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D Chateau

Showing results (41-50 of 53) with videos related to

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Annals of Neurology|May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibersM Villanova, J P Louboutin, D Chateau, et al.
Neurology|March 1, 1996
Oculopharyngeal muscular dystrophy in two unrelated Japanese familiesE Uyama, O Nohira, D Chateau, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Adult onset reducing body myopathyD Figarella-Branger, G A Putzu, C Bouvier-Labit, et al.
Nanoscale|December 23, 2014
From gold nanobipyramids to nanojavelins for a precise tuning of the plasmon resonance to the infrared wavelengths: experimental and theoretical aspectsD Chateau, A Liotta, F Vadcard, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in JapanE Uyama, O Nohira, F M Tomé, et al.
Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|October 27, 2019
Fluoroquinolone use for uncomplicated urinary tract infections in women: a retrospective cohort studyN Daneman, D Chateau, M Dahl, et al.
American Journal of Human Genetics|October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)C Donger, E Krejci, A P Serradell, et al.
Early Child Development and Care|January 30, 2015
Long-term benefits of full-day kindergarten: a longitudinal population-based studyM D Brownell, N C Nickel, D Chateau, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Annals of Neurology|May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibersM Villanova, J P Louboutin, D Chateau, et al.
Neurology|March 1, 1996
Oculopharyngeal muscular dystrophy in two unrelated Japanese familiesE Uyama, O Nohira, D Chateau, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Adult onset reducing body myopathyD Figarella-Branger, G A Putzu, C Bouvier-Labit, et al.
Nanoscale|December 23, 2014
From gold nanobipyramids to nanojavelins for a precise tuning of the plasmon resonance to the infrared wavelengths: experimental and theoretical aspectsD Chateau, A Liotta, F Vadcard, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in JapanE Uyama, O Nohira, F M Tomé, et al.
Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|October 27, 2019
Fluoroquinolone use for uncomplicated urinary tract infections in women: a retrospective cohort studyN Daneman, D Chateau, M Dahl, et al.
American Journal of Human Genetics|October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)C Donger, E Krejci, A P Serradell, et al.
Early Child Development and Care|January 30, 2015
Long-term benefits of full-day kindergarten: a longitudinal population-based studyM D Brownell, N C Nickel, D Chateau, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Pageof 6