich, Switzerland), 2017-07, Vol.27 (4), p.459-471

2017

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Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy

American journal of human genetics, 2013-02, Vol.92 (2), p.271-278

2013

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Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes

Journal of the peripheral nervous system, 2013-06, Vol.18 (2), p.113-129

2013

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Guillain-Barré syndrome in SARS-CoV-2 infection: an instant systematic review of the first six months of pandemic

Autoimmune nodo-paranodopathies of peripheral nerve: the concept is gaining ground

New classification of autoimmune neuropathies based on target antigens and involved domains of myelinated fibres

Genetics of amyotrophic lateral sclerosis: A review

Pathology explains various mechanisms of auto‐immune inflammatory peripheral neuropathies

Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology

Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic and therapeutic challenges for a treatable condition

Diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy: A "grand cru" of updated data

Peripheral nerve regeneration and intraneural revascularization

Placebo-controlled trial of rituximab in IgM anti-myelin-associated glycoprotein neuropathy

Successful autologous hematopoietic stem cell transplantation in a refractory anti‐Caspr1 antibody nodopathy

Cost of disorders of the brain in Europe 2010

Hereditary neuropathies: A pathological perspective

Charcot–Marie–Tooth diseases: an update and some new proposals for the classification

Amyloid neuropathy mimicking chronic inflammatory demyelinating polyneuropathy

Curcumin–cyclodextrin/cellulose nanocrystals improve the phenotype of Charcot-Marie-Tooth-1A transgenic rats through the reduction of oxidative stress

Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update

Epidemics and outbreaks of peripheral nervous system disorders: II. Toxic and nutritional causes

Ultrastructural Lesions of Nodo-Paranodopathies in Peripheral Neuropathies

Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes

Peripheral Nerve Disorders: Pathology and Genetics

Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation

Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport

Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy

Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes

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