Jaquelin Valicek
Av. Amazonas, 5953
Belo Horizonte, MG 30510000, Brazil
Belo Horizonte, MG 30510000, Brazil
Last Updated: 09/26/2026
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Found 11 publications
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms.
Journal: Genes
Published: March 23, 2022
Muscle fat replacement and modified ragged red fibers in two patients with reversible infantile respiratory chain deficiency.
Journal: Neuromuscular disorders : NMD
Published: September 24, 2020
Clinical, imaging, morphologic, and molecular features of X-linked VMA21-related myopathy in two unrelated Brazilian families.
Journal: Journal of the neurological sciences
Published: April 24, 2020
Early-onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic COQ8A variants, including a large intragenic deletion.
Journal: JIMD reports
Published: December 24, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability.
Journal: Journal of molecular neuroscience : MN
Published: February 15, 2019
Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: February 10, 2017
The relative frequency of common neuromuscular diagnoses in a reference center.
Journal: Arquivos de neuro-psiquiatria
Published: August 08, 2016
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Journal: Arquivos de neuro-psiquiatria
Published: March 12, 2014
Muscle phenotypic variability in limb girdle muscular dystrophy 2 G.
Journal: Journal of molecular neuroscience : MN
Published: February 04, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026