Fernando Corredor-Ortiz
Bogota, DC, Colombia
Last Updated: 09/26/2026
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Found 33 publications
Amyotrophic lateral sclerosis in Colombia: a population-based study of incidence and socioeconomic determinants.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: December 10, 2025
Perceived Impact on the Daily Lives of Patients With Spinal Muscular Atrophy Treated With Nusinersen: A Natural Language Processing Approach.
Journal: American journal of physical medicine & rehabilitation
Published: October 08, 2025
Quantitative Sensory Testing in a Girl With Tangier Disease: A Case Report.
Journal: Cureus
Published: April 03, 2025
Multimodal Evaluation of Bethlem Myopathy with the c.788G > A Variant in the COL6A1 Gene: a case report with genetic, ultrasonographic, and structural-functional discordance correlations.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: February 04, 2025
Friedreich's Ataxia in Colombia: A Population-Based Study of Incidence and Socioeconomic Determinants.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 04, 2025
Slowly progressing Amyotrophic lateral sclerosis associated with the F21L variant in the SOD1 gene: Demographic and clinical characteristics.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: October 21, 2024
Profiles of disease progression and predictors of mortality in Colombian patients with amyotrophic lateral sclerosis: a comprehensive longitudinal study.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: September 23, 2024
Small fiber neuropathy in pediatric female heterozygotes of Fabry disease: a twin case report.
Journal: BMC pediatrics
Published: September 05, 2024
Clinical and genetic characterisation of hereditary distal myopathies in a series of Colombian patients
Journal: Revista de neurologia
Published: August 29, 2024
Clinical differential factors in patients with hereditary transthyretin amyloidosis with Val142Ile and Ser43Asn mutations.
Journal: Orphanet journal of rare diseases
Published: August 04, 2024
Slowly progressive late-onset spinal muscular atrophy Finkel-type related to p.Pro56Ser VABP mutation in Colombia.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 07, 2023
Last Updated: 09/26/2026