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Djouadi

Showing results (111-120 of 145) with videos related to

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American Journal of Human Genetics|April 17, 2007
Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromesN Dagoneau, S Bellais, P Blanchet, et al.
Journal of Personalized Medicine|July 2, 2021
Mitochondrial Fatty Acid β-Oxidation and Resveratrol Effect in Fibroblasts from Patients with Autism Spectrum DisorderRita Barone, Jean Bastin, Fatima Djouadi, et al.
Clinical Pharmacology and Therapeutics|May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiencyJ P Bonnefont, J Bastin, P Laforêt, et al.
ESC Heart Failure|June 24, 2022
Impact of cardiac resynchronization therapy optimization inside a heart failure programme: a real-world experienceThibaut Moulin, David Hamon, Kamila Djouadi, et al.
Human Molecular Genetics|April 27, 2011
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis modelsMairead Kelly-Aubert, Stéphanie Trudel, Janine Fritsch, et al.
World Journal of Microbiology & Biotechnology|October 14, 2025
Bacillus paralicheniformis strain H12 from saline soil for the management of gray mold in cherry tomatoesAmina Ghozlani, Fatma Driss, Duong Huy Nguyen, et al.
Oncogene|August 12, 2022
A proof of concept for targeting the PrP<sup>C</sup> - Amyloid β peptide interaction in basal prostate cancer and mesenchymal colon cancerSophie Mouillet-Richard, Séverine Martin-Lannerée, Delphine Le Corre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 6, 2022
Outbreak of hemolytic uremic syndrome with unusually severe clinical presentation caused by Shiga toxin-producing Escherichia coli O26:H11 in FranceK Minary, C Tanne, T Kwon, et al.
American Journal of Human Genetics|November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapyS Gobin-Limballe, F Djouadi, F Aubey, et al.
Clinical Genetics|September 13, 2008
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalitiesM Silvain, D Bligny, T Aparicio, et al.
Pageof 15

Showing results (111-120 of 145) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|April 17, 2007
Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromesN Dagoneau, S Bellais, P Blanchet, et al.
Journal of Personalized Medicine|July 2, 2021
Mitochondrial Fatty Acid β-Oxidation and Resveratrol Effect in Fibroblasts from Patients with Autism Spectrum DisorderRita Barone, Jean Bastin, Fatima Djouadi, et al.
Clinical Pharmacology and Therapeutics|May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiencyJ P Bonnefont, J Bastin, P Laforêt, et al.
ESC Heart Failure|June 24, 2022
Impact of cardiac resynchronization therapy optimization inside a heart failure programme: a real-world experienceThibaut Moulin, David Hamon, Kamila Djouadi, et al.
Human Molecular Genetics|April 27, 2011
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis modelsMairead Kelly-Aubert, Stéphanie Trudel, Janine Fritsch, et al.
World Journal of Microbiology & Biotechnology|October 14, 2025
Bacillus paralicheniformis strain H12 from saline soil for the management of gray mold in cherry tomatoesAmina Ghozlani, Fatma Driss, Duong Huy Nguyen, et al.
Oncogene|August 12, 2022
A proof of concept for targeting the PrP<sup>C</sup> - Amyloid β peptide interaction in basal prostate cancer and mesenchymal colon cancerSophie Mouillet-Richard, Séverine Martin-Lannerée, Delphine Le Corre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 6, 2022
Outbreak of hemolytic uremic syndrome with unusually severe clinical presentation caused by Shiga toxin-producing Escherichia coli O26:H11 in FranceK Minary, C Tanne, T Kwon, et al.
American Journal of Human Genetics|November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapyS Gobin-Limballe, F Djouadi, F Aubey, et al.
Clinical Genetics|September 13, 2008
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalitiesM Silvain, D Bligny, T Aparicio, et al.
Pageof 15