Antonio Tadich-Cardenas
Antofagasta, AN, Chile
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
COVID-19 infection and intense physical activity in hypokalemic periodic paralysis.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: August 19, 2025
Legius Syndrome: the importance of molecular differential diagnosis with neurofibromatosis type 1.
Journal: Italian journal of dermatology and venereology
Published: April 02, 2025
Clinical and molecular findings in Cornelia de Lange syndrome. Case series.
Journal: Andes pediatrica : revista Chilena de pediatria
Published: December 02, 2024
Erratum: Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Journal: Journal of pediatric genetics
Published: July 12, 2024
Dermatological findings in Rubinstein-Taybi Syndrome.
Journal: Italian journal of dermatology and venereology
Published: June 07, 2023
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Journal: Journal of pediatric genetics
Published: February 10, 2021
Genetic variability in the case of COVID-19 infection.
Journal: Archivos argentinos de pediatria
Published: September 14, 2020
Trisomy 21 and the coronavirus disease 2019 (COVID-19).
Journal: Archivos argentinos de pediatria
Published: July 18, 2020
Clinical, etiopathogenic, and therapeutic aspects of KID syndrome.
Journal: Dermatologic therapy
Published: March 23, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026