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B Echenne

Showing results (91-100 of 121) with videos related to

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Revue Neurologique|May 2, 2002
[The varied etiologies of childhood-onset dystonia]A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]V Humbertclaude, S Tourtet, M Semprino, et al.
Neurology|May 22, 1998
Congenital muscular dystrophy and cerebellar atrophyB Echenne, F Rivier, M Tardieu, et al.
Neuro-Chirurgie|August 17, 1999
[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case]P Coubes, B Echenne, A Roubertie, et al.
Annales De Pediatrie|May 1, 1984
[Chloramphenicol treatment of Haemophilus influenzae meningitis in the child]B Echenne, R Cheminal, F Rapin, et al.
Human Genetics|April 4, 2000
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patientsA Poyau, K Buchet, M F Bouzidi, et al.
Journal of Medical Genetics|October 5, 2001
No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystoniaS Tuffery-Giraud, L Cavalier, A Roubertie, et al.
Journal of Pediatric Orthopedics|September 1, 1988
Skin elastic fiber pathology and idiopathic scoliosisB Echenne, G Barneon, M Pages, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 27, 2001
Retinal degeneration associated with congenital transcobalamin II deficiencyE H Souied, N Benhamou, M Sterkers, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Pageof 13

Showing results (91-100 of 121) with videos related to

Sort By:
Pageof 13
Revue Neurologique|May 2, 2002
[The varied etiologies of childhood-onset dystonia]A Roubertie, F Rivier, V Humbertclaude, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]V Humbertclaude, S Tourtet, M Semprino, et al.
Neurology|May 22, 1998
Congenital muscular dystrophy and cerebellar atrophyB Echenne, F Rivier, M Tardieu, et al.
Neuro-Chirurgie|August 17, 1999
[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case]P Coubes, B Echenne, A Roubertie, et al.
Annales De Pediatrie|May 1, 1984
[Chloramphenicol treatment of Haemophilus influenzae meningitis in the child]B Echenne, R Cheminal, F Rapin, et al.
Human Genetics|April 4, 2000
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patientsA Poyau, K Buchet, M F Bouzidi, et al.
Journal of Medical Genetics|October 5, 2001
No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystoniaS Tuffery-Giraud, L Cavalier, A Roubertie, et al.
Journal of Pediatric Orthopedics|September 1, 1988
Skin elastic fiber pathology and idiopathic scoliosisB Echenne, G Barneon, M Pages, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 27, 2001
Retinal degeneration associated with congenital transcobalamin II deficiencyE H Souied, N Benhamou, M Sterkers, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Pageof 13