Marzia Pollazzon

10PUBLICATIONS
35CO-AUTHORS
Neurology and neuromuscular diseasesNeonatologyGenetics not elsewhere classifiedOther language, communication and culture not elsewhere classifiedMedical biotechnology diagnostics (incl. biosensors)
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Publications (10)

|May 13, 2026
Phenotypic Heterogeneity in Titinopathies with Peripheral Nerve Involvement in Pediatric Age: Two Case Reports.

|Nov 27, 2025
A Boy with a Novel Variant in TCF20: An Expanded Phenotype and a Brief Review of the Literature.

Diletta Ziveri, Carlo Alberto Cesaroni, Gianluca Contrò

|Nov 13, 2025
Renal Hypoplasia and Oligomeganephronia in a Fetus with Wolf-Hirschhorn Syndrome.

Maria Paola Bonasoni, Mariangela Pati, Khush Shah

|Aug 26, 2023
Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes.

Irene Ambrosetti, Laura Bernardini, Marzia Pollazzon

|Jul 25, 2022
Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.

Ferdinand Dhombres, Patricia Morgan, Bimal P Chaudhari

|Apr 23, 2022
MCPH1: A Novel Case Report and a Review of the Literature.

Stefano Giuseppe Caraffi, Marzia Pollazzon, Muhammad Farooq

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Frequent Collaborators

8 joint publications

Stefano Giuseppe Caraffi

3 joint publications

Francesca Clementina Radio

3 joint publications

Carlo Fusco

2 joint publications

Susanna Rizzi