Cecilia Martins
Vila Nova De Famalicao, Portugal
Last Updated: 09/26/2026
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Found 8 publications
Unilateral Proptosis-A Rare Presentation of Graves Disease.
Journal: Journal of paediatrics and child health
Published: November 18, 2025
Phenotypic Heterogeneity of 16p11.2 Microdeletion Syndrome: 5 Case Reports.
Journal: Journal of child neurology
Published: June 26, 2025
Pediatric Multiple Sclerosis-Experience of a Tertiary Care Center.
Journal: Neuropediatrics
Published: January 16, 2023
Pediatric neuromyelitis optica spectrum disorders in Portugal: A multicentre retrospective study.
Journal: Multiple sclerosis and related disorders
Published: December 05, 2021
Genomic imbalances defining novel intellectual disability associated loci.
Journal: Orphanet journal of rare diseases
Published: January 16, 2019
The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review.
Journal: Frontiers in genetics
Published: April 10, 2018
LEIGH SYNDROME: A CASE REPORT WITH A MITOCHONDRIAL DNA MUTATION.
Journal: Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo
Published: April 19, 2017
Risk of recurrence after a first unprovoked seizure in children.
Journal: Jornal de pediatria
Published: April 17, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026