-
1
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Tome FMS, Evangelista T, Ledere A, et al. Congenital muscular dystrophy with merosin deficiency. C R Acad Sci, Paris, Life Sc 1994;317:351-7.
-
(1994)
C R Acad Sci, Paris, Life Sc
, vol.317
, pp. 351-357
-
-
Tome, F.M.S.1
Evangelista, T.2
Ledere, A.3
-
2
-
-
0002478883
-
Congenital muscular dystrophies in muscular disorders
-
In: Emery EHA, editor; Chichester: John Wiley & Sons
-
Tome FMS, Guicheney P, Fardeau M. Congenital muscular dystrophies in muscular disorders. In: Emery EHA, editor. Clinical and Molecular Genetics. Chichester: John Wiley & Sons; 1998. pp. 21-57.
-
(1998)
Clinical and Molecular Genetics.
, pp. 21-57
-
-
Tome, F.M.S.1
Guicheney, P.2
Fardeau, M.3
-
3
-
-
0001717036
-
Case of myositis fibroma with pathological examination
-
Batten FE. Case of myositis fibroma with pathological examination. Brain 1903;26:147-8.
-
(1903)
Brain
, vol.26
, pp. 147-148
-
-
Batten, F.E.1
-
4
-
-
0000827668
-
A case of congenital defect of the muscular system (dystrophia musculairs congenital) and its association with congenital talipes equino-varus
-
Howard R. A case of congenital defect of the muscular system (dystrophia musculairs congenital) and its association with congenital talipes equino-varus. Proc R Soc Med 1908;1:157-66.
-
(1908)
Proc R Soc Med
, vol.1
, pp. 157-166
-
-
Howard, R.1
-
5
-
-
0028094441
-
Localization of merosin negative congenital muscular dystrophy to chromosome 6q 2 by homozygosity mapping
-
Hillaire D, Leclerc A, Faure S, et al. Localization of merosin negative congenital muscular dystrophy to chromosome 6q 2 by homozygosity mapping. Hum Med Genet 1994;3:1657-61.
-
(1994)
Hum Med Genet
, vol.3
, pp. 1657-1661
-
-
Hillaire, D.1
Leclerc, A.2
Faure, S.3
-
6
-
-
0029794008
-
Merosin and laminin in myogenesis; Specific requirement for merosin in myotube stability and survival
-
Vachon PH, Loechel F, Xu H, et al. Merosin and laminin in myogenesis; Specific requirement for merosin in myotube stability and survival. J Cell Biol 1996;134:1483-97.
-
(1996)
J Cell Biol
, vol.134
, pp. 1483-1497
-
-
Vachon, P.H.1
Loechel, F.2
Xu, H.3
-
7
-
-
0030918601
-
Variable clinical phenotype in merosin deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain
-
Sewry CA, Naom I, D'Alessandro M, et al. Variable clinical phenotype in merosin deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain. Neuromusc Disord 1997;7:169-75.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 169-175
-
-
Sewry, C.A.1
Naom, I.2
D'Alessandro, M.3
-
8
-
-
0028788685
-
Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy
-
Shorer Z, Philpot J, Muntoni F, et al. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy. J Child Neurol 1995;10:472-5.
-
(1995)
J Child Neurol
, vol.10
, pp. 472-475
-
-
Shorer, Z.1
Philpot, J.2
Muntoni, F.3
-
9
-
-
0030997888
-
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: From identification of mutations to prenatal diagnosis
-
Guicheney P, Vignier N, Helbling-Leclerc A, et al. Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: From identification of mutations to prenatal diagnosis. Neuromusc Disord 1997;7:180-6.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 180-186
-
-
Guicheney, P.1
Vignier, N.2
Helbling-Leclerc, A.3
-
10
-
-
0028318185
-
Deficiency of merosin in dystrophic dy mice and genetic linkage of the laminin M chain gene to dy locus
-
Sunada Y, Bernier SM, Kozak CA, et al. Deficiency of merosin in dystrophic dy mice and genetic linkage of the laminin M chain gene to dy locus. J Biol Chem 1994;269:13729-32.
-
(1994)
J Biol Chem
, vol.269
, pp. 13729-13732
-
-
Sunada, Y.1
Bernier, S.M.2
Kozak, C.A.3
-
11
-
-
0028135436
-
Murine muscular dystrophy caused by mutation in laminin alpha 2 (LAMA 2) gene
-
Xu H, Wu XR, Wewer VM, et al. Murine muscular dystrophy caused by mutation in laminin alpha 2 (LAMA 2) gene. Nat Genet 1994;8:297-302.
-
(1994)
Nat Genet
, vol.8
, pp. 297-302
-
-
Xu, H.1
Wu, X.R.2
Wewer, V.M.3
|