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Results: 1-17 |
Results: 17
Mitochondrial neurogastrointestinal encephalopathy
Authors: Durant, R Labauge, P Yeche, S Castelnovo, G Reynaud, D Figarella-Branger, D Dubois, A
Citation: R. Durant et al., Mitochondrial neurogastrointestinal encephalopathy, REV MED IN, 22, 2001, pp. 230S-231S
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
Authors: Joutel, A Favrole, P Labauge, P Chabriat, H Lescoat, C Andreux, F Domenga, V Cecillon, M Vahedi, K Ducros, A Cave-Riant, F Bousser, MG Tournier-Lasserve, E
Citation: A. Joutel et al., Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis, LANCET, 358(9298), 2001, pp. 2049-2051
Familial form of cerebral cavernous malformations: evaluation of gradient-spin-echo (GRASE) imaging in lesion detection and characterization at 1.5 T
Authors: Brunereau, L Leveque, C Bertrand, P Tranquart, F Cordoliani, Y Rouleau, P Labauge, P
Citation: L. Brunereau et al., Familial form of cerebral cavernous malformations: evaluation of gradient-spin-echo (GRASE) imaging in lesion detection and characterization at 1.5 T, NEURORADIOL, 43(11), 2001, pp. 973-979
The prevalence of Sjogren syndrome in patients with primary progressive multiple sclerosis
Authors: de Seze, J Devos, D Castelnovo, G Labauge, P Dubucquoi, S Stojkovic, T Ferriby, D Vermersch, P
Citation: J. De Seze et al., The prevalence of Sjogren syndrome in patients with primary progressive multiple sclerosis, NEUROLOGY, 57(8), 2001, pp. 1359-1363
Prospective follow-up of 33 asymptomatic patients with familial cerebral cavernous malformations
Authors: Labauge, P Brunereau, L Laberge, S Houtteville, JP
Citation: P. Labauge et al., Prospective follow-up of 33 asymptomatic patients with familial cerebral cavernous malformations, NEUROLOGY, 57(10), 2001, pp. 1825-1828
Appearance of new lesions in two nonfamilial cerebral cavernoma patients
Authors: Labauge, P Brunereau, L Coubes, P Clanet, M Tannier, C Laberge, S Levy, C
Citation: P. Labauge et al., Appearance of new lesions in two nonfamilial cerebral cavernoma patients, EUR NEUROL, 45(2), 2001, pp. 83-88
Rapidly progressive dementia disclosing primary angiitis of the central nervous system
Authors: Castelnovo, G Bouly, S Vladut, M Marty-Double, C Labauge, P
Citation: G. Castelnovo et al., Rapidly progressive dementia disclosing primary angiitis of the central nervous system, ANN MED IN, 152(4), 2001, pp. 273-275
Cerebromeningeal bleeding after voluntary overdose of pseudoephedrine
Authors: LeBayon, A Castelnovo, G Briere, C Labauge, P
Citation: A. Lebayon et al., Cerebromeningeal bleeding after voluntary overdose of pseudoephedrine, PRESSE MED, 29(31), 2000, pp. 1702-1702
De novo lesions in familial form of cerebral cavernous malformations: Clinical and MR features in 29 non-hispanic families
Authors: Brunereau, L Levy, C Laberge, S Houtteville, JP Labauge, P
Citation: L. Brunereau et al., De novo lesions in familial form of cerebral cavernous malformations: Clinical and MR features in 29 non-hispanic families, SURG NEUROL, 53(5), 2000, pp. 475-482
Familial form of intracranial cavernous angioma: MR imaging findings in 51families
Authors: Brunereau, L Labauge, P Tournier-Lasserve, E Laberge, S Levy, C Houtteville, JP
Citation: L. Brunereau et al., Familial form of intracranial cavernous angioma: MR imaging findings in 51families, RADIOLOGY, 214(1), 2000, pp. 209-216
The natural history of familial cerebral cavernomas: a retrospective MRI study of 40 patients
Authors: Labauge, P Brunereau, L Levy, C Laberge, S Houtteville, JP
Citation: P. Labauge et al., The natural history of familial cerebral cavernomas: a retrospective MRI study of 40 patients, NEURORADIOL, 42(5), 2000, pp. 327-332
Isolated spastic paraparesis leading to diagnosis of Friedreich's ataxia
Authors: Castelnovo, G Biolsi, B Barbaud, A Labauge, P Schmitt, M
Citation: G. Castelnovo et al., Isolated spastic paraparesis leading to diagnosis of Friedreich's ataxia, J NE NE PSY, 69(5), 2000, pp. 693-693
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
Authors: Laberge-le Couteulx, S Jung, HH Labauge, P Houtteville, JP Lescoat, C Cecillon, M Marechal, E Joutel, A Bach, JF Tournier-Lasserve, E
Citation: S. Laberge-le Couteulx et al., Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas, NAT GENET, 23(2), 1999, pp. 189-193
Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families
Authors: Laberge, S Labauge, P Marechal, E Maciazek, J Tournier-Lasserve, E
Citation: S. Laberge et al., Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families, EUR J HUM G, 7(4), 1999, pp. 499-504
An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families
Authors: Labauge, P Enjolras, O Bonerandi, JJ Laberge, S Dandurand, M Joujoux, JM Tournier-Lasserve, E
Citation: P. Labauge et al., An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families, ANN NEUROL, 45(2), 1999, pp. 250-254
Spanish families with cavernous angiomas do not share the Hispano-AmericanCCM1 haplotype
Authors: Jung, HH Labauge, P Laberge, S Marechal, E Tournier-Lasserve, E Lucas, M Garcia-Moreno, JM Gamero, MA Izquierdo, G Tournier-Lasserve, E
Citation: Hh. Jung et al., Spanish families with cavernous angiomas do not share the Hispano-AmericanCCM1 haplotype, J NE NE PSY, 67(4), 1999, pp. 551-552
Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families
Authors: Labauge, P Laberge, S Brunereau, L Levy, C Tournier-Lasserve, E
Citation: P. Labauge et al., Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families, LANCET, 352(9144), 1998, pp. 1892-1897
Risultati: 1-17 |