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B Echenne

Showing results (101-110 of 121) with videos related to

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Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Annals of Neurology|April 1, 1994
Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions geneA Malafosse, C Beck, H Bellet, et al.
Human Molecular Genetics|March 1, 1997
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19qM Guipponi, F Rivier, F Vigevano, et al.
Brain & Development|September 1, 1991
Treatment of infantile spasms with intravenous gamma-globulinsB Echenne, O Dulac, M J Parayre-Chanez, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 12, 1999
[Benign infantile convulsions. French collaborative study]A Gautier, F Pouplard, N Bednarek, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Journal of the Neurological Sciences|August 1, 1986
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie InfantileB Echenne, M Arthuis, C Billard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2011
[Genetic syndromes that mimic congenital infections: report of 2 cases]M Thibault, J Leydet, E Tournier-Lasserve, et al.
Clinical Genetics|March 28, 2012
MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathiesL Lambert, T Bienvenu, L Allou, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 13
Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Annals of Neurology|April 1, 1994
Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions geneA Malafosse, C Beck, H Bellet, et al.
Human Molecular Genetics|March 1, 1997
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19qM Guipponi, F Rivier, F Vigevano, et al.
Brain & Development|September 1, 1991
Treatment of infantile spasms with intravenous gamma-globulinsB Echenne, O Dulac, M J Parayre-Chanez, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 12, 1999
[Benign infantile convulsions. French collaborative study]A Gautier, F Pouplard, N Bednarek, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Journal of the Neurological Sciences|August 1, 1986
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie InfantileB Echenne, M Arthuis, C Billard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2011
[Genetic syndromes that mimic congenital infections: report of 2 cases]M Thibault, J Leydet, E Tournier-Lasserve, et al.
Clinical Genetics|March 28, 2012
MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathiesL Lambert, T Bienvenu, L Allou, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Pageof 13