Paulo J. Lorenzoni

Divisão De Neurologia, Curitiba PR
Curitiba, PR, Brazil

Last Updated: 09/26/2026

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Found 73 publications

Clinical profile and quality of life in late-onset and very-late-onset myasthenia gravis: a cross-sectional study.

Clinical profile and quality of life in late-onset and very-late-onset myasthenia gravis: a cross-sectional study.

Journal: Arquivos de neuro-psiquiatria

Published: August 13, 2026

The skin-wrinkling test: principles and clinical applications.

The skin-wrinkling test: principles and clinical applications.

Journal: Arquivos de neuro-psiquiatria

Published: August 13, 2026

Prevalence and predictors of low bone mineral density in Myasthenia gravis.

Prevalence and predictors of low bone mineral density in Myasthenia gravis.

Journal: Arquivos de neuro-psiquiatria

Published: July 03, 2026

Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene.

Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene.

Journal: Journal of neurology

Published: May 02, 2026

Somatosensory Evoked Potentials in Spinocerebellar Ataxia Type 3 and Type 10.

Somatosensory Evoked Potentials in Spinocerebellar Ataxia Type 3 and Type 10.

Journal: Cerebellum (London, England)

Published: February 09, 2026

Somatosensory evoked potentials in neuromyelitis optica spectrum disorders.

Somatosensory evoked potentials in neuromyelitis optica spectrum disorders.

Journal: Neurological research

Published: January 27, 2026

Paul Hoffmann and the cutaneous silent period test.

Paul Hoffmann and the cutaneous silent period test.

Journal: Arquivos de neuro-psiquiatria

Published: June 01, 2025

Clinical and molecular characterization of limb-girdle muscular dystrophy 2G/R7 in a large cohort of Brazilian patients.

Clinical and molecular characterization of limb-girdle muscular dystrophy 2G/R7 in a large cohort of Brazilian patients.

Journal: Clinical genetics

Published: April 22, 2024

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

Showing 1-12 of 73

Last Updated: 09/26/2026