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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 syndromes
N 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 Disorder
Rita 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 deficiency
J 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 experience
Thibaut Moulin, David Hamon, Kamila Djouadi, et al.
Human Molecular Genetics
|
April 27, 2011
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models
Mairead 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 tomatoes
Amina 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 cancer
Sophie 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 France
K 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 therapy
S 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 abnormalities
M Silvain, D Bligny, T Aparicio, et al.
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of 15
Search research articles
Search
Showing results (111-120 of 145) with videos related to
Sort By:
Page
of 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 syndromes
N 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 Disorder
Rita 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 deficiency
J 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 experience
Thibaut Moulin, David Hamon, Kamila Djouadi, et al.
Human Molecular Genetics
|
April 27, 2011
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models
Mairead 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 tomatoes
Amina 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 cancer
Sophie 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 France
K 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 therapy
S 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 abnormalities
M Silvain, D Bligny, T Aparicio, et al.
Page
of 15