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Chabrier

Showing results (431-440 of 502) with videos related to

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Annals of Physical and Rehabilitation Medicine|August 18, 2019
From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand?Stéphane Chabrier, Margaux Pouyfaucon, Alain Chatelin, et al.
Plos One|July 8, 2017
Correction: Immuno-related polymorphisms and cervical cancer risk: The IARC multicentric case-control studyJames McKay, Vanessa Tenet, Silvia Franceschi, et al.
Bioorganic & Medicinal Chemistry Letters|January 20, 2007
Butyl 2-(4-[1.1'-biphenyl]-4-yl-1H-imidazol-2-yl)ethylcarbamate, a potent sodium channel blocker for the treatment of neuropathic painAnne-Marie Liberatore, Jocelyne Schulz, Christine Favre-Guilmard, et al.
British Journal of Pharmacology|August 1, 2015
Combining citrulline with atorvastatin preserves glucose homeostasis in a murine model of diet-induced obesityFrédéric Capel, Gwladys Chabrier, Elodie Pitois, et al.
Endocrine-Related Cancer|November 30, 2016
Successful response to pegylated interferon alpha in a patient with recurrent paragangliomaThibault Bahougne, Alessio Imperiale, Gerlinde Averous, et al.
Royal Society Open Science|November 21, 2015
Yes, it turns: experimental evidence of pearl rotation during its formationYannick Gueguen, Yann Czorlich, Max Mastail, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 5, 2017
Head-to-head comparison between <sup>18</sup>F-FDOPA PET/CT and MR/CT angiography in clinically recurrent head and neck paragangliomasCéline Heimburger, Francis Veillon, David Taïeb, et al.
The Journal of Pediatrics|March 13, 2016
Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic StrokeStéphane Chabrier, Emeline Peyric, Laure Drutel, et al.
Molecular Genetics and Metabolism|January 31, 2006
D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?E A Struys, N M Verhoeven, G S Salomons, et al.
Genes, Chromosomes & Cancer|July 10, 2013
Association between TP53 R249S mutation and polymorphisms in TP53 intron 1 in hepatocellular carcinomaSandra Ortiz-Cuaran, David Cox, Stéphanie Villar, et al.
Pageof 51

Showing results (431-440 of 502) with videos related to

Sort By:
Pageof 51
Annals of Physical and Rehabilitation Medicine|August 18, 2019
From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand?Stéphane Chabrier, Margaux Pouyfaucon, Alain Chatelin, et al.
Plos One|July 8, 2017
Correction: Immuno-related polymorphisms and cervical cancer risk: The IARC multicentric case-control studyJames McKay, Vanessa Tenet, Silvia Franceschi, et al.
Bioorganic & Medicinal Chemistry Letters|January 20, 2007
Butyl 2-(4-[1.1'-biphenyl]-4-yl-1H-imidazol-2-yl)ethylcarbamate, a potent sodium channel blocker for the treatment of neuropathic painAnne-Marie Liberatore, Jocelyne Schulz, Christine Favre-Guilmard, et al.
British Journal of Pharmacology|August 1, 2015
Combining citrulline with atorvastatin preserves glucose homeostasis in a murine model of diet-induced obesityFrédéric Capel, Gwladys Chabrier, Elodie Pitois, et al.
Endocrine-Related Cancer|November 30, 2016
Successful response to pegylated interferon alpha in a patient with recurrent paragangliomaThibault Bahougne, Alessio Imperiale, Gerlinde Averous, et al.
Royal Society Open Science|November 21, 2015
Yes, it turns: experimental evidence of pearl rotation during its formationYannick Gueguen, Yann Czorlich, Max Mastail, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 5, 2017
Head-to-head comparison between <sup>18</sup>F-FDOPA PET/CT and MR/CT angiography in clinically recurrent head and neck paragangliomasCéline Heimburger, Francis Veillon, David Taïeb, et al.
The Journal of Pediatrics|March 13, 2016
Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic StrokeStéphane Chabrier, Emeline Peyric, Laure Drutel, et al.
Molecular Genetics and Metabolism|January 31, 2006
D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?E A Struys, N M Verhoeven, G S Salomons, et al.
Genes, Chromosomes & Cancer|July 10, 2013
Association between TP53 R249S mutation and polymorphisms in TP53 intron 1 in hepatocellular carcinomaSandra Ortiz-Cuaran, David Cox, Stéphanie Villar, et al.
Pageof 51