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Results: 1-13 |
Results: 13
Prenatal diagnosis of schizencephaly by fetal magnetic resonance imaging
Authors: Denis, D Maugey-Laulom, B Carles, D Pedespan, JM Brun, M Chateil, JF
Citation: D. Denis et al., Prenatal diagnosis of schizencephaly by fetal magnetic resonance imaging, FETAL DIAGN, 16(6), 2001, pp. 354-359
X-linked myopathy with excessive autophagy: a clinicopathological study offive new families
Authors: Chabrol, B Figarella-Branger, D Coquet, M Mancini, J Fontan, D Pedespan, JM Francannet, C Pouget, J Beaufrere, AM Pellilssier, JF
Citation: B. Chabrol et al., X-linked myopathy with excessive autophagy: a clinicopathological study offive new families, NEUROMUSC D, 11(4), 2001, pp. 376-388
Multiple sclerosis: pathogenesis and clinical modalities of onset in children.
Authors: Brissaud, O Palin, K Chateil, JF Pedespan, JM
Citation: O. Brissaud et al., Multiple sclerosis: pathogenesis and clinical modalities of onset in children., ARCH PED, 8(9), 2001, pp. 969-978
Cerebellar vermis hypoplasias with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes
Authors: Graber, D Antignac, C Deschenes, G Coulin, A Hermouet, Y Pedespan, JM Fontan, D Ponsot, G
Citation: D. Graber et al., Cerebellar vermis hypoplasias with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes, ARCH PED, 8(2), 2001, pp. 186-190
Interferon-beta treatment in patients with childhood onset multiple sclerosis
Authors: Mikaelloff, Y Moreau, T Debouverie, M Pelletier, J Lebrun, C Gout, O Pedespan, JM Van Hulle, C Vermersch, P Ponsot, G
Citation: Y. Mikaelloff et al., Interferon-beta treatment in patients with childhood onset multiple sclerosis, J PEDIAT, 139(3), 2001, pp. 443-446
MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis
Authors: Chateil, JF Soussotte, C Pedespan, JM Brun, M Le Manh, C Diard, F
Citation: Jf. Chateil et al., MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis, BR J RADIOL, 74(877), 2001, pp. 24-31
Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation
Authors: Rodriguez, D Gauthier, F Bertini, E Bugiani, M Brenner, M N'guyen, S Goizet, C Gelot, A Surtees, R Pedespan, JM Hernandorena, X Troncoso, M Uziel, G Messing, A Ponsot, G Pham-Dinh, D Dautigny, A Boespflug-Tanguy, O
Citation: D. Rodriguez et al., Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation, AM J HU GEN, 69(5), 2001, pp. 1134-1140
Schizencephaly: clinical and imaging features in 30 infantile cases
Authors: Denis, D Chateil, JF Brun, M Brissaud, O Lacombe, D Fontan, D Flurin, V Pedespan, JM
Citation: D. Denis et al., Schizencephaly: clinical and imaging features in 30 infantile cases, BRAIN DEVEL, 22(8), 2000, pp. 475-483
Epilepsies and time to diagnosis
Authors: Cachera, C Baulac, M Fagnani, F Jallon, P Leveau, J Loiseau, P Motte, J Thomas, P Vallee, L Allaire, C Autret, A Baldy-Moulinier, M Clanet, M Dordain, G Gastaut, JL Giroud, M Josien, E Marescaux, C Masnou, P Mauguiere, F Parain, D Perret, J Revol, M Rumbach, L Tapie, P Weber, M Adam, C Attal, N Attane, F Aubrun, P Ayrivie, N Badinand-Hubert, N Bapst-Reiter, J Barthez-Carpentier, MA Bartolomei, F Bataillard, M Bednarek, N Belair, C Benazet, M Berges, S Bergouignan, FX Bernard, C Bernard-Bourzeix, L Bertran, F Bertrand, P Beuriat, P Billard, C Bille-Turc, F Billy, C Biraben, A Blanc, A Boidein, F Bouayed, N Boudon, S Bouillat, J Boulloche, J Bredin, A Brocard, O Brosset, P Brunet-Bourgin, F Cenraud, B Chaigne, D Chaix, Y Chaunu, MP Chavot, D Clavelou, P Cohadon, S Collombier, N Contis, PE Convers, P Couchot, J Cournelle, MA Courtois, S Croguennec, JM