Ines C. Carrilho
Santo Antonio De Felheiros, Portugal
Last Updated: 09/26/2026
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Found 14 publications
Expanding the ATP2B3 Phenotype: Progressive Dystonia and Basal Ganglia Atrophy.
Journal: Pediatric neurology
Published: April 06, 2026
Tongue tremor in a paediatric patient with essential tremor.
Journal: BMJ case reports
Published: February 12, 2025
Recurrent Encephalopathy as a Form of Presentation of Transport Protein Particle Complex 11-Related Disease: A Family Matter.
Journal: Pediatric neurology
Published: June 03, 2024
Familial occipital lobe epilepsy associated with GABAA receptor variants.
Journal: Seizure
Published: June 13, 2023
Primary headache with onset in childhood and adolescence: natural history and prognostic factors in a Portuguese population.
Journal: Revista de neurologia
Published: December 22, 2022
Congenital ataxia due to novel variant in ATP8A2.
Journal: Clinical genetics
Published: January 16, 2021
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.
Journal: Neurology
Published: December 23, 2019
A rare early-onset dystonia (DYT16) in a Portuguese girl
Journal: Revista de neurologia
Published: June 14, 2018
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Journal: Brain : a journal of neurology
Published: November 03, 2014
The expanding clinical and genetic spectrum of ATP1A3-related disorders.
Journal: Neurology
Published: February 14, 2014
Chronic inflammatory demyelinating polyneuropathy associated with autoimmune hepatitis.
Journal: Pediatric neurology
Published: January 24, 2014
Tuberous sclerosis: clinical characteristics and their relationship to genotype/phenotype
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: September 17, 2013
Last Updated: 09/26/2026