Ana R. Goncalves
Porto, Portugal
Last Updated: 09/26/2026
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Found 27 publications
A new case of platelet-type von Willebrand disease supports the recent findings of gain-of-function GP1BA variants outside the C-terminal disulphide loop enhances affinity for von Willebrand factor.
Journal: British journal of haematology
Published: April 28, 2023
Predictors of cognitive dysfunction one-year post COVID-19.
Journal: Neuropsychology
Published: January 05, 2023
Thrombocytopenia-Absent Radius Syndrome: Descriptions of Three New Cases and a Novel Splicing Variant in RBM8A That Expands the Spectrum of Null Alleles.
Journal: International journal of molecular sciences
Published: August 05, 2022
Effects of Concomitant Benzodiazepines and Antidepressants Long-Term Use on Social Decision-Making: Results From the Ultimatum Game.
Journal: Frontiers in psychology
Published: April 07, 2022
Effects of aging on face processing: An ERP study of the own-age bias with neutral and emotional faces.
Journal: Cortex; a journal devoted to the study of the nervous system and behavior
Published: March 31, 2022
Awareness to utilitarian responses in later life: An ERP study with moral dilemmas.
Journal: Neuroscience letters
Published: January 12, 2022
Integrating Whole-Genome Sequencing in Clinical Genetics: A Novel Disruptive Structural Rearrangement Identified in the Dystrophin Gene (DMD).
Journal: International journal of molecular sciences
Published: November 27, 2021
CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in RASGRP2.
Journal: International journal of molecular sciences
Published: October 01, 2021
Would surgical Apgar score be useful to predict postoperative complications after proximal femoral fracture surgery? - A retrospective cohort study.
Journal: Revista espanola de anestesiologia y reanimacion
Published: June 07, 2021
Central Pain in Parkinson's Disease: Behavioral and Cognitive Characteristics.
Journal: Parkinson's disease
Published: February 10, 2021
X-Linked Myotubular Myopathy: A Novel Mutation Expanding the Genotypic Spectrum of a Phenotypically Heterogeneous Myopathy.
Journal: Journal of pediatric genetics
Published: December 13, 2020
Last Updated: 09/26/2026