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Julien Baruteau

Showing results (1-10 of 68) with videos related to

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Journal of Inherited Metabolic Disease|June 13, 2025
First in Human Gene Editing for an Inherited Metabolic DiseaseShamima Rahman, Julien Baruteau
NPJ Regenerative Medicine|September 26, 2022
Modelling urea cycle disorders using iPSCsClaire Duff, Julien Baruteau
Frontiers in Pharmacology|October 17, 2022
Inherited and acquired vitamin B12 deficiencies: Which administration route to choose for supplementation?Ramyia Elangovan, Julien Baruteau
Journal of Inherited Metabolic Disease|February 5, 2019
Fetal gene therapy for neurodegenerative lysosomal storage diseasesJulien Baruteau, Simon N Waddington
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
Dorsolumbar kyphosis: diagnostic value of hook shaped vertebraJulien Baruteau, Hélène Ogier de Baulny
Cardiology in the Young|January 14, 2010
The differential diagnosis of primary electrical diseases from seizures in childhoodAlban-Elouen Baruteau, Julien Baruteau, Philippe Mabo
Journal of Inherited Metabolic Disease|January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseasesJulien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease|April 7, 2023
Gene therapy for urea cycle defects: An update from historical perspectives to future prospectsClaire Duff, Ian E Alexander, Julien Baruteau
Journal of Inherited Metabolic Disease|January 3, 2024
Liver-directed gene therapy for inherited metabolic diseasesJulien Baruteau, Nicola Brunetti-Pierri, Paul Gissen
Cell Communication and Signaling : CCS|April 24, 2021
The exosome journey: from biogenesis to uptake and intracellular signallingSonam Gurung, Dany Perocheau, Loukia Touramanidou, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|June 13, 2025
First in Human Gene Editing for an Inherited Metabolic DiseaseShamima Rahman, Julien Baruteau
NPJ Regenerative Medicine|September 26, 2022
Modelling urea cycle disorders using iPSCsClaire Duff, Julien Baruteau
Frontiers in Pharmacology|October 17, 2022
Inherited and acquired vitamin B12 deficiencies: Which administration route to choose for supplementation?Ramyia Elangovan, Julien Baruteau
Journal of Inherited Metabolic Disease|February 5, 2019
Fetal gene therapy for neurodegenerative lysosomal storage diseasesJulien Baruteau, Simon N Waddington
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
Dorsolumbar kyphosis: diagnostic value of hook shaped vertebraJulien Baruteau, Hélène Ogier de Baulny
Cardiology in the Young|January 14, 2010
The differential diagnosis of primary electrical diseases from seizures in childhoodAlban-Elouen Baruteau, Julien Baruteau, Philippe Mabo
Journal of Inherited Metabolic Disease|January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseasesJulien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease|April 7, 2023
Gene therapy for urea cycle defects: An update from historical perspectives to future prospectsClaire Duff, Ian E Alexander, Julien Baruteau
Journal of Inherited Metabolic Disease|January 3, 2024
Liver-directed gene therapy for inherited metabolic diseasesJulien Baruteau, Nicola Brunetti-Pierri, Paul Gissen
Cell Communication and Signaling : CCS|April 24, 2021
The exosome journey: from biogenesis to uptake and intracellular signallingSonam Gurung, Dany Perocheau, Loukia Touramanidou, et al.
Pageof 7