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Magliozzi, Monia
45
results:
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Online (45)
Mediatypes
Articles (Online) (25)
OpenAccess-fulltext (20)
Sorted by: Relevance
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1
Partial atrioventricular canal defect and aortic coarctatio..:
Putotto, Carolina
;
Masci, Marco
;
Magliozzi, Monia
...
Birth Defects Research. 116 (2024) 7 - p. , 2024
Link:
https://doi.org/10.1002/..
?
2
A novel mutation in GAS8 gene associated with chronic rhino..:
Artesani, Maria Cristina
;
Santarsiero, Sara
;
Sitzia, Emanuela
...
Frontiers in Pediatrics. 12 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
3
Massive pericardial effusion in an infant with Aymé–Gripp s..:
Esposito, Arianna
;
Niceta, Marcello
;
Novelli, Antonio
...
American Journal of Medical Genetics Part A. 194 (2024) 9 - p. , 2024
Link:
https://doi.org/10.1002/..
?
4
FOXI3 pathogenic variants cause one form of craniofacial mi..:
Mao, Ke
;
Borel, Christelle
;
Ansar, Muhammad
...
Nature Communications. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
5
Biallelic truncating variants in children with titinopathy ..:
Baban, Anwar
;
Cicenia, Marianna
;
Magliozzi, Monia
...
Frontiers in Cardiovascular Medicine. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
6
Neonatal diagnosis of ACTA2‐related disease: A case report ..:
Lupo, Viviana
;
Di Gregorio, Maria Grazia
;
Mastrogiorgio, Gerarda
...
American Journal of Medical Genetics Part A. 191 (2023) 4 - p. 1111-1118 , 2023
Link:
https://doi.org/10.1002/..
?
7
PrenatalCFAP53-related laterality defect: case report and r..:
Mastromoro, Gioia
;
Guadagnolo, Daniele
;
Novelli, Antonio
...
The Journal of Maternal-Fetal & Neonatal Medicine. 36 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1080/..
?
8
A patient with mosaic USP9X gene variant:
Barili, Valeria
;
Dall'Asta, Andrea
;
Uliana, Vera
...
European Journal of Medical Genetics. 65 (2022) 12 - p. 104638 , 2022
Link:
https://doi.org/10.1016/..
?
9
Arrhythmogenic cardiomyopathy in children according to "Pad..:
Cicenia, Marianna
;
Cantarutti, Nicoletta
;
Adorisio, Rachele
...
International Journal of Cardiology. 350 (2022) - p. 83-89 , 2022
Link:
https://doi.org/10.1016/..
?
10
879 STUDY OF ATRIOVENTRICULAR CONDUCTION DEFECTS AND ARRHYT..:
Campisi, Mariapaola
;
Di Bella, Gianluca
;
De Gregorio, Cesare
...
European Heart Journal Supplements. 24 (2022) Supplement_K - p. , 2022
Link:
https://doi.org/10.1093/..
?
11
Cardiovascular Involvement in Pediatric FLNC Variants: A Ca..:
Baban, Anwar
;
Alesi, Viola
;
Magliozzi, Monia
...
Journal of Cardiovascular Development and Disease. 9 (2022) 10 - p. 332 , 2022
Link:
https://doi.org/10.3390/..
?
12
Clinical and molecular characterizations of 11 new patients..:
Tedesco, Maria Giovanna
;
Lonardo, Fortunato
;
Ceccarini, Caterina
...
American Journal of Medical Genetics Part A. 185 (2021) 4 - p. 1204-1210 , 2021
Link:
https://doi.org/10.1002/..
?
13
245 Arrhythmogenic cardiomyopathy in children according to ..:
Cicenia, Marianna
;
Cantarutti, Nicoletta
;
Adorisio, Rachele
...
European Heart Journal Supplements. 23 (2021) Supplement_G - p. , 2021
Link:
https://doi.org/10.1093/..
?
14
8p23.1 deletion: Look out for left ventricular hypertrabecu..:
Cicenia, Marianna
;
Alesi, Viola
;
Orlando, Valeria
...
American Journal of Medical Genetics Part A. 188 (2021) 3 - p. 883-895 , 2021
Link:
https://doi.org/10.1002/..
?
15
Cardiovascular Involvement in Pediatric Laminopathies. Repo..:
Baban, Anwar
;
Cicenia, Marianna
;
Magliozzi, Monia
...
Frontiers in Pediatrics. 8 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
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