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Daniela Concolino

Showing results (61-70 of 80) with videos related to

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Analytical Biochemistry|July 17, 2018
Composition and structure of glycosaminoglycans in DBS from 2-3-day-old newborns for the diagnosis of mucopolysaccharidosisFrancesca Maccari, Fabio Galeotti, Veronica Mantovani, et al.
Clinical Immunology (Orlando, Fla.)|January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief|March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Oncotarget|November 9, 2016
Genetic variants associated with gastrointestinal symptoms in Fabry diseaseMaria Teresa Di Martino, Francesca Scionti, Simona Sestito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 5, 2017
Early diagnosis of mucopolysaccharidoses in developing countries: A low cost and easy execution approachOrazio Gabrielli, Lucia Zampini, Chiara Monachesi, et al.
Genes|June 26, 2026
Expanding the Mutational Spectrum of <i>ACADVL</i>: Integrative Characterization of the p.Ser72Phe Variant in Very Long-Chain Acyl-CoA Dehydrogenase DeficiencyFrancesca Dinatolo, Lucia D'Antona, Radha Procopio, et al.
European Journal of Neurology|September 14, 2021
Epilepsy, electroclinical features, and long-term outcomes in Pitt-Hopkins syndrome due to pathogenic variants in the TCF4 geneSara Matricardi, Paolo Bonanni, Giulia Iapadre, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 29, 2023
Cerebral and systemic near infrared spectroscopy patterns in preterm infants treated by caffeineChiara Strozzi, Caterina Di Battista, Alessandro Graziosi, et al.
Epilepsy & Behavior : E&B|November 5, 2019
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up studyGiulia Iapadre, Luca Zagaroli, Nicola Cimini, et al.
Orphanet Journal of Rare Diseases|February 10, 2018
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapyRossella Parini, Paola De Lorenzo, Andrea Dardis, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Analytical Biochemistry|July 17, 2018
Composition and structure of glycosaminoglycans in DBS from 2-3-day-old newborns for the diagnosis of mucopolysaccharidosisFrancesca Maccari, Fabio Galeotti, Veronica Mantovani, et al.
Clinical Immunology (Orlando, Fla.)|January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief|March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis diseaseLaura Dotta, Omar Scomodon, Rita Padoan, et al.
Oncotarget|November 9, 2016
Genetic variants associated with gastrointestinal symptoms in Fabry diseaseMaria Teresa Di Martino, Francesca Scionti, Simona Sestito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 5, 2017
Early diagnosis of mucopolysaccharidoses in developing countries: A low cost and easy execution approachOrazio Gabrielli, Lucia Zampini, Chiara Monachesi, et al.
Genes|June 26, 2026
Expanding the Mutational Spectrum of <i>ACADVL</i>: Integrative Characterization of the p.Ser72Phe Variant in Very Long-Chain Acyl-CoA Dehydrogenase DeficiencyFrancesca Dinatolo, Lucia D'Antona, Radha Procopio, et al.
European Journal of Neurology|September 14, 2021
Epilepsy, electroclinical features, and long-term outcomes in Pitt-Hopkins syndrome due to pathogenic variants in the TCF4 geneSara Matricardi, Paolo Bonanni, Giulia Iapadre, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 29, 2023
Cerebral and systemic near infrared spectroscopy patterns in preterm infants treated by caffeineChiara Strozzi, Caterina Di Battista, Alessandro Graziosi, et al.
Epilepsy & Behavior : E&B|November 5, 2019
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up studyGiulia Iapadre, Luca Zagaroli, Nicola Cimini, et al.
Orphanet Journal of Rare Diseases|February 10, 2018
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapyRossella Parini, Paola De Lorenzo, Andrea Dardis, et al.
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