Maria Lisa Dentici

38PUBLICATIONS
133CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)NeurogeneticsNeonatologyGene and molecular therapy
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Publications (38)

|Jun 26, 2026
Multisystemic Assessment in Andersen-Tawil Syndrome: Report of Eighteen Individuals.

|Sep 27, 2025
Congenital Diaphragmatic Hernia and Joint Laxity: A Putative Link with Heritable Connective Tissue Disorders.

Alessandra Di Pede, Monia Magliozzi, Laura Valfré

|Jun 29, 2025
Further Exploring the TRRAP Genotype-Phenotype Correlations: Report of Three New Patients With A Focus on Skeletal Anomalies.

Chiara Minotti, Sara Terreri, Andrea Del Fattore

|Apr 25, 2025
Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B -Related Disorders: Case Series and Review of the Literature.

Vittorio Maglione, Antonio Pizzuti, Gioia Mastromoro

|Jan 31, 2025
MTSS2 -Related Disorder: Refining the Phenotype in Four New Cases and Literature Review.

Angela De Dominicis, Francesca Piceci Sparascio, Fabrizia Stregapede

|Dec 23, 2024
TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann

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Frequent Collaborators

9 joint publications

Maria Cristina Digilio

7 joint publications

Sara Loddo

6 joint publications

Marco Tartaglia

6 joint publications

Viola Alesi