Antonio R. Neto-Coimbra
Campinas, SP, Brazil
Last Updated: 09/26/2026
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Found 8 publications
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Journal: The Journal of clinical investigation
Published: July 08, 2024
Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy.
Journal: Arquivos de neuro-psiquiatria
Published: March 14, 2023
Intrafamilial phenotypic heterogeneity related to a new DMD splice site variant.
Journal: Neuromuscular disorders : NMD
Published: August 16, 2020
A Novel Multisystem Proteinopathy Caused by a Missense ANXA11 Variant.
Journal: Annals of neurology
Published: April 24, 2020
Characterisation of ataxia in Sjogren's syndrome.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: November 04, 2019
Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.
Journal: Clinical genetics
Published: May 09, 2019
Clinical and molecular findings in a cohort of ANO5-related myopathy.
Journal: Annals of clinical and translational neurology
Published: March 11, 2019
Male systemic lupus erythematosus, an overlooked diagnosis.
Journal: Clinics and practice
Published: September 28, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026