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Showing results (341-350 of 347) with videos related to

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Italian Journal of Pediatrics|June 13, 2026
Impact of regional heterogeneity of RSV infection prophylaxis on bronchiolitis in ItalyRaffaele Badolato, Viola Ceconi, Roberto Bellu', et al.
Human Mutation|December 30, 2014
Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutationsAnna Caciotti, Rodolfo Tonin, Miriam Rigoldi, et al.
Endocrine|February 6, 2025
Hypophosphatemic rickets in an Italian multicentric cohort of 24 subjects: a clinical and molecular characterisationR Chimenz, C Columbu, F Pugliese, et al.
Orphanet Journal of Rare Diseases|November 29, 2025
Late-onset Pompe's disease in pediatrics: results from an Italian national survey on 38 patients and proposal of a targeted diagnostic algorithmMarco Spada, Serena Gasperini, Massimiliano Filosto, et al.
Journal for Immunotherapy of Cancer|February 18, 2021
Therapeutic afucosylated monoclonal antibody and bispecific T-cell engagers for T-cell acute lymphoblastic leukemiaDaniele Caracciolo, Caterina Riillo, Andrea Ballerini, et al.
Journal of the American College of Cardiology|September 3, 2016
Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty ClinicsValentina Favalli, Eliana Disabella, Mariadelfina Molinaro, et al.
Human Mutation|May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classificationMichael T Parsons, Emma Tudini, Hongyan Li, et al.
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Showing results (341-350 of 347) with videos related to

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You have reached the last page of results.This site can display upto 347 results.
Italian Journal of Pediatrics|June 13, 2026
Impact of regional heterogeneity of RSV infection prophylaxis on bronchiolitis in ItalyRaffaele Badolato, Viola Ceconi, Roberto Bellu', et al.
Human Mutation|December 30, 2014
Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutationsAnna Caciotti, Rodolfo Tonin, Miriam Rigoldi, et al.
Endocrine|February 6, 2025
Hypophosphatemic rickets in an Italian multicentric cohort of 24 subjects: a clinical and molecular characterisationR Chimenz, C Columbu, F Pugliese, et al.
Orphanet Journal of Rare Diseases|November 29, 2025
Late-onset Pompe's disease in pediatrics: results from an Italian national survey on 38 patients and proposal of a targeted diagnostic algorithmMarco Spada, Serena Gasperini, Massimiliano Filosto, et al.
Journal for Immunotherapy of Cancer|February 18, 2021
Therapeutic afucosylated monoclonal antibody and bispecific T-cell engagers for T-cell acute lymphoblastic leukemiaDaniele Caracciolo, Caterina Riillo, Andrea Ballerini, et al.
Journal of the American College of Cardiology|September 3, 2016
Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty ClinicsValentina Favalli, Eliana Disabella, Mariadelfina Molinaro, et al.
Human Mutation|May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classificationMichael T Parsons, Emma Tudini, Hongyan Li, et al.
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