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Results: 1-17 |
Results: 17
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
Neurological complications linked to antalgesics and anti-inflammatory agents
Authors: Chabrol, B Mely, L Lethel, V Hugonenc, C Dubus, JC Mancini, J
Citation: B. Chabrol et al., Neurological complications linked to antalgesics and anti-inflammatory agents, ARCH PED, 8, 2001, pp. 329S-331S
Mevalonic aciduria and hyper-IgD syndrome: Two sides of the same coin?
Authors: Tsimaratos, M Kone-Paut, I Divry, P Philip, N Chabrol, B
Citation: M. Tsimaratos et al., Mevalonic aciduria and hyper-IgD syndrome: Two sides of the same coin?, J INH MET D, 24(3), 2001, pp. 413-414
A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases
Authors: de Lonlay, P Seta, N Barrot, S Chabrol, B Drouin, V Gabriel, BM Journel, H Kretz, M Laurent, J Le Merrer, M Leroy, A Pedespan, D Sarda, P Villeneuve, N Schmitz, J van Schaftingen, E Matthijs, G Jaeken, J Korner, C Munnich, A Saudubray, JM Cormier-Daire, V
Citation: P. De Lonlay et al., A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases, J MED GENET, 38(1), 2001, pp. 14-19
Brain injuries in early foetal life: consequences for brain development
Authors: Mancini, J Lethel, V Hugonenq, C Chabrol, B
Citation: J. Mancini et al., Brain injuries in early foetal life: consequences for brain development, DEVELOP MED, 43(1), 2001, pp. 52-55
Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28
Authors: Villard, L des Portes, V Levy, N Louboutin, JP Recan, D Coquet, M Chabrol, B Figarella-Branger, D Chelly, J Pellissier, JF Fontes, M
Citation: L. Villard et al., Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28, EUR J HUM G, 8(2), 2000, pp. 125-129
Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
Authors: Chandler, D Angelicheva, D Heather, L Gooding, R Gresham, D Yanakiev, P de Jonge, R Baas, F Dye, D Karagyozov, L Savov, A Blechschmidt, K Keats, B Thomas, PK King, RHM Starr, A Nikolova, A Colomer, J Ishpekova, B Tournev, I Urtizberea, JA Merlini, L Butinar, D Chabrol, B Voit, T Baethmann, M Nedkova, V Corches, A Kalaydjieva, L
Citation: D. Chandler et al., Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries, NEUROMUSC D, 10(8), 2000, pp. 584-591
Chronic renal failure and portal hypertension - is portosystemic shunt indicated?
Authors: Tsimaratos, M Cloarec, S Roquelaure, B Retornaz, K Picon, G Chabrol, B Guys, JM Sarles, J Nivet, H
Citation: M. Tsimaratos et al., Chronic renal failure and portal hypertension - is portosystemic shunt indicated?, PED NEPHROL, 14(8-9), 2000, pp. 856-858
Lamotrigine therapy in children: retrospective study of 32 patients.
Authors: Lethel, V Chabrol, B Livet, MO Mancini, J
Citation: V. Lethel et al., Lamotrigine therapy in children: retrospective study of 32 patients., ARCH PED, 7(3), 2000, pp. 234-242
Circulating endothelial cells in Behcet's disease with cerebral thrombophlebitis
Authors: Camoin-Jau, L Kone-Paut, I Chabrol, B Sampol, J Dignat-George, F
Citation: L. Camoin-jau et al., Circulating endothelial cells in Behcet's disease with cerebral thrombophlebitis, THROMB HAEM, 83(4), 2000, pp. 631-632
Pseudometabolic dystrophinopathy without immunohistochemical anomaly
Authors: Serratrice, J Chabrol, B Attarrian, S Figarella-Branger, D
Citation: J. Serratrice et al., Pseudometabolic dystrophinopathy without immunohistochemical anomaly, REV NEUROL, 156(2), 2000, pp. 175-178
Brain metabolic impairment in non-cerebral and cerebral forms of X-linked adrenoleukodystrophy by proton MRS: Identification of metabolic patterns bydiscriminant analysis
Authors: Salvan, AM Confort-Gouny, S Chabrol, B Cozzone, PJ Vion-Dury, J
Citation: Am. Salvan et al., Brain metabolic impairment in non-cerebral and cerebral forms of X-linked adrenoleukodystrophy by proton MRS: Identification of metabolic patterns bydiscriminant analysis, MAGN RES M, 41(6), 1999, pp. 1119-1126
In vivo brain proton MR spectroscopy in a case of molybdenum cofactor deficiency
Authors: Salvan, AM Chabrol, B Lamoureux, S Confort-Gouny, S Cozzone, PJ Vion-Dury, J
Citation: Am. Salvan et al., In vivo brain proton MR spectroscopy in a case of molybdenum cofactor deficiency, PEDIAT RAD, 29(11), 1999, pp. 846-848
The role of cranial MRI in identifying patients suffering from child abuseand presenting with unexplained neurological findings
Authors: Chabrol, B Decarie, JC Fortin, G
Citation: B. Chabrol et al., The role of cranial MRI in identifying patients suffering from child abuseand presenting with unexplained neurological findings, CHILD ABUSE, 23(3), 1999, pp. 217-228
Clinical approach to gene-dependant mental deficiencies.
Authors: Livet, NO Moncla, A Philip, N Chabrol, B Mancini, J
Citation: No. Livet et al., Clinical approach to gene-dependant mental deficiencies., REV NEUROL, 155(8), 1999, pp. 593-595
In vivo cerebral proton MRS in a case of subacute sclerosing panencephalitis
Authors: Salvan, AM Confort-Gouny, S Cozzone, PJ Vion-Dury, J Chabrol, B Mancini, J
Citation: Am. Salvan et al., In vivo cerebral proton MRS in a case of subacute sclerosing panencephalitis, J NE NE PSY, 66(4), 1999, pp. 547-548
Child abuse and neglect in Quebec: program of the child protection clinic of Sainte-Justine Hospital, Montreal
Authors: Chabrol, B Fortin, G Bernard-Bonnin, AC Allard-Dansereau, C Chabot, G Methot, B
Citation: B. Chabrol et al., Child abuse and neglect in Quebec: program of the child protection clinic of Sainte-Justine Hospital, Montreal, ARCH PED, 5(12), 1998, pp. 1366-1370
Risultati: 1-17 |