Lineu C. Werneck

Curitiba PR
Curitiba, PR, Brazil

Last Updated: 09/26/2026

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Found 75 publications

Somatosensory evoked potentials in neuromyelitis optica spectrum disorders.

Somatosensory evoked potentials in neuromyelitis optica spectrum disorders.

Journal: Neurological research
Published: January 27, 2026

A TPM2 mutation causes congenital myopathy with fibre-type disproportion.

A TPM2 mutation causes congenital myopathy with fibre-type disproportion.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 16, 2024

Myopathy due to carnitine palmitoyltransferase II deficiency: updating genetic aspects of the first publication in Brazil.

Myopathy due to carnitine palmitoyltransferase II deficiency: updating genetic aspects of the first publication in Brazil.

Journal: Arquivos de neuro-psiquiatria
Published: February 23, 2024

Triple-seronegative myasthenia gravis: clinical and epidemiological characteristics.

Triple-seronegative myasthenia gravis: clinical and epidemiological characteristics.

Journal: Arquivos de neuro-psiquiatria
Published: February 05, 2024

Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review.

Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review.

Journal: Arquivos de neuro-psiquiatria
Published: October 18, 2023

Genetic screening for transthyretin familial amyloid polyneuropathy to avoid misdiagnosis in patients with polyneuropathy associated with high protein in the cerebrospinal fluid.

Genetic screening for transthyretin familial amyloid polyneuropathy to avoid misdiagnosis in patients with polyneuropathy associated with high protein in the cerebrospinal fluid.

Journal: Acta neurologica Belgica
Published: February 02, 2023

Spectrum of SPTLC1-related disorders: a novel case of 'Ser331 syndrome' that expand the phenotype of hereditary sensory and autonomic neuropathy type 1A and motor neuron diseases.

Spectrum of SPTLC1-related disorders: a novel case of 'Ser331 syndrome' that expand the phenotype of hereditary sensory and autonomic neuropathy type 1A and motor neuron diseases.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: November 25, 2022

Visual Evoked Potentials in Neuromyelitis Optica Spectrum Disorders.

Visual Evoked Potentials in Neuromyelitis Optica Spectrum Disorders.

Journal: Journal of central nervous system disease
Published: January 07, 2022

Pain-related nociceptive evoked potential and skin wrinkle test in small fiber neuropathy.

Pain-related nociceptive evoked potential and skin wrinkle test in small fiber neuropathy.

Journal: Arquivos de neuro-psiquiatria
Published: August 11, 2021

Seventy years since the invention of the averaging technique in Neurophysiology: Tribute to George Duncan Dawson.

Seventy years since the invention of the averaging technique in Neurophysiology: Tribute to George Duncan Dawson.

Journal: Arquivos de neuro-psiquiatria
Published: July 02, 2021

Peripheral polyneuropathy from electrodiagnostic tests: a 10-year etiology and neurophysiology overview.

Peripheral polyneuropathy from electrodiagnostic tests: a 10-year etiology and neurophysiology overview.

Journal: Arquivos de neuro-psiquiatria
Published: April 20, 2021

Charcot-Marie-Tooth disease type 4C associated with myasthenia gravis: coincidental or a foreseeable association?

Charcot-Marie-Tooth disease type 4C associated with myasthenia gravis: coincidental or a foreseeable association?

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 29, 2021
Showing 1-12 of 75

Last Updated: 09/26/2026