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Irene Bruno

Showing results (31-40 of 61) with videos related to

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Journal of Pediatric Hematology/Oncology|December 14, 2005
Attitudes of children with leukemia toward repeated deep sedations with propofolEgidio Barbi, Laura Badina, Federico Marchetti, et al.
Frontiers in Pediatrics|August 29, 2025
Severe tenosynovitis with rapidly fluctuating power Doppler activity, a clue for the diagnosis of Blau syndrome: a case reportSerena Pastore, Carolina Carraro, Eleonora De Martino, et al.
Archives of Pediatrics & Adolescent Medicine|November 12, 2003
Deep sedation with propofol by nonanesthesiologists: a prospective pediatric experienceEgidio Barbi, Tania Gerarduzzi, Federico Marchetti, et al.
Journal of Inherited Metabolic Disease|February 28, 2023
Long-term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha-mannosidosis: A phase 2, open label, multicenter studyNathalie Guffon, Vassiliki Konstantopoulou, Julia B Hennermann, et al.
Neuromuscular Disorders : NMD|November 29, 2023
A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNA<sup>Pro</sup>Elena Ghirigato, Francesca Terenzi, Mirko Baglivo, et al.
Paediatric Drugs|December 18, 2022
Characterization of Cardiac Function by Echocardiographic Global Longitudinal Strain in a Cohort of Children with Neurofibromatosis Type 1 Treated with SelumetinibThomas Caiffa, Antimo Tessitore, Andrea Magnolato, et al.
Molecular Genetics & Genomic Medicine|January 11, 2019
Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysisRoberta Bottega, Stefania Cappellani, Antonella Fabretto, et al.
Paediatric Drugs|June 14, 2020
Selumetinib in the Treatment of Symptomatic Intractable Plexiform Neurofibromas in Neurofibromatosis Type 1: A Prospective Case Series with Emphasis on Side EffectsFrancesco Baldo, Antonio Giacomo Grasso, Luisa Cortellazzo Wiel, et al.
Healthcare (Basel, Switzerland)|July 14, 2023
Measuring Knowledge of Healthcare Providers on Pediatric Palliative Care with an Online Questionnaire Based on the National Core Curriculum in ItalyElisa Zanello, Roberta Vecchi, Giulia Zamagni, et al.
Gene|December 26, 2012
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: clinical and functional characterization of two novel ABCC8 mutationsFlavio Faletra, Kara Snider, Show-Ling Shyng, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Journal of Pediatric Hematology/Oncology|December 14, 2005
Attitudes of children with leukemia toward repeated deep sedations with propofolEgidio Barbi, Laura Badina, Federico Marchetti, et al.
Frontiers in Pediatrics|August 29, 2025
Severe tenosynovitis with rapidly fluctuating power Doppler activity, a clue for the diagnosis of Blau syndrome: a case reportSerena Pastore, Carolina Carraro, Eleonora De Martino, et al.
Archives of Pediatrics & Adolescent Medicine|November 12, 2003
Deep sedation with propofol by nonanesthesiologists: a prospective pediatric experienceEgidio Barbi, Tania Gerarduzzi, Federico Marchetti, et al.
Journal of Inherited Metabolic Disease|February 28, 2023
Long-term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha-mannosidosis: A phase 2, open label, multicenter studyNathalie Guffon, Vassiliki Konstantopoulou, Julia B Hennermann, et al.
Neuromuscular Disorders : NMD|November 29, 2023
A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNA<sup>Pro</sup>Elena Ghirigato, Francesca Terenzi, Mirko Baglivo, et al.
Paediatric Drugs|December 18, 2022
Characterization of Cardiac Function by Echocardiographic Global Longitudinal Strain in a Cohort of Children with Neurofibromatosis Type 1 Treated with SelumetinibThomas Caiffa, Antimo Tessitore, Andrea Magnolato, et al.
Molecular Genetics & Genomic Medicine|January 11, 2019
Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysisRoberta Bottega, Stefania Cappellani, Antonella Fabretto, et al.
Paediatric Drugs|June 14, 2020
Selumetinib in the Treatment of Symptomatic Intractable Plexiform Neurofibromas in Neurofibromatosis Type 1: A Prospective Case Series with Emphasis on Side EffectsFrancesco Baldo, Antonio Giacomo Grasso, Luisa Cortellazzo Wiel, et al.
Healthcare (Basel, Switzerland)|July 14, 2023
Measuring Knowledge of Healthcare Providers on Pediatric Palliative Care with an Online Questionnaire Based on the National Core Curriculum in ItalyElisa Zanello, Roberta Vecchi, Giulia Zamagni, et al.
Gene|December 26, 2012
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: clinical and functional characterization of two novel ABCC8 mutationsFlavio Faletra, Kara Snider, Show-Ling Shyng, et al.
Pageof 7