-
1
-
-
85046525970
-
Myasthenia, thymoma, presynaptic antibodies, and a continuum of neuromuscular hyperexcitability
-
Ansevin CF. Myasthenia, thymoma, presynaptic antibodies, and a continuum of neuromuscular hyperexcitability. Neurology 2000;55:458.
-
(2000)
Neurology
, vol.55
, pp. 458
-
-
Ansevin, C.F.1
-
2
-
-
0033982579
-
Phenotypic variability in rippling muscle disease
-
Ansevin CF. Phenotypic variability in rippling muscle disease. Neurology 2000;54:273-274.
-
(2000)
Neurology
, vol.54
, pp. 273-274
-
-
Ansevin, C.F.1
-
3
-
-
0030063739
-
Rippling muscles and myasthenia gravis with rippling muscles
-
Ansevin CF, Agamanolis DP. Rippling muscles and myasthenia gravis with rippling muscles. Arch Neurol 1996;53:197-199.
-
(1996)
Arch Neurol
, vol.53
, pp. 197-199
-
-
Ansevin, C.F.1
Agamanolis, D.P.2
-
4
-
-
0034944010
-
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease
-
Betz RC, Schoser BG, Kasper D, Ricker K, Ramirez A, Stein V, Torbergsen T, Lee YA, Nothen MM, Wienker TF, Malin JP, Propping P, Reis A, Mortier W, Jentsch TJ, Vorgerd M, Kubisch C. Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease. Nat Genet 2001;28:218-219.
-
(2001)
Nat Genet
, vol.28
, pp. 218-219
-
-
Betz, R.C.1
Schoser, B.G.2
Kasper, D.3
Ricker, K.4
Ramirez, A.5
Stein, V.6
Torbergsen, T.7
Lee, Y.A.8
Nothen, M.M.9
Wienker, T.F.10
Malin, J.P.11
Propping, P.12
Reis, A.13
Mortier, W.14
Jentsch, T.J.15
Vorgerd, M.16
Kubisch, C.17
-
5
-
-
0034773570
-
Severe autosomal recessive rippling muscle disease
-
Koul RL, Chand RP, Chacko A, Ali M, Brown KM, Bushnarmuth SR, Escolar DM, Stephan DA. Severe autosomal recessive rippling muscle disease. Muscle Nerve 2001;24:1542-1547.
-
(2001)
Muscle Nerve
, vol.24
, pp. 1542-1547
-
-
Koul, R.L.1
Chand, R.P.2
Chacko, A.3
Ali, M.4
Brown, K.M.5
Bushnarmuth, S.R.6
Escolar, D.M.7
Stephan, D.A.8
-
6
-
-
0344255715
-
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease
-
Kubisch C, Schoser BG, von During M, Betz RC, Goebel HH, Zahn S, Ehrbrecht A, Aasly J, Schroers A, Popovic N, Lochmuller H, Schroder JM, Bruning T, Malin JP, Fricke B, Meinck HM, Torbergsen T, Engels H, Voss B, Vorgerd M. Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease. Ann Neurol 2003;53:512-520.
-
(2003)
Ann Neurol
, vol.53
, pp. 512-520
-
-
Kubisch, C.1
Schoser, B.G.2
Von During, M.3
Betz, R.C.4
Goebel, H.H.5
Zahn, S.6
Ehrbrecht, A.7
Aasly, J.8
Schroers, A.9
Popovic, N.10
Lochmuller, H.11
Schroder, J.M.12
Bruning, T.13
Malin, J.P.14
Fricke, B.15
Meinck, H.M.16
Torbergsen, T.17
Engels, H.18
Voss, B.19
Vorgerd, M.20
more..
-
7
-
-
0344286729
-
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis
-
Muller-Felber W, Ansevin CF, Ricker K, Muller-Jenssen A, Topfer M, Goebel HH, Pongratz DE. Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis. Neuromuscul Disord 1999;9:604-607.
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 604-607
-
-
Muller-Felber, W.1
Ansevin, C.F.2
Ricker, K.3
Muller-Jenssen, A.4
Topfer, M.5
Goebel, H.H.6
Pongratz, D.E.7
-
9
-
-
0035117623
-
Rippling muscle disease: Evidence for phenotypic and genetic heterogeneity
-
So YT, Zu L, Barraza C, Figueroa KP, Pulst SM. Rippling muscle disease: evidence for phenotypic and genetic heterogeneity. Muscle Nerve 2001;24:340-344.
