Marta Unolt
6PUBLICATIONS
33CO-AUTHORS
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Publications (6)
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|Apr 22, 2024
Long-term incidence of arrhythmias in extracardiac conduit Fontan and comparison between systemic left and right ventricle.Corrado Di Mambro, Marie Laure Yammine, Pietro Paolo Tamborrino
|May 02, 2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literature.Gioia Mastromoro, Giulio Calcagni, Walter Vignaroli
|Sep 12, 2019
Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome.Martina Fanella, Marianna Frascarelli, Caterina Lambiase
|Sep 03, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.Marta Unolt, Molka Kammoun, Beata Nowakowska
|Nov 01, 2018
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.Ian M Campbell, Sarah E Sheppard, T Blaine Crowley
|Apr 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.Marta Unolt, Paolo Versacci, Silvia Anaclerio
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Frequent Collaborators
2 joint publications
T Blaine Crowley
1 joint publications
Maria Cristina Digilio
1 joint publications
Ian M Campbell
1 joint publications
Sarah E Sheppard
1 joint publications
Jelle F Homans
1 joint publications
Sarah E Hopkins
1 joint publications
Michele P Lambert
1 joint publications
Erica M Schindewolf
1 joint publications
Cynthia B Solot
1 joint publications
Kathleen E Sullivan
