Matteo Cassina (M Cassina)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 11

Top Venues

Audiology research

Genes

Cancers

Journal of nephrology

Università degli Studi di Padova

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Università degli Studi di Padova

Italy

MD, Fixed-Term Assistant Professor in Medical Genetics :: Department of Women's and Children's Health

Publications

Ugo Sorrentino, Ilaria Gabbiato, Chiara Canciani, Davide Calosci, Chiara Rigon, Daniela Zuccarello, Matteo Cassina
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature. Genes 14 (3) (2023)
Ugo Sorrentino, Ilaria Gabbiato, Chiara Canciani, Davide Calosci, Chiara Rigon, Daniela Zuccarello, Matteo Cassina
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature. Genes 14 (3) (2023)
Ugo Sorrentino, Ilaria Gabbiato, Chiara Canciani, Davide Calosci, Chiara Rigon, Daniela Zuccarello, Matteo Cassina
Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature. Genes 14 (3) (2023)
Elena Cacciatori, Sebastiano Aleo, Giulietta Scuvera, Chiara Rigon, Paola Giovanna Marchisio, Matteo Cassina, Donatella Milani
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report. Italian journal of pediatrics 48 (1) (2022)
Alessandro Martini, Matteo Cassina
Correction: Martini, A.; Cassina, M. Victor A. McKusick, the "Father of Medical Genetics". Audiol. Res. 2021, 11 , 636-638. Audiology research 12 (1) (2022)
Alessandro Martini, Flavia Sorrentino, Ugo Sorrentino, Matteo Cassina
Genetics & Epigenetics of Hereditary Deafness: An Historical Overview. Audiology research 11 (4) (2021)
Ugo Sorrentino, Chiara Piccolo, Chiara Rigon, Valeria Brasson, Eva Trevisson, Francesca Boaretto, Alessandro Martini, Matteo Cassina
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature. Audiology research 11 (4) (2021)
Ugo Sorrentino, Silvia Bellonzi, Chiara Mozzato, Valeria Brasson, Irene Toldo, Raffaele Parrozzani, Maurizio Clementi, Matteo Cassina, Eva Trevisson
Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 Patients. Cancers 13 (24) (2021)
Franca Anglani, Leonardo Salviati, Matteo Cassina, Matteo Rigato, Laura Gobbi, Lorenzo Arcangelo Calò
Genotype-phenotype correlation in Gordon's syndrome: report of two cases carrying novel heterozygous mutations. Journal of nephrology (2021)
Alessandro Martini, Matteo Cassina
Victor A. McKusick, the "Father of Medical Genetics". Audiology research 11 (4) (2021)
G Bottesi, A Spoto, E Trevisson, D Zuccarello, G Vidotto, Matteo Cassina, M Clementi
Dysfunctional coping is related to impaired skin-related quality of life and psychological distress in patients with neurofibromatosis type 1 with major skin involvement. The British journal of dermatology 182 (6) (2019)

Matteo Cassina.css-eqlu8i{font-size:small;padding-left:4px;} (M Cassina)

Publication Activity (10 Years)

Top Topics

Top Venues

Matteo Cassina (M Cassina)