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B Echenne

Showing results (71-80 of 121) with videos related to

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Neuromuscular Disorders : NMD|May 1, 1997
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matterB Echenne, F Rivier, A J Jellali, et al.
Pediatrie|October 1, 1982
[Type II fucosidosis. 2 cases]B Echenne, P Baldet, I Maire, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|December 1, 1981
[All-night polygraphic recordings in the child with suspected epileptic seizures, in spite of normal routine and post-sleep deprivation EEGs (author's transl)]M Billiard, B Echenne, A Besset, et al.
Muscle & Nerve|September 15, 1998
Mosaic expression of two dystrophins in a boy with progressive muscular dystrophyF Rivier, S Tuffery, A J Jellali, et al.
Journal of Child Neurology|August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intoleranceV Humbertclaude, F Rivier, A Roubertie, et al.
Pediatrie|January 1, 1976
[Nosologic problems of essential polycythemia in children. Apropos of a case]B Echenne, D Brunel, J Astruc, et al.
Epilepsia|August 1, 1996
Treatment with vigabatrin may mimic alpha-aminoadipic aciduriaC Vallat, F Rivier, H Bellet, et al.
Neuromuscular Disorders : NMD|March 21, 2001
A standardized method for the evaluation of respiratory muscle endurance in patients with Duchenne muscular dystrophyS Matecki, N Topin, M Hayot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 14, 2003
[Movement disorders in childhood: classification and genetic update]A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Revue Neurologique|January 29, 2005
[Parry-Romberg's syndrome and epilepsy]M Chbicheb, A Gelot, F Rivier, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Neuromuscular Disorders : NMD|May 1, 1997
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matterB Echenne, F Rivier, A J Jellali, et al.
Pediatrie|October 1, 1982
[Type II fucosidosis. 2 cases]B Echenne, P Baldet, I Maire, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|December 1, 1981
[All-night polygraphic recordings in the child with suspected epileptic seizures, in spite of normal routine and post-sleep deprivation EEGs (author's transl)]M Billiard, B Echenne, A Besset, et al.
Muscle & Nerve|September 15, 1998
Mosaic expression of two dystrophins in a boy with progressive muscular dystrophyF Rivier, S Tuffery, A J Jellali, et al.
Journal of Child Neurology|August 21, 2001
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intoleranceV Humbertclaude, F Rivier, A Roubertie, et al.
Pediatrie|January 1, 1976
[Nosologic problems of essential polycythemia in children. Apropos of a case]B Echenne, D Brunel, J Astruc, et al.
Epilepsia|August 1, 1996
Treatment with vigabatrin may mimic alpha-aminoadipic aciduriaC Vallat, F Rivier, H Bellet, et al.
Neuromuscular Disorders : NMD|March 21, 2001
A standardized method for the evaluation of respiratory muscle endurance in patients with Duchenne muscular dystrophyS Matecki, N Topin, M Hayot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 14, 2003
[Movement disorders in childhood: classification and genetic update]A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Revue Neurologique|January 29, 2005
[Parry-Romberg's syndrome and epilepsy]M Chbicheb, A Gelot, F Rivier, et al.
Pageof 13