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M Chiara

Showing results (61-70 of 151) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 3, 2016
Current Perspectives in Autism Spectrum Disorder: From Genes to TherapyMaria Chahrour, Brian J O'Roak, Emanuela Santini, et al.
Dermatologic Therapy|September 6, 2022
Complete response of locally advanced cutaneous squamous cell carcinoma of the eyelid to topical imiquimod 3.75Francesco Toso, M Chiara Tronconi, Andrea Cortese, et al.
Journal of Affective Disorders|January 27, 2006
Bulimia nervosa in atypical depression: the mediating role of cyclothymic temperamentGiulio Perugi, Cristina Toni, M Chiara Sanna Passino, et al.
Frontiers in Chemistry|April 25, 2022
Capillary Electrophoresis Mass Spectrometry for Scalable Single-Cell ProteomicsBowen Shen, Leena R Pade, Sam B Choi, et al.
Mechanisms of Ageing and Development|August 10, 2020
Atrial fibrillation and cognitive disorders: An overview on possible correlationDanilo Puccio, M Chiara Vizzini, Valentina Baiamonte, et al.
Jornal De Pediatria|December 20, 2003
[Peptic disease: comparative study between children and adolescents]M S Toporovski, C B Neufeld, A M Chiara, et al.
Biochimica Et Biophysica Acta|December 15, 2015
Langmuir monolayers and Differential Scanning Calorimetry for the study of the interactions between camptothecin drugs and biomembrane modelsAna Casadó, M Chiara Giuffrida, M Lluïsa Sagristá, et al.
Analytical Chemistry|May 13, 2025
A Multipoint Validation of Quantification in Capillary Electrophoresis Mass Spectrometry Proteomics: Isobaric Multiplexing with Tandem Mass TagsLaura G Rodriguez, Camille Lombard-Banek, Vi M Quach, et al.
Neurogenetics|January 31, 2024
Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 familiesSylvia Safwat, Kyle P Flannery, Ahmed A El Beheiry, et al.
Human Molecular Genetics|April 23, 2024
A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1AAniket Bhattacharya, Paola Parlanti, Luca Cavallo, et al.
Pageof 16

Showing results (61-70 of 151) with videos related to

Sort By:
Pageof 16
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 3, 2016
Current Perspectives in Autism Spectrum Disorder: From Genes to TherapyMaria Chahrour, Brian J O'Roak, Emanuela Santini, et al.
Dermatologic Therapy|September 6, 2022
Complete response of locally advanced cutaneous squamous cell carcinoma of the eyelid to topical imiquimod 3.75Francesco Toso, M Chiara Tronconi, Andrea Cortese, et al.
Journal of Affective Disorders|January 27, 2006
Bulimia nervosa in atypical depression: the mediating role of cyclothymic temperamentGiulio Perugi, Cristina Toni, M Chiara Sanna Passino, et al.
Frontiers in Chemistry|April 25, 2022
Capillary Electrophoresis Mass Spectrometry for Scalable Single-Cell ProteomicsBowen Shen, Leena R Pade, Sam B Choi, et al.
Mechanisms of Ageing and Development|August 10, 2020
Atrial fibrillation and cognitive disorders: An overview on possible correlationDanilo Puccio, M Chiara Vizzini, Valentina Baiamonte, et al.
Jornal De Pediatria|December 20, 2003
[Peptic disease: comparative study between children and adolescents]M S Toporovski, C B Neufeld, A M Chiara, et al.
Biochimica Et Biophysica Acta|December 15, 2015
Langmuir monolayers and Differential Scanning Calorimetry for the study of the interactions between camptothecin drugs and biomembrane modelsAna Casadó, M Chiara Giuffrida, M Lluïsa Sagristá, et al.
Analytical Chemistry|May 13, 2025
A Multipoint Validation of Quantification in Capillary Electrophoresis Mass Spectrometry Proteomics: Isobaric Multiplexing with Tandem Mass TagsLaura G Rodriguez, Camille Lombard-Banek, Vi M Quach, et al.
Neurogenetics|January 31, 2024
Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 familiesSylvia Safwat, Kyle P Flannery, Ahmed A El Beheiry, et al.
Human Molecular Genetics|April 23, 2024
A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1AAniket Bhattacharya, Paola Parlanti, Luca Cavallo, et al.
Pageof 16