Andressa B. Glaeser
Porto Alegre, RS, Brazil
Last Updated: 09/26/2026
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Found 12 publications
Hospital characteristics associated with COVID-19 mortality: data from the multicenter cohort Brazilian Registry.
Journal: Internal and emergency medicine
Published: April 01, 2022
Longer length of stay, days between discharge/first readmission, and pulmonary involvement ≥50% increase prevalence of admissions in ICU in unplanned readmissions after COVID-19 hospitalizations.
Journal: Journal of medical virology
Published: December 16, 2021
22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders.
Journal: Molecular syndromology
Published: December 02, 2021
ABC2-SPH risk score for in-hospital mortality in COVID-19 patients: development, external validation and comparison with other available scores.
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
Published: June 11, 2021
Congenital Heart Defects and 22q11.2 Deletion Syndrome: A 20-Year Update and New Insights to Aid Clinical Diagnosis.
Journal: Journal of pediatric genetics
Published: April 30, 2021
A child with cat-eye syndrome and oculo-auriculo-vertebral spectrum phenotype: A discussion around molecular cytogenetic findings.
Journal: European journal of medical genetics
Published: November 23, 2020
Population-based prevalence surveys during the Covid-19 pandemic: A systematic review.
Journal: Reviews in medical virology
Published: October 23, 2020
Candidate genes of oculo-auriculo-vertebral spectrum in 22q region: A systematic review.
Journal: American journal of medical genetics. Part A
Published: May 28, 2020
GATA 4 Deletions Associated with Congenital Heart Diseases in South Brazil.
Journal: Journal of pediatric genetics
Published: April 24, 2020
Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.
Journal: Journal of pediatric genetics
Published: February 20, 2020
Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review.
Journal: Journal of pediatric genetics
Published: January 13, 2020
Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case.
Journal: Journal of pediatric genetics
Published: November 20, 2019
Showing 1-12 of 12
Last Updated: 09/26/2026