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Carolina Putotto

Showing results (41-50 of 57) with videos related to

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American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Journal of Neuropsychology|May 9, 2023
Social cognition and real-life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controlsMarianna Frascarelli, Tommaso Accinni, Antonino Buzzanca, et al.
European Journal of Medical Genetics|November 21, 2022
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart diseaseCarolina Putotto, Marta Unolt, Caterina Lambiase, et al.
International Journal of Molecular Sciences|March 25, 2017
Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in TanzaniaSerena Caggiano, Nicola Ullmann, Elisa De Vitis, et al.
Heart Failure Clinics|November 15, 2021
Clinical Manifestations of 22q11.2 Deletion SyndromeAnnapaola Cirillo, Michele Lioncino, Annachiara Maratea, et al.
Diagnostics (Basel, Switzerland)|March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos SyndromeGiulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
Schizophrenia Bulletin Open|August 15, 2024
Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With SchizophreniaTommaso Accinni, Antonino Buzzanca, Marianna Frascarelli, et al.
European Heart Journal. Digital Health|July 14, 2026
Rational and design of the digital diagnosis of cardiac sounds in paediatric patients (DI_SOUND) studyGabriele Egidy Assenza, Alessandro Colombo, Vittoria Mastromarino, et al.
Genes|January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 MicrodeletionsNatalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Epilepsia|December 24, 2024
Phenotypic traits and family history in patients with 22q11.2 deletion syndrome and generalized epilepsy: A multicenter case-control studyEmanuele Cerulli Irelli, Martina Fanella, Boris Chaumette, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Journal of Neuropsychology|May 9, 2023
Social cognition and real-life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controlsMarianna Frascarelli, Tommaso Accinni, Antonino Buzzanca, et al.
European Journal of Medical Genetics|November 21, 2022
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart diseaseCarolina Putotto, Marta Unolt, Caterina Lambiase, et al.
International Journal of Molecular Sciences|March 25, 2017
Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in TanzaniaSerena Caggiano, Nicola Ullmann, Elisa De Vitis, et al.
Heart Failure Clinics|November 15, 2021
Clinical Manifestations of 22q11.2 Deletion SyndromeAnnapaola Cirillo, Michele Lioncino, Annachiara Maratea, et al.
Diagnostics (Basel, Switzerland)|March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos SyndromeGiulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
Schizophrenia Bulletin Open|August 15, 2024
Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With SchizophreniaTommaso Accinni, Antonino Buzzanca, Marianna Frascarelli, et al.
European Heart Journal. Digital Health|July 14, 2026
Rational and design of the digital diagnosis of cardiac sounds in paediatric patients (DI_SOUND) studyGabriele Egidy Assenza, Alessandro Colombo, Vittoria Mastromarino, et al.
Genes|January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 MicrodeletionsNatalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Epilepsia|December 24, 2024
Phenotypic traits and family history in patients with 22q11.2 deletion syndrome and generalized epilepsy: A multicenter case-control studyEmanuele Cerulli Irelli, Martina Fanella, Boris Chaumette, et al.
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