Claudia R. Sobreira
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 12 publications
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations.
Journal: Annals of clinical and translational neurology
Published: May 22, 2024
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
Mitochondrial genome analysis in penile carcinoma.
Journal: Molecular biology reports
Published: October 27, 2017
Idiopathic hyperCKemia and malignant hyperthermia susceptibility.
Journal: Canadian journal of anaesthesia = Journal canadien d'anesthesie
Published: June 13, 2017
Reliability and validity analyses of the North Star Ambulatory Assessment in Brazilian Portuguese.
Journal: Neuromuscular disorders : NMD
Published: January 20, 2017
Guidelines for the diagnosis, treatment and clinical monitoring of patients with juvenile and adult Pompe disease.
Journal: Arquivos de neuro-psiquiatria
Published: May 12, 2015
Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy.
Journal: Brain : a journal of neurology
Published: March 22, 2015
Change in the contractile behavior of muscle fibers in subjects with primary muscle dysfunction.
Journal: NeuroRehabilitation
Published: May 08, 2013
Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course.
Journal: Journal of the neurological sciences
Published: April 10, 2008
Showing 1-12 of 12
Last Updated: 09/26/2026