Is there an axonal variety of GBS?

Early data on long-term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2-year update from the open-label extension of the NEURO-TTR trial.

European journal of neurology·2020

Does prediabetes cause small fiber sensory polyneuropathy? Does it matter?

Journal of the neurological sciences·2015

Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trials.

Journal of the neurological sciences·2014

Autonomic dysfunction in chronic inflammatory demyelinating polyradiculoneuropathy.

Neurology·2012

TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies.

Neurology·2011

Incidence and prevalence of CIDP and the association of diabetes mellitus.

Neurology·2009

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Neurology·2026

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Neurology·2026

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Neurology·2026

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Neurology·2026

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

Neurology·2026

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

Neurology·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

Is there an axonal variety of GBS?

Related Concept Videos

Early data on long-term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2-year update from the open-label extension of the NEURO-TTR trial.

Does prediabetes cause small fiber sensory polyneuropathy? Does it matter?

Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trials.

Autonomic dysfunction in chronic inflammatory demyelinating polyradiculoneuropathy.

TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies.

Incidence and prevalence of CIDP and the association of diabetes mellitus.

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

Is there an axonal variety of GBS?

Related Concept Videos

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