Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Chelly

Showing results (51-60 of 157) with videos related to

Pageof 16
Sort By:
Journal of Cardiovascular Pharmacology|January 1, 1980
Pharmacological properties of AR-C239, 2-[2-[4(o-methoxyphenyl)-piperazine-1-Yl]-ethyl]4,4-dimethyl-1,3(2H-4H) isoquinolinedione, a new alpha-adrenoceptor blocking drugP Mouillé, A M Huchet, J Chelly, et al.
Anesthesie, Analgesie, Reanimation|January 1, 1979
[Nitroglycerin and amyl nitrite action on common bile duct during operation for vesicular lithiasis (author's transl)]J Chelly, M L Tannières, D Tournay, et al.
Parkinsonism & Related Disorders|May 5, 2019
Novel anoctamin-3 missense mutation responsible for early-onset myoclonic dystoniaA Delamarre, J Chelly, D Guehl, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Striking conservation of the brain-specific region of the dystrophin geneJ P Hugnot, H Gilgenkrantz, M Jeanpierre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Mental retardation and disorders of cortical development]V Des Portes, J M Pinard, F Francis, et al.
Genomics|September 1, 1994
DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3)U Müller, G Haberhausen, T Wagner, et al.
Nature|March 1, 1990
Dystrophin gene transcribed from different promoters in neuronal and glial cellsJ Chelly, G Hamard, A Koulakoff, et al.
Neurology|November 9, 2000
Two affected boys in a Rett syndrome family: clinical and molecular findingsL Villard, A Kpebe, C Cardoso, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Parental origin of de novo MECP2 mutations in Rett syndromeM Girard, P Couvert, A Carrié, et al.
Anesthesie, Analgesie, Reanimation|January 1, 1979
[Prinzmetal's angina during myocardial revascularisation. Cardiovascular complications in 71 patients (author's transl)]B Fontaine, E Bertrandias, J Chelly, et al.
Pageof 16

Showing results (51-60 of 157) with videos related to

Sort By:
Pageof 16
Journal of Cardiovascular Pharmacology|January 1, 1980
Pharmacological properties of AR-C239, 2-[2-[4(o-methoxyphenyl)-piperazine-1-Yl]-ethyl]4,4-dimethyl-1,3(2H-4H) isoquinolinedione, a new alpha-adrenoceptor blocking drugP Mouillé, A M Huchet, J Chelly, et al.
Anesthesie, Analgesie, Reanimation|January 1, 1979
[Nitroglycerin and amyl nitrite action on common bile duct during operation for vesicular lithiasis (author's transl)]J Chelly, M L Tannières, D Tournay, et al.
Parkinsonism & Related Disorders|May 5, 2019
Novel anoctamin-3 missense mutation responsible for early-onset myoclonic dystoniaA Delamarre, J Chelly, D Guehl, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Striking conservation of the brain-specific region of the dystrophin geneJ P Hugnot, H Gilgenkrantz, M Jeanpierre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Mental retardation and disorders of cortical development]V Des Portes, J M Pinard, F Francis, et al.
Genomics|September 1, 1994
DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3)U Müller, G Haberhausen, T Wagner, et al.
Nature|March 1, 1990
Dystrophin gene transcribed from different promoters in neuronal and glial cellsJ Chelly, G Hamard, A Koulakoff, et al.
Neurology|November 9, 2000
Two affected boys in a Rett syndrome family: clinical and molecular findingsL Villard, A Kpebe, C Cardoso, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Parental origin of de novo MECP2 mutations in Rett syndromeM Girard, P Couvert, A Carrié, et al.
Anesthesie, Analgesie, Reanimation|January 1, 1979
[Prinzmetal's angina during myocardial revascularisation. Cardiovascular complications in 71 patients (author's transl)]B Fontaine, E Bertrandias, J Chelly, et al.
Pageof 16