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Roberta Onesimo

Showing results (71-80 of 111) with videos related to

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Journal of Clinical Medicine|June 12, 2026
Use of Intravenous Immunoglobulins in Pediatric Viral Meningoencephalitis: A Real-World Retrospective Observational StudyIlaria Lazzareschi, Mariachiara Mercuri, Ludovica Renzelli, et al.
Genes|March 28, 2024
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the LiteratureValentina Trevisan, Anna Meroni, Chiara Leoni, et al.
Stem Cell Research|September 11, 2024
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome regionAngela Maria Giada Giovenale, Elisa Maria Turco, Martina Mazzoni, et al.
Archives of Disease in Childhood|May 16, 2022
Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patientsBeatrice Berti, Lavinia Fanelli, Giulia Stanca, et al.
Clinical Genetics|January 17, 2022
Prevalence of bladder cancer in Costello syndrome: New insights to drive clinical decision-makingChiara Leoni, Filomena Valentina Paradiso, Nazario Foschi, et al.
Genes|September 28, 2021
Epilepsy and <i>BRAF</i> Mutations: Phenotypes, Natural History and Genotype-Phenotype CorrelationsDomenica I Battaglia, Maria Luigia Gambardella, Stefania Veltri, et al.
European Journal of Medical Genetics|July 6, 2020
Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variantsFanny Kortüm, Marcello Niceta, Monia Magliozzi, et al.
Genes|January 21, 2023
What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative ReviewElisabetta Sforza, Gaia Margiotta, Valentina Giorgio, et al.
Genes|October 28, 2023
From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 SyndromeRoberta Onesimo, Elisabetta Sforza, Valentina Trevisan, et al.
European Journal of Medical Genetics|September 27, 2023
How pain affect real life of children and adults with achondroplasia: A systematic reviewRoberta Onesimo, Elisabetta Sforza, Maria Francesca Bedeschi, et al.
Pageof 12

Showing results (71-80 of 111) with videos related to

Sort By:
Pageof 12
Journal of Clinical Medicine|June 12, 2026
Use of Intravenous Immunoglobulins in Pediatric Viral Meningoencephalitis: A Real-World Retrospective Observational StudyIlaria Lazzareschi, Mariachiara Mercuri, Ludovica Renzelli, et al.
Genes|March 28, 2024
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the LiteratureValentina Trevisan, Anna Meroni, Chiara Leoni, et al.
Stem Cell Research|September 11, 2024
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome regionAngela Maria Giada Giovenale, Elisa Maria Turco, Martina Mazzoni, et al.
Archives of Disease in Childhood|May 16, 2022
Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patientsBeatrice Berti, Lavinia Fanelli, Giulia Stanca, et al.
Clinical Genetics|January 17, 2022
Prevalence of bladder cancer in Costello syndrome: New insights to drive clinical decision-makingChiara Leoni, Filomena Valentina Paradiso, Nazario Foschi, et al.
Genes|September 28, 2021
Epilepsy and <i>BRAF</i> Mutations: Phenotypes, Natural History and Genotype-Phenotype CorrelationsDomenica I Battaglia, Maria Luigia Gambardella, Stefania Veltri, et al.
European Journal of Medical Genetics|July 6, 2020
Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variantsFanny Kortüm, Marcello Niceta, Monia Magliozzi, et al.
Genes|January 21, 2023
What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative ReviewElisabetta Sforza, Gaia Margiotta, Valentina Giorgio, et al.
Genes|October 28, 2023
From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 SyndromeRoberta Onesimo, Elisabetta Sforza, Valentina Trevisan, et al.
European Journal of Medical Genetics|September 27, 2023
How pain affect real life of children and adults with achondroplasia: A systematic reviewRoberta Onesimo, Elisabetta Sforza, Maria Francesca Bedeschi, et al.
Pageof 12