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Results: 1-6 |
Results: 6

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

Authors: Pradat-Diehl, P Tessier, C Vallat, C Mailhan, L Mazevet, D Lauriot-Prevost, MC Bergego, C
Citation: P. Pradat-diehl et al., Conduction aphasia and phonemic disorder, REV NEUROL, 157(10), 2001, pp. 1245-1252

Authors: Dereure, O Aguilar-Martinez, P Bessis, D Perney, P Vallat, C Guillot, B Blanc, F Guilhou, JJ
Citation: O. Dereure et al., HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France, BR J DERM, 144(3), 2001, pp. 533-539

Authors: Vallat, C Bellet, H Faucherre, V Bessis, D Callis, A Brunel, M Guilhou, JJ
Citation: C. Vallat et al., Curing of a cutaneous porphyria in a patient infected with human immunodeficiency virus treated by tritherapy, REV MED IN, 21(3), 2000, pp. 299-300

Authors: Bellet, H Rejou, F Vallat, C Mion, H Dimeglio, A
Citation: H. Bellet et al., Cystinylglycinuria: A new neurometabolic disorder?, J INH MET D, 22(3), 1999, pp. 231-234

Authors: Pradat-Diehl, P Masure, MC Lauriot-Prevost, MC Vallat, C Bergego, C
Citation: P. Pradat-diehl et al., Impairment of visual recognition after a traumatic brain injury, REV NEUROL, 155(5), 1999, pp. 375-382
Risultati: 1-6 |