-
1
-
-
0030879625
-
Changes of lamininβ-2 chain expression in congenital muscular dystrophy
-
Cohn RD, Hermann R, Wewer UM, Voit T (1997) Changes of lamininβ-2 chain expression in congenital muscular dystrophy. Neuromusc Disord 7: 373-378
-
(1997)
Neuromusc Disord
, vol.7
, pp. 373-378
-
-
Cohn, R.D.1
Hermann, R.2
Wewer, U.M.3
Voit, T.4
-
2
-
-
0029000061
-
Lissencephaly and other malformations of cortical development: 1995 update
-
Dobyns WB, Truwit CL (1995) Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics 26: 132-147
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
3
-
-
0024539092
-
Diagnostic criteria for Walker Warburg syndrome
-
Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Rohinow M (1989) Diagnostic criteria for Walker Warburg syndrome. Am J Med Genet 32: 195-210
-
(1989)
Am J Med Genet
, vol.32
, pp. 195-210
-
-
Dobyns, W.B.1
Pagon, R.A.2
Armstrong, D.3
Curry, C.J.4
Greenberg, F.5
Grix, A.6
Holmes, L.B.7
Laxova, R.8
Michels, V.V.9
Rohinow, M.10
-
5
-
-
0347733184
-
Peripheral and central nervous system involvement in merosin-deficient congenital muscular dystrophy
-
Dubowitz V, Mercuri E, Muntoni F, Philpot J, Sewry CA, Shorer Z (1995) Peripheral and central nervous system involvement in merosin-deficient congenital muscular dystrophy. Neurology 45 [Suppl 4]: A407
-
(1995)
Neurology
, vol.45
, Issue.4 SUPPL.
-
-
Dubowitz, V.1
Mercuri, E.2
Muntoni, F.3
Philpot, J.4
Sewry, C.A.5
Shorer, Z.6
-
6
-
-
0030951457
-
Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse
-
Matsumura K, Yamada H, Saito F, Sunada Y, Shimuzu T (1997) Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Neuromusc Disord 7: 7-12
-
(1997)
Neuromusc Disord
, vol.7
, pp. 7-12
-
-
Matsumura, K.1
Yamada, H.2
Saito, F.3
Sunada, Y.4
Shimuzu, T.5
-
7
-
-
0029012558
-
Muscle-eye-brain diesease and Fukuyama-type congenital muscular dystrophy are not allelic
-
Ranta S, Pihko H, Santavuori P, Tahvanainen E, Chapelle A de la (1995) Muscle-eye-brain diesease and Fukuyama-type congenital muscular dystrophy are not allelic. Neuromusc Disord 5: 283-286
-
(1995)
Neuromusc Disord
, vol.5
, pp. 283-286
-
-
Ranta, S.1
Pihko, H.2
Santavuori, P.3
Tahvanainen, E.4
De La Chapelle, A.5
-
8
-
-
0027957756
-
Meningeal cells organise the superficial glia limitans of the cerebellum and produce components of both the interstitial matrix and the basement membrane
-
Sievers J, Phelemann FW, Gude S, Berry M (1994) Meningeal cells organise the superficial glia limitans of the cerebellum and produce components of both the interstitial matrix and the basement membrane. J Neurocytol 23: 135-149
-
(1994)
J Neurocytol
, vol.23
, pp. 135-149
-
-
Sievers, J.1
Phelemann, F.W.2
Gude, S.3
Berry, M.4
-
9
-
-
0030612270
-
Presence of laminin α5 chain and lack of laminin α1 chain during human muscle development and in muscular dystrophies
-
Tiger CF, Champliaud MF, Pedrosa Domello F, Thornell L, Ekblom P, Gullberg D (1997) Presence of laminin α5 chain and lack of laminin α1 chain during human muscle development and in muscular dystrophies. J Biol Chem 272: 28590-28595
-
(1997)
J Biol Chem
, vol.272
, pp. 28590-28595
-
-
Tiger, C.F.1
Champliaud, M.F.2
Pedrosa Domello, F.3
Thornell, L.4
Ekblom, P.5
Gullberg, D.6
-
10
-
-
0028931768
-
Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome
-
Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y (1995) Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome. Ann Neurol 37: 99-101
-
(1995)
Ann Neurol
, vol.37
, pp. 99-101
-
-
Toda, T.1
Yoshioka, M.2
Nakahori, Y.3
Kanazawa, I.4
Nakamura, Y.5
Nakagome, Y.6
-
11
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Paris
-
Tomè FMS, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M (1994) Congenital muscular dystrophy with merosin deficiency. C R Acad Sci (Paris) 317: 351-357
-
(1994)
C R Acad Sci
, vol.317
, pp. 351-357
-
-
Tomè, F.M.S.1
Evangelista, T.2
Leclerc, A.3
Sunada, Y.4
Manole, E.5
Estournet, B.6
Barois, A.7
Campbell, K.P.8
Fardeau, M.9
-
12
-
-
0030898515
-
Localization of laminin α2 in the human retina. Possible significance for congenital muscular dystrophy associated with laminin α2 deficiency
-
Toti P, De Felice C, Malandrini A, Megha T, Cardone C, Villanova M (1997) Localization of laminin α2 in the human retina. Possible significance for congenital muscular dystrophy associated with laminin α2 deficiency. Neuromusc Disord 7: 21-26
-
(1997)
Neuromusc Disord
, vol.7
, pp. 21-26
-
-
Toti, P.1
De Felice, C.2
Malandrini, A.3
Megha, T.4
Cardone, C.5
Villanova, M.6
-
13
-
-
0030825922
-
Localization of laminin α2 chain in normal central nervous system: An immunofluorescence and ultrastructural study
-
Villanova M, Sewry CA, Malandrini A, Sabatelli P, Toti P, Squarzoni S, Torelli S, Six J, Scarfo G, Palma L, Muntoni F, Maraldi NM, Guazzi GC (1997) Localization of laminin α2 chain in normