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Results: 1-8 |
Results: 8
Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations.
Authors: Penisson-Besnier, I Moreau, C Jacques, C Roger, JC Dubas, F Reynier, P
Citation: I. Penisson-besnier et al., Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations., REV NEUROL, 157(5), 2001, pp. 537-541
Trismus, pseudobulbar syndrome and cerebral deep venous thrombosis.
Authors: Alecu, C de Bray, JM Penisson-Besnier, I Pasco-Papon, A Dubas, F
Citation: C. Alecu et al., Trismus, pseudobulbar syndrome and cerebral deep venous thrombosis., REV NEUROL, 157(3), 2001, pp. 309-314
Cervical artery dissections in the puerperium: Pathogenic hypotheses concerning seven observations
Authors: de Bray, JM Guillon, B Neau, JP Bouilliat, J Ducrocq, X Saudeau, D Vincent, D Penisson-Besnier, I Pasco, A Dubas, F
Citation: Jm. De Bray et al., Cervical artery dissections in the puerperium: Pathogenic hypotheses concerning seven observations, CEREB DIS, 10(2), 2000, pp. 158-159
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
Authors: Bonne, G Mercuri, E Muchir, A Urtizberea, A Becane, HM Recan, D Merlini, L Wehnert, M Boor, R Reuner, U Vorgerd, M Wicklein, EM Eymard, B Duboc, D Penisson-Besnier, I Cuisset, JM Ferrer, X Desguerre, I Lacombe, D Bushby, K Pollitt, C Toniolo, D Fardeau, M Schwartz, K Muntoni, F
Citation: G. Bonne et al., Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene, ANN NEUROL, 48(2), 2000, pp. 170-180
Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation
Authors: Penisson-Besnier, I Reynier, P Asfar, P Douay, O Sortais, A Dubas, F Emile, J Malthiery, Y
Citation: I. Penisson-besnier et al., Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation, NEUROLOGY, 55(2), 2000, pp. 317-318
mtDNA haplogroup J: a contributing factor of optic neuritis
Authors: Reynier, P Penisson-Besnier, I Moreau, C Savagner, F Vielle, B Emile, J Dubas, F Malthiery, Y
Citation: P. Reynier et al., mtDNA haplogroup J: a contributing factor of optic neuritis, EUR J HUM G, 7(3), 1999, pp. 404-406
Unusual skin reaction after intravenous infusion of polyvalent immunoglobulins - 3 observations
Authors: Leclech, C Maillard, H Penisson-Besnier, I Laine-Cessac, P Verret, JL
Citation: C. Leclech et al., Unusual skin reaction after intravenous infusion of polyvalent immunoglobulins - 3 observations, PRESSE MED, 28(10), 1999, pp. 531-531
Peripheral motor deficit and three vertebral artery dissections.
Authors: de Bray, JM Penisson-Besnier, I Giroud, M Klein, J Tanguy, K Pasco, A Dubas, F
Citation: Jm. De Bray et al., Peripheral motor deficit and three vertebral artery dissections., REV NEUROL, 154(11), 1998, pp. 762-766
Risultati: 1-8 |