Reinaldo I. Takata
Av. Amazonas, 5953
Belo Horizonte, MG 30510000, Brazil
Belo Horizonte, MG 30510000, Brazil
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 14 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
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCs.
Journal: Disease models & mechanisms
Published: July 17, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability.
Journal: Journal of molecular neuroscience : MN
Published: February 15, 2019
Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas.
Journal: Molecular genetics & genomic medicine
Published: June 30, 2017
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
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).
Journal: Metallomics : integrated biometal science
Published: June 14, 2016
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Journal: Arquivos de neuro-psiquiatria
Published: March 12, 2014
Last Updated: 09/26/2026