Michele Callea
Florence, Italy
Last Updated: 09/26/2026
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Found 67 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
Main genetic entities associated with tooth agenesis.
Journal: Clinical oral investigations
Published: March 12, 2024
Dupilumab treatment of trichothiodystrophy in a child.
Journal: Pediatric dermatology
Published: October 28, 2023
Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.
Journal: Ophthalmic genetics
Published: September 27, 2023
Dermatological findings in Rubinstein-Taybi Syndrome.
Journal: Italian journal of dermatology and venereology
Published: June 07, 2023
Novel EDA mutations cause X-linked hypohidrotic ectodermal dysplasia: the first study from Venezuela.
Journal: Clinical and experimental dermatology
Published: March 25, 2023
Next generation sequencing panel target genes: possible diagnostic tool for ectodermal dysplasia related diseases.
Journal: Italian journal of dermatology and venereology
Published: March 20, 2023
Challenges in Communicating a Genetic Diagnosis.
Journal: Children (Basel, Switzerland)
Published: March 14, 2023
Extensive dental caries and periodontal disease in a child with GATA2 deficiency.
Journal: Journal of clinical and experimental dentistry
Published: January 24, 2023
Last Updated: 09/26/2026