Eva Brandao
Santa Maria Da Feira, Portugal
Last Updated: 09/26/2026
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Found 11 publications
Hereditary Spastic Paraplegia Linked to Abnormal Splicing From an AIMP1 Missense Variant.
Journal: Clinical genetics
Published: October 14, 2024
Blood neutrophils, oligoclonal bands and bridging corticosteroids as predictive factors for MOGAD course: Insights from a multicentric Portuguese cohort.
Journal: Multiple sclerosis and related disorders
Published: August 20, 2024
Determinants of age at onset in a Portuguese cohort of autosomal dominant spastic paraplegia.
Journal: Journal of the neurological sciences
Published: September 25, 2019
The epidemiology of multiple sclerosis in the entre Douro e Vouga region of northern Portugal: a multisource population-based study.
Journal: BMC neurology
Published: June 09, 2019
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Journal: American journal of human genetics
Published: March 17, 2017
Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias.
Journal: European journal of human genetics : EJHG
Published: November 23, 2016
Anterior biopercular syndrome caused by unilateral infarction.
Journal: Acta medica portuguesa
Published: February 19, 2013
Autosomal dominant spastic paraplegias: a review of 89 families resulting from a portuguese survey.
Journal: JAMA neurology
Published: February 13, 2013
Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutations.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 13, 2012
Intracerebral abscess: a rare complication of Deep Brain Stimulation.
Journal: Neurocirugia (Asturias, Spain)
Published: August 01, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026