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Results: 1-13 |
Results: 13
Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations
Authors: Vital, A Ferrer, X Lagueny, A Vandenberghe, A Latour, P Goizet, C Canron, MH Louiset, P Petry, KG Vital, C
Citation: A. Vital et al., Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations, J PERIPH N, 6(2), 2001, pp. 79-84
Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene
Authors: Lagueny, A Latour, P Vital, G Le Masson, G Rouanet, M Ferrer, X Vital, C Vandenberghe, A
Citation: A. Lagueny et al., Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene, J NE NE PSY, 70(2), 2001, pp. 232-235
Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth IA duplication
Authors: Latour, P Boutrand, L Levy, N Bernard, R Boyer, A Claustrat, F Chazot, G Boucherat, M Vandenberghe, A
Citation: P. Latour et al., Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth IA duplication, CLIN CHEM, 47(5), 2001, pp. 829-837
Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A
Authors: Rajabally, Y Vital, A Ferrer, X Vital, C Julien, J Latour, P Vandenberghe, A Lagueny, A
Citation: Y. Rajabally et al., Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A, J PERIPH N, 5(3), 2000, pp. 158-162
Hereditary neuropathy with liability to pressure palsies (HNPP) in a child: clinical and biological features
Authors: Lesca, G Meunier, S Zine, A Jeannoel, P Latour, P Vandenberghe, A
Citation: G. Lesca et al., Hereditary neuropathy with liability to pressure palsies (HNPP) in a child: clinical and biological features, ARCH PED, 7(3), 2000, pp. 271-273
Recurrent facial nerve palsy in a patient with hereditary neuropathy with liability to pressure palsy
Authors: Drouet, A Guilloton, L Latour, P Ribot, C
Citation: A. Drouet et al., Recurrent facial nerve palsy in a patient with hereditary neuropathy with liability to pressure palsy, PRESSE MED, 29(12), 2000, pp. 655-655
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
Authors: Morle, L Bozon, M Alloisio, N Latour, P Vandenberghe, A Plauchu, H Collet, L Edery, P Godet, J Lina-Granade, G
Citation: L. Morle et al., A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss, J MED GENET, 37(5), 2000, pp. 368-370
Asymmetrical polyneuropathy with a stepwise progressive course and well-demarcated areas of demyelination
Authors: Vital, A Barat, M Lagueny, A Latour, P Vital, C
Citation: A. Vital et al., Asymmetrical polyneuropathy with a stepwise progressive course and well-demarcated areas of demyelination, MUSCLE NERV, 22(8), 1999, pp. 1139-1145
Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q) (vol 52, pg 1010, 1999)
Authors: Stojkovic, T Latour, P Vandenberghe, A Hurtevant, JF Vermersch, P
Citation: T. Stojkovic et al., Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q) (vol 52, pg 1010, 1999), NEUROLOGY, 52(9), 1999, pp. 1952-1952
Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)
Authors: Stojkovic, T Latour, P Vandenberghe, A Hurtevent, JF Vermersch, P
Citation: T. Stojkovic et al., Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q), NEUROLOGY, 52(5), 1999, pp. 1010-1014
Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutationin the myelin protein zero gene
Authors: Chapon, F Latour, P Diraison, P Schaeffer, S Vandenberghe, A
Citation: F. Chapon et al., Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutationin the myelin protein zero gene, J NE NE PSY, 66(6), 1999, pp. 779-782
Alternative exon 3 splicing of the human major protein zero gene in white blood cells and peripheral nerve tissue
Authors: Besancon, R Prost, AL Konecny, L Latour, P Petiot, P Boutrand, L Kopp, N Mularoni, A Chamba, G Vandenberghe, A
Citation: R. Besancon et al., Alternative exon 3 splicing of the human major protein zero gene in white blood cells and peripheral nerve tissue, FEBS LETTER, 457(3), 1999, pp. 339-342
Incidence of inflammatory bowel disease in the area of Liege: A 3 years prospective study (1993-1996)
Authors: Latour, P Louis, E Belaiche, J
Citation: P. Latour et al., Incidence of inflammatory bowel disease in the area of Liege: A 3 years prospective study (1993-1996), ACT GASTR B, 61(4), 1998, pp. 410-413
Risultati: 1-13 |