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Results:
1-23
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Results: 23
Authors:
Tubridy, N
Fontaine, B
Eymard, B
Citation: N. Tubridy et al., Congenital myopathies and congenital muscular dystrophies, CURR OP NEU, 14(5), 2001, pp. 575-582
Authors:
Bassez, G
Attarian, S
Laforet, P
Azulay, JP
Rouche, A
Ferrer, X
Urtizberea, JA
Pellissier, JF
Duboc, D
Fardeau, M
Pouget, J
Eymard, B
Citation: G. Bassez et al., Proximal myotonial myopathy (PROMM): clinical and histology study., REV NEUROL, 157(2), 2001, pp. 209-218
Authors:
Giraud, M
Beaurain, G
Yamamoto, AM
Eymard, B
Tranchant, C
Gajdos, P
Garchon, HJ
Citation: M. Giraud et al., Linkage of HLA to myasthenia gravis and genetic heterogeneity depending onanti-titin antibodies, NEUROLOGY, 57(9), 2001, pp. 1555-1560
Authors:
Laforet, P
Eymard, B
Fardeau, M
Caillaud, C
Nicolino, M
Poenaru, L
Citation: P. Laforet et al., Juvenile and adult-onset acid maltase deficiency in France: Genotype-phenotype correlation - Reply, NEUROLOGY, 57(10), 2001, pp. 1938-1938
Authors:
Hogrel, JY
Laforet, P
Ben Yaou, R
Chevrot, M
Eymard, B
Lombes, A
Citation: Jy. Hogrel et al., A non-ischemic forearm exercise test for the screening of patients with exercise intolerance, NEUROLOGY, 56(12), 2001, pp. 1733-1738
Authors:
Sternberg, D
Chatzoglou, E
Laforet, P
Fayet, G
Jardel, C
Blondy, P
Fardeau, M
Amselem, S
Eymard, B
Lombes, A
Citation: D. Sternberg et al., Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders, BRAIN, 124, 2001, pp. 984-994
Authors:
Yamamoto, AM
Gajdos, P
Eymard, B
Tranchant, C
Warter, JM
Gomez, L
Bourquin, C
Bach, JF
Garchon, HJ
Citation: Am. Yamamoto et al., Anti-titin antibodies in myasthenia gravis - Tight association with thymoma and heterogeneity of nonthymoma patients, ARCH NEUROL, 58(6), 2001, pp. 885-890
Authors:
Denier, C
Ducros, A
Durr, A
Eymard, B
Chassande, B
Tournier-Lasserve, E
Citation: C. Denier et al., Missense CACNA1A mutation causing episodic ataxia type 2, ARCH NEUROL, 58(2), 2001, pp. 292-295
Authors:
Cherin, P
Laforet, P
Gherardi, RK
Authier, FJ
Maisonobe, T
Coquet, M
Mussini, JM
Pellissier, JF
Eymard, B
Herson, S
Citation: P. Cherin et al., Macrophagic myofasciitis, PRESSE MED, 29(4), 2000, pp. 203-208
Authors:
Bonne, G
Mercuri, E
Muchir, A
Urtizberea, A
Becane, HM
Recan, D
Merlini, L
Wehnert, M
Boor, R
Reuner, U
Vorgerd, M
Wicklein, EM
Eymard, B
Duboc, D
Penisson-Besnier, I
Cuisset, JM
Ferrer, X
Desguerre, I
Lacombe, D
Bushby, K
Pollitt, C
Toniolo, D
Fardeau, M
Schwartz, K
Muntoni, F
Citation: G. Bonne et al., Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene, ANN NEUROL, 48(2), 2000, pp. 170-180
Authors:
Becane, HM
Bonne, G
Varnous, S
Muchir, A
Ortega, V
Hammouda, E
Urtizberea, JA
Lavergne, T
Fardeau, M
Eymard, B
Weber, S
Schwartz, K
Duboc, D
Citation: Hm. Becane et al., High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation, PACE, 23(11), 2000, pp. 1661-1666
Authors:
Fardeau, M
Vicart, P
Caron, A
Chateau, D
Chevallay, M
Collin, H
Chapon, F
Duboc, D
Eymard, B
Tome, FMS
Dupret, JM
Paulin, D
Guicheney, P
Citation: M. Fardeau et al., Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene, REV NEUROL, 156(5), 2000, pp. 497-504
Authors:
Eymard, B
Laforet, P
Tome, FMS
Collin, H
Leroy, JP
Hauw, JJ
Richard, I
Beckmann, J
Fardeau, M
Citation: B. Eymard et al., Miyoshi distal myopathy: specific signs and incidence., REV NEUROL, 156(2), 2000, pp. 161-168
Authors:
Laforet, P
Ziegler, F
Sternberg, D
Rouche, A
Frachon, P
Fardeau, M
Eymard, B
Lombes, A
