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B Echenne

Showing results (81-90 of 121) with videos related to

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Archives Francaises De Pediatrie|June 1, 1983
[Use of diazepam in the preventive home treatment of recurrent febrile convulsions]B Echenne, R Cheminal, P Martin, et al.
Archives Francaises De Pediatrie|August 1, 1984
[Dystonia musculorum deformans. Elements of a favorable development]J P Visier, M Maury, C Maurin, et al.
Human Genetics|December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophiesM Claustres, S Tuffery, M P Chevron, et al.
Brain & Development|April 13, 2000
Perturbation in dystrophin-associated glycoprotein complex in a boy with Becker muscular dystrophyF Rivier, B Echenne, Y Chaix, et al.
Brain & Development|January 12, 2010
Unexpected neurological sequelae following propofol anesthesia in infants: Three case reportsP Meyer, C Langlois, S Soëte, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Neuropediatrics|February 1, 1989
Encephalopathy with calcifications of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new casesC Billard, O Dulac, J Bouloche, et al.
Brain & Development|November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)A Roubertie, M Semprino, A M Chaze, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Dystrophin superfamily complexes are different in muscle and the nervous systemE Fabbrizio, F Rivier, A Bonet-Kerrache, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Ectopic intraspinal extradural anaplastic ependymoma in an infant]A Roubertie, P Coubes, V Humbertclaude, et al.
Pageof 13

Showing results (81-90 of 121) with videos related to

Sort By:
Pageof 13
Archives Francaises De Pediatrie|June 1, 1983
[Use of diazepam in the preventive home treatment of recurrent febrile convulsions]B Echenne, R Cheminal, P Martin, et al.
Archives Francaises De Pediatrie|August 1, 1984
[Dystonia musculorum deformans. Elements of a favorable development]J P Visier, M Maury, C Maurin, et al.
Human Genetics|December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophiesM Claustres, S Tuffery, M P Chevron, et al.
Brain & Development|April 13, 2000
Perturbation in dystrophin-associated glycoprotein complex in a boy with Becker muscular dystrophyF Rivier, B Echenne, Y Chaix, et al.
Brain & Development|January 12, 2010
Unexpected neurological sequelae following propofol anesthesia in infants: Three case reportsP Meyer, C Langlois, S Soëte, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Neuropediatrics|February 1, 1989
Encephalopathy with calcifications of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new casesC Billard, O Dulac, J Bouloche, et al.
Brain & Development|November 27, 2001
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)A Roubertie, M Semprino, A M Chaze, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Dystrophin superfamily complexes are different in muscle and the nervous systemE Fabbrizio, F Rivier, A Bonet-Kerrache, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Ectopic intraspinal extradural anaplastic ependymoma in an infant]A Roubertie, P Coubes, V Humbertclaude, et al.
Pageof 13