Cuisset, JM Cuvellier, JC d'Anglejan, J Damon, G Danielli, A Daubney, P de Bellescize, J de Lumley, L de Recondo, A de Swarte, M Deffond, D Delangre, T Delisse, B Derambure, P Derambure, S Desbordes, P Desfrancois, F Destee-Warot, M Dien, J Doremus, B Dourneau-Lethiecq, MC Dubois, F Duche, B Ducrocq, X Duhurt, J Duprey, J Durand, G Dusser, A Escaillas, JP Fanjaud, G Felten, D Fischer, C Fontan, D Formosa, F Foulon, E Furby, A Gallet, S Galmiche, J Garde-Arthaud, P Garrel, S Gaultier, C Gauthier, C Gauthier-Morel, D Genton, P Geraud, G Girard, JP Girard-Madoux, M Gonnaud, P Goulon-Goeau, C Gros, S Grosclaude, M Gross, M Gueguen, B Guinot, H Haenggeli, CA Hamon, JB Henlin, JL Hevin, B Hinault, P Homeyer, P Hommet, C Huart, E Huc, P Huttin, B Inglesiakis, L Isnard, J Isnard, H Jogeix, M Juhel, C Kahane, P Kalafat, M Keo-Kosal, P Kreib, AM Kubler, C Larrieu, E Larrieu, JL Latinville, D Le Gallou-Wittenberg, A Lebas, F Lebrun-Grandie, P Leche, J Legout, A Legrand, S Legroux, M Lemaitre, JF Lestavel, P Levasseur, M Lienhard, C Livet, MO Louiset, P Lubeau, M Lucas, B Lucas-Daviaud, J Maillard, S Maillet-Vioud, M Mancini, J Mann, M Marchal, C Martini, L Maupetit, J Maynard, R Menage, P Menard, D Metreau, R Milor, M Minot-Myhie, MC Moene, Y Montagne, B Montelescaut, ME Moreaud, O Noelle, B Olmi, X Orbegozo, J Ouvrard-Hernandez, AM Parsa, A Pautrizel, B Pedespan, JM Pernes, P Perrouty, B Petit, J Peudenier, S Picard, AM Pierrot-Deseilligny, C Planque, E Portha, C Preux, PM Prud'homme, M Raybaut-Guilhem, D Rebaud, P Regi, A Regi, JL Reis, J Rejou, F Remy, C Renard, JF Revenu, M Revol, A Rey, M Richelme, C Ricou, P Rigal, JP Rogez, R Rousselle, C Rummens, C Ryvlin, P Sabouraud, P Saikali, I Saudeau, D Savet, JF Schaeffer, JL Schaff, JL SCHoenfelder, F Schuermans, P Senant, J Setiey, A Sevrin, C Sivelle, G Soisson, T Soubielle, P Soulages, X Soulayrol, S Tabaraud, F Taillandier, P Tannier, C Tarel, V Taussig, D Thedrez, F Tournier, CL Turc, JD Vanhulle, C Vaunaize, J Verier, A Vernay, D Visy, JM Vongsouthi, C Vrigneaud, J Waubant, E Weichlein, A Weill, O Zai, L Ziegler, F Zix, C de Zelicourt, M
Citation: C. Cachera et al., Epilepsies and time to diagnosis, REV NEUROL, 156(5), 2000, pp. 481-490
Statistical analysis of mitochondrial pathologies in childhood: Identification of deficiencies using principal component analysis
Authors: Letellier, T Durrieu, G Malgat, M Rossignol, R Antoch, J Deshouillers, JM Coquet, M Lacombe, D Netter, JC Pedespan, JM Redonnet-Vernhet, I Mazat, JP
Citation: T. Letellier et al., Statistical analysis of mitochondrial pathologies in childhood: Identification of deficiencies using principal component analysis, LAB INV, 80(7), 2000, pp. 1019-1030
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases
Authors: Leuzzi, V Lyon, G Cilio, MR Pedespan, JM Fontan, D Chateil, JF Vital, A
Citation: V. Leuzzi et al., Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases, J NE NE PSY, 66(3), 1999, pp. 407-408
Cortical resections in children.
Authors: Rougier, A Pedespan, JM Loiseau, H Lurton, D Vital, A
Citation: A. Rougier et al., Cortical resections in children., DRUG-RESISTANT SEVERE PARTIAL EPILEPSY IN CHILDREN: DIAGNOSTIC STRATEGIES AND SURGICAL TREATMENTS, 1998, pp. 227-230
Indications and results of callosotomy in children.
Authors: Rougier, A Pedespan, JM Marchal, C Loiseau, P
Citation: A. Rougier et al., Indications and results of callosotomy in children., DRUG-RESISTANT SEVERE PARTIAL EPILEPSY IN CHILDREN: DIAGNOSTIC STRATEGIES AND SURGICAL TREATMENTS, 1998, pp. 236-240
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