Citation: P. Laforet et al., MELAS (A3243G) mutation of mitochondrial DNA: a study of the relationshipsbetween the clinical phenotype in 19 patients and morphological and molecular data., REV NEUROL, 156(12), 2000, pp. 1136-1147
Authors:
Navarro, V
Fournier, E
Girard, S
Delattre, JY
Eymard, B
Citation: V. Navarro et al., Hypokaliemic periodic paralysis disclosing Grave's disease: clinical and electrophysiological study, REV NEUROL, 156(1), 2000, pp. 59-61
Authors:
Laforet, P
Nicolino, M
Eymard, B
Puech, JP
Caillaud, C
Poenaru, L
Fardeau, M
Citation: P. Laforet et al., Juvenile and adult-onset acid maltase deficiency in France - Genotype-phenotype correlation, NEUROLOGY, 55(8), 2000, pp. 1122-1128
Authors:
Gonzalez, I
Ohsawa, N
Singer, RH
Devillers, M
Ashizawa, T
Balasubramanyam, A
Cooper, TA
Khajavi, M
Lia-Baldini, AS
Miller, G
Philips, AV
Timchenko, LT
Waring, J
Yamagata, H
Barbet, JP
Klesert, TR
Tapscott, SJ
Roses, AD
Wagner, M
Baiget, M
Martorell, L
Browne, GB
Eymard, B
Gourdon, G
Junien, C
Seznec, H
Carey, N
Gosling, M
Maire, P
Gennarelli, M
Sato, S
Ansved, T
Kvist, U
Eriksson, M
Furling, D
Chen, EJ
Housman, DE
Luciano, B
Siciliano, M
Spring, N
Shimizu, M
Eddy, E
Morris, GE
Krahe, R
Furuya, H
Adelman, J
Pribnow, D
Furutama, D
Mathieu, J
Hilton-Jones, D
Kinoshita, M
Abbruzzese, C
Sinden, RR
Wells, RD
Pearson, CE
Kobayashi, T
Johansson, A
Salvatori, S
Perryman, B
Swanson, MS
Gould, FK
Harris, SE
Johnson, K
Mitchell, AM
Monckton, DG
Winchester, CL
Antonini, G
Day, JW
Liquori, C
Ranum, LPW
Westerlaken, J
Wieringa, B
Griffith, JD
Michalowski, S
Moore, H
Hamshere, M
Korade, Z
Thornton, CA
Jaeger, H
Lehmann, F
Moorman, JR
Mounsey, JP
Mahadevan, MS
Citation: I. Gonzalez et al., New nomenclature and DNA testing guidelines for myotonic dystrophy type 1(DM1), NEUROLOGY, 54(6), 2000, pp. 1218-1221
Authors:
Lazarus, A
Varin, J
Ounnoughene, Z
Radvanyi, H
Junien, C
Coste, J
Laforet, P
Eymard, B
Becane, HM
Weber, S
Duboc, D
Citation: A. Lazarus et al., Sudden death in myotonic dystrophy: The potential role of bundle-branch reentry - Response, CIRCULATION, 101(5), 2000, pp. E73-E73
Authors:
Cherin, P
Authier, FJ
Gherardi, RK
Romero, N
Eymard, B
Herson, S
Caillat-Vigneron, N
Citation: P. Cherin et al., Gallium-67 scintigraphy in macrophagic myofasciitis, ARTH RHEUM, 43(7), 2000, pp. 1520-1526
Authors:
Richard, I
Bourg, N
Marchand, S
Alibert, O
Eymard, B
van der Kooi, AJ
Jackson, CE
Garcia, C
Burgunder, JM
Legum, C
de Visser, M
Fardeau, M
Beckmann, JS
Citation: I. Richard et al., A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies, NEUROMUSC D, 9(8), 1999, pp. 555-563
Authors:
Aissaoui, A
Klingel-Schmitt, I
Couderc, J
Chateau, D
Romagne, F
Jambou, F
Vincent, A
Levasseur, P
Eymard, B
Maillot, MC
Galanaud, P
Berrih-Aknin, S
Cohen-Kaminsky, S
Citation: A. Aissaoui et al., Prevention of autoimmune attack by targeting specific T-cell receptors in a severe combined immunodeficiency mouse model of myasthenia gravis, ANN NEUROL, 46(4), 1999, pp. 559-567
Authors:
Lazarus, A
Varin, J
Ounnoughene, Z
Radvanyi, H
Junien, C
Coste, J
Laforet, P
Eymard, B
Becane, HM
Weber, S
Duboc, D
Citation: A. Lazarus et al., Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy, CIRCULATION, 99(8), 1999, pp. 1041-1046
Authors:
Richard, I
Roudaut, C
Saenz, A
Pogue, R
Grimbergen, JEMA
Anderson, LVB
Beley, C
Cobo, AM
de Diego, C
Eymard, B
Gallano, P
Ginjaar, HB
Lasa, A
Pollitt, C
Topaloglu, H
Urtizberea, JA
de Visser, M
van der Kooi, A
Bushby, K
Bakker, E
de Munain, AL
Fardeau, M
Beckmann, JS
Citation: I. Richard et al., Calpainopathy - A survey of mutations and polymorphisms, AM J HU GEN, 64(6), 1999, pp. 1524-1540
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