AAAAAA

   
Results: 1-10 |
Results: 10
Acute transverse myelitis in the child of uncommon etiology: the lymphocytic choriomeningitis virus.
Authors: Humbertclaude, V Tourtet, S Semprino, M Roubertie, A Rivier, F Leboucq, N Astruc, J Echenne, B
Citation: V. Humbertclaude et al., Acute transverse myelitis in the child of uncommon etiology: the lymphocytic choriomeningitis virus., ARCH PED, 8(3), 2001, pp. 282-285
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance
Authors: Humbertclaude, V Rivier, F Roubertie, A Echenne, B Bellet, H Vallat, C Morin, D
Citation: V. Humbertclaude et al., Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance, J CHILD NEU, 16(8), 2001, pp. 622-623
Treatment of early-onset dystonia: update and a new perspective
Authors: Roubertie, A Echenne, B Cif, L Vayssiere, N Hemm, S Coubes, P
Citation: A. Roubertie et al., Treatment of early-onset dystonia: update and a new perspective, CHILD NERV, 16(6), 2000, pp. 334-340
Treatment of DYT1-generalised dystonia by stimulation of the internal globus pallidus
Authors: Coubes, P Roubertie, A Vayssiere, N Hemm, S Echenne, B
Citation: P. Coubes et al., Treatment of DYT1-generalised dystonia by stimulation of the internal globus pallidus, LANCET, 355(9222), 2000, pp. 2220-2221
Ring chromosome 20 and epilepsy: a recognizable syndrome (two new cases)
Authors: Roubertie, A Petit, J Genton, P
Citation: A. Roubertie et al., Ring chromosome 20 and epilepsy: a recognizable syndrome (two new cases), REV NEUROL, 156(2), 2000, pp. 149-153
Non-convulsive status in the ring chromosome 20 syndrome: a video illustration of 3 cases
Authors: Petit, J Roubertie, A Inoue, Y Genton, P
Citation: J. Petit et al., Non-convulsive status in the ring chromosome 20 syndrome: a video illustration of 3 cases, EPILEPT DIS, 1(4), 1999, pp. 237-241
Benign familial infantile convulsions.
Authors: Echenne, B Rivier, F Humbertclaude, V Roubertie, A Cheminal, R Malafosse, A
Citation: B. Echenne et al., Benign familial infantile convulsions., ARCH PED, 6(1), 1999, pp. 54-58
Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1
Authors: Echenne, B Ducros, A Rivier, F Joutel, A Humbertclaude, V Roubertie, A Azais, M Bousser, MG Tournier-Lasserve, E
Citation: B. Echenne et al., Recurrent episodes of coma: An unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1, NEUROPEDIAT, 30(4), 1999, pp. 214-217
Treatment of early-onset generalized dystonia by bilateral chronic electrical stimulation of the internal globus pallidus. Case report.
Authors: Coubes, P Echenne, B Roubertie, A Vayssiere, N Tuffery, S Humbertclaude, V Cambonie, G Claustres, M Frerebeau, P
Citation: P. Coubes et al., Treatment of early-onset generalized dystonia by bilateral chronic electrical stimulation of the internal globus pallidus. Case report., NEUROCHIRE, 45(2), 1999, pp. 139-144
Vigabatrin-associated retinal cone system dysfunction
Authors: Roubertie, A Bellet, H Echenne, B
Citation: A. Roubertie et al., Vigabatrin-associated retinal cone system dysfunction, NEUROLOGY, 51(6), 1998, pp. 1779-1779
Risultati: 1-10 |