Pablo B. Winckler

2400 Ramiro Barcelo Street
Porto Alegre, RS 90035003, Brazil

Last Updated: 09/26/2026

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Found 20 publications

Brazilian Academy of Neurology recommendations for diagnosis, management, and treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).

Brazilian Academy of Neurology recommendations for diagnosis, management, and treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).

Journal: Arquivos de neuro-psiquiatria

Published: July 28, 2025

Testing an online screening tool for epilepsy surgery evaluation.

Testing an online screening tool for epilepsy surgery evaluation.

Journal: Arquivos de neuro-psiquiatria

Published: November 12, 2024

Is late diagnosis of Duchenne muscular dystrophy still a reality?

Is late diagnosis of Duchenne muscular dystrophy still a reality?

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: September 23, 2024

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

Clinicogenetic characterization and response to disease-modifying therapies in spinal muscular atrophy: real-world experience from a reference center in Southern Brazil.

Clinicogenetic characterization and response to disease-modifying therapies in spinal muscular atrophy: real-world experience from a reference center in Southern Brazil.

Journal: Jornal de pediatria

Published: April 07, 2024

Co-Occurrence of Myotonic Dystrophy Type 1 and Limb-Girdle Muscular Dystrophy Type 2B: A Case Report.

Co-Occurrence of Myotonic Dystrophy Type 1 and Limb-Girdle Muscular Dystrophy Type 2B: A Case Report.

Journal: Molecular syndromology

Published: July 12, 2023

Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies.

Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: September 03, 2021

Evoked potentials as biomarkers of hereditary spastic paraplegias: A case-control study.

Evoked potentials as biomarkers of hereditary spastic paraplegias: A case-control study.

Journal: PloS one

Published: June 10, 2021

Speech characteristics in individuals with myasthenia gravis: a case control study.

Speech characteristics in individuals with myasthenia gravis: a case control study.

Journal: Logopedics, phoniatrics, vocology

Published: October 27, 2020

Cognitive performance in patients with Myasthenia Gravis: an association with glucocorticosteroid use and depression.

Cognitive performance in patients with Myasthenia Gravis: an association with glucocorticosteroid use and depression.

Journal: Dementia & neuropsychologia

Published: September 25, 2020

Diagnostic yield of targeted sequential and massive panel approaches for inherited neuropathies.

Diagnostic yield of targeted sequential and massive panel approaches for inherited neuropathies.

Journal: Clinical genetics

Published: March 20, 2020

Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.

Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.

Journal: Clinical genetics

Published: May 09, 2019

Showing 1-12 of 20

Last Updated: 09/26/2026