-
(2001)
Muscle Nerve
, vol.24
, pp. 340-344
-
-
So, Y.T.1
Zu, L.2
Barraza, C.3
Figueroa, K.P.4
Pulst, S.M.5
-
10
-
-
0028116684
-
A rippling muscle disease gene is localized to 1q41: Evidence for multiple genes
-
Stephan DA, Buist NR, Chittenden AB, Ricker K, Zhou J, Hoffman EP. A rippling muscle disease gene is localized to 1q41: evidence for multiple genes. Neurology 1994;44:1915-1920.
-
(1994)
Neurology
, vol.44
, pp. 1915-1920
-
-
Stephan, D.A.1
Buist, N.R.2
Chittenden, A.B.3
Ricker, K.4
Zhou, J.5
Hoffman, E.P.6
-
11
-
-
0036123873
-
Rippling muscle syndrome preceding malignant lymphoma
-
Takagi A, Kojima S, Watanabe T, Ida M, Kawagoe S. Rippling muscle syndrome preceding malignant lymphoma. Intern Med 2002;41:147-150.
-
(2002)
Intern Med
, vol.41
, pp. 147-150
-
-
Takagi, A.1
Kojima, S.2
Watanabe, T.3
Ida, M.4
Kawagoe, S.5
-
12
-
-
0016693399
-
A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita Thomsen
-
Torbergsen T. A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita Thomsen. Acta Neurol Scand 1975;51:225-232.
-
(1975)
Acta Neurol Scand
, vol.51
, pp. 225-232
-
-
Torbergsen, T.1
-
13
-
-
0036259847
-
Rippling muscle disease: A review
-
Torbergsen T. Rippling muscle disease: a review. Muscle Nerve Suppl 2002;11:S103-S107.
-
(2002)
Muscle Nerve Suppl
, vol.11
-
-
Torbergsen, T.1
-
14
-
-
0032853220
-
Myasthenia, thymoma, presynaptic antibodies, and a continuum of neuromuscular hyperexcitability
-
Vernino S, Auger RG, Emslie-Smith AM, Harper CM, Lennon VA. Myasthenia, thymoma, presynaptic antibodies, and a continuum of neuromuscular hyperexcitability. Neurology 1999;53:1233-1239.
-
(1999)
Neurology
, vol.53
, pp. 1233-1239
-
-
Vernino, S.1
Auger, R.G.2
Emslie-Smith, A.M.3
Harper, C.M.4
Lennon, V.A.5
-
15
-
-
0036843065
-
Ion channel and striational antibodies define a continuum of autoimmune neuromuscular hyperexcitability
-
Vernino S, Lennon VA. Ion channel and striational antibodies define a continuum of autoimmune neuromuscular hyperexcitability. Muscle Nerve 2002;26:702-707.
-
(2002)
Muscle Nerve
, vol.26
, pp. 702-707
-
-
Vernino, S.1
Lennon, V.A.2
-
16
-
-
0033594454
-
Phenotypic variability in rippling muscle disease
-
Vorgerd M, Bolz H, Patzold T, Kubisch C, Malin JP, Mortier W. Phenotypic variability in rippling muscle disease. Neurology 1999;52:1453-1459.
-
(1999)
Neurology
, vol.52
, pp. 1453-1459
-
-
Vorgerd, M.1
Bolz, H.2
Patzold, T.3
Kubisch, C.4
Malin, J.P.5
Mortier, W.6
-
17
-
-
0035956556
-
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation
-
Vorgerd M, Ricker K, Ziemssen F, Kress W, Goebel HH, Nix WA, Kubisch C, Schoser BG, Mortier W. A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation. Neurology 2001;57:2273-2277.
-
(2001)
Neurology
, vol.57
, pp. 2273-2277
-
-
Vorgerd, M.1
Ricker, K.2
Ziemssen, F.3
Kress, W.4
Goebel, H.H.5
Nix, W.A.6
Kubisch, C.7
Schoser, B.G.8
Mortier, W.9
|