Marcio N. Cardoso
Santo Antonio De Felheiros, Portugal
Last Updated: 09/26/2026
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Found 22 publications
Brain MRI in patients with V30M hereditary transthyretin amyloidosis.
Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: August 17, 2024
Distinct phenotypes in a cohort of anti-CASPR2 associated neurological syndromes.
Journal: Clinical neurology and neurosurgery
Published: July 09, 2023
Imaging in FIG 4-Related Parkinsonism.
Journal: Movement disorders clinical practice
Published: April 03, 2023
An SPG7 mutation as a novel cause of monogenic progressive muscular atrophy.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 15, 2023
Multisystemic RFC1-Related Disorder: Expanding the Phenotype Beyond Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome.
Journal: Neurology. Clinical practice
Published: January 05, 2023
Predictors of cognitive dysfunction in hereditary transthyretin amyloidosis with liver transplant.
Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: October 17, 2022
Corrigendum: Clinical 3-D gait assessment of patients with polyneuropathy associated with hereditary transthyretin amyloidosis.
Journal: Frontiers in neurology
Published: June 28, 2022
Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series.
Journal: Journal of clinical medicine
Published: April 20, 2022
Supporting the Assessment of Hereditary Transthyretin Amyloidosis Patients Based On 3-D Gait Analysis and Machine Learning.
Journal: IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society
Published: July 12, 2021
Clinical 3-D Gait Assessment of Patients With Polyneuropathy Associated With Hereditary Transthyretin Amyloidosis.
Journal: Frontiers in neurology
Published: September 14, 2020
Last Updated: 09/26/2026