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Results:
1-22
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Results: 22
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
Authors:
Boutrand, L
Egyed, B
Furedi, S
Mommers, N
Mertens, G
Vandenberghe, A
Citation: L. Boutrand et al., Variations in primer sequences are the origin of allele drop-out at loci D13S317 and CD4, INT J LEGAL, 114(4-5), 2001, pp. 295-297
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
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
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
Authors:
Egyed, B
Furedi, S
Angyal, M
Boutrand, L
Vandenberghe, A
Woller, J
Padar, Z
Citation: B. Egyed et al., Analysis of eight STR loci in two Hungarian populations, INT J LEGAL, 113(5), 2000, pp. 272-275
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
Authors:
Egyed, B
Furedi, S
Angyal, M
Boutrand, L
Vandenberghe, A
Woller, J
Padar, Z
Citation: B. Egyed et al., Analysis of eight STR loci in two Hungarian populations, FOREN SCI I, 113(1-3), 2000, pp. 25-27
Authors:
Vallat, JM
Tabaraud, F
Sindou, P
Preux, PM
Vandenberghe, A
Steck, A
Citation: Jm. Vallat et al., Myelin widenings and MGUS-IgA: An immunoelectron microscopic study, ANN NEUROL, 47(6), 2000, pp. 808-811
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
Authors:
Bissar-Tadmouri, N
Parman, Y
Boutrand, L
Deymeer, F
Serdaroglu, P
Vandenberghe, A
Battaloglu, E
Citation: N. Bissar-tadmouri et al., Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type I and HNPP patients, CLIN GENET, 58(5), 2000, pp. 396-402
Authors:
Lopes, J
Tardieu, S
Silander, K
Blair, I
Vandenberghe, A
Palau, F
Ruberg, M
Brice, A
LeGuern, E
Citation: J. Lopes et al., Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP, HUM MOL GEN, 8(12), 1999, pp. 2285-2292
Authors:
Mertens, G
Gielis, M
Mommers, N
Mularoni, A
Lamartine, J
Heylen, H
Muylle, L
Vandenberghe, A
Citation: G. Mertens et al., Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles, INT J LEGAL, 112(3), 1999, pp. 192-194
Authors:
Bost, M
Lachaux, A
Accominotti, M
Vandenberghe, A
Citation: M. Bost et al., Mutation screening and genotype-phenotype correlation in 32 families with Wilson disease, J TR EL EXP, 12(4), 1999, pp. 321-329
Authors:
Tabaraud, F
Lagrange, E
Sindou, P
Vandenberghe, A
Levy, N
Vallat, JM
Citation: F. Tabaraud et al., Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings, MUSCLE NERV, 22(10), 1999, pp. 1442-1447
Authors:
Sindou, P
Vallat, JM
Chapon, F
Archelos, JJ
Tabaraud, F
Anani, T
Braund, KG
Maisonobe, T
Hauw, JJ
Vandenberghe, A
Citation: P. Sindou et al., Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease, MUSCLE NERV, 22(1), 1999, pp. 99-104
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
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
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
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
Authors:
Duthel, S
Bost, M
Ollagnon, E
Vial, C
Petiot, P
Chazot, G
Vandenberghe, A
Citation: S. Duthel et al., CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbers, ANN GENET, 42(3), 1999, pp. 151-159
Authors:
Bouhouche, A
Benomar, A
Birouk, N
Mularoni, A
Meggouh, F
Tassin, J
Grid, D
Vandenberghe, A
Yahyaoui, M
Chkili, T
Brice, A
LeGuern, E
Citation: A. Bouhouche et al., A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2q21.3, AM J HU GEN, 65(3), 1999, pp. 722-727
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