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검색어 [키워드: "Mandarino, Alessandra"]

1

PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports

학술저널

issue: FRONTIERS IN PSYCHIATRY; JAN 15 2024, 14 p1327802 13p.
Author: Montanaro, Federica Alice Maria
Mandarino, Alessandra
Alesi, Viola
Schwartz, Charles
Sepulveda, Daniela Judith Claps
Skinner, Cindy
Friez, Michael
Piccolo, Gabriele
Novelli, Antonio
Zanni, Ginevra
Dentici, Maria Lisa
Vicari, Stefano
Alfieri, Paolo
DB Label: Database : Science Citation Index Expanded

원문보기: 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science

2

D-aspartate oxidase gene duplication induces social recognition memory deficit in mice and intellectual disabilities in humans

학술저널

issue: Translational Psychiatry. 12(1)
Author: Lombardo, Barbara^{Aff1, Aff2}
Pagani, Marco
De Rosa, Arianna
Nunziato, Marcella^{Aff1, Aff2}
Migliarini, Sara
Garofalo, Martina^{Aff1, Aff5}
Terrile, Marta^{Aff6, Aff16}
D’Argenio, Valeria^{Aff1, Aff7}
Galbusera, Alberto
Nuzzo, Tommaso^{Aff1, Aff5}
Ranieri, Annaluisa^{Aff1, Aff2}
Vitale, Andrea^{Aff1, Aff2}
Leggiero, Eleonora
Di Maio, Anna
Barsotti, Noemi
Borello, Ugo
Napolitano, Francesco^{Aff1, Aff8}
Mandarino, Alessandra
Carotenuto, Marco
Heresco-Levy, Uriel^{Aff10, Aff11}
Pasqualetti, Massimo^{Aff3, Aff4}
Malatesta, Paolo^{Aff12, Aff13}
Gozzi, Alessandro
Errico, Francesco^{Aff1, Aff14}
Salvatore, Francesco^{Aff1, Aff15, IDs41398022020885_cor25}
Pastore, Lucio^{Aff1, Aff2, IDs41398022020885_cor26}
Usiello, Alessandro^{Aff1, Aff5, IDs41398022020885_cor27}
DB Label: Database : Springer Nature Journals

원문보기: OA (Springer) OA (Nature) 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science (SCIE)

3

PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.

학술저널

issue: Frontiers in Psychiatry; 2024, p1-13, 13p
Author: Montanaro, Federica Alice Maria
Mandarino, Alessandra
Alesi, Viola
Schwartz, Charles
Sepulveda, Daniela Judith Claps
Skinner, Cindy
Friez, Michael
Piccolo, Gabriele
Novelli, Antonio
Zanni, Ginevra
Dentici, Maria Lisa
Vicari, Stefano
Alfieri, Paolo
DB Label: Database : Complementary Index

원문보기: 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science (SCIE)

4

Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness

학술저널

issue: CLINICAL GENETICS; JUL 17 2023, 14p.
Author: Sinibaldi, Lorenzo
Garone, Giacomo
Mandarino, Alessandra
Iarossi, Giancarlo
Chioma, Laura
Dentici, Marialisa
Merla, Giuseppe
Agolini, Emanuele
Micalizzi, Alessia
Mancini, Cecilia
Niceta, Marcello
Macchiaiolo, Marina
Diodato, Daria
Onesimo, Roberta
Blandino, Rita
Delogu, Angelica Bibiana
De Rosa, Gabriella
Trevisan, Valentina
Iademarco, Mariella
Zampino, Giuseppe
Tartaglia, Marco
Novelli, Antonio
Bartuli, Andrea
Digilio, Maria Cristina
Calcagni, Giulio
DB Label: Database : Science Citation Index Expanded

원문보기: Full Text (Wiley-DB) 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science 원문복사신청 - RISS

5

Characterization of Sleep Disturbances in Children and Adolescents with Down Syndrome and Their Relation with Cognitive and Behavioral Features

학술저널

issue: INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH; MAY 2021, 18 9, p5001 14p.
Author: Fuca, Elisa
Costanzo, Floriana
Celestini, Laura
Mandarino, Alessandra
Vicari, Stefano
DB Label: Database : Science Citation Index Expanded

원문보기: 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science

6

Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.

issue: Frontiers in psychiatry [Front Psychiatry] 2024 Feb 13; Vol. 15, pp. 1375954. Date of Electronic Publication: 2024 Feb 13 (Print Publication: 2024).
Author: Montanaro FAM; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Mandarino A; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Alesi V; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Schwartz C; Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI, United States.
Sepulveda DJC; Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Skinner C; Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States.
Friez M; Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States.
Piccolo G; Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Novelli A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Zanni G; Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Dentici ML; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Vicari S; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Alfieri P; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
DB Label: Database : MEDLINE

원문보기: Open Access (PubMed Central) 등재 - SCOPUS 조회 - Impact Factor (JCR) 등재 - Web of Science (SCIE)

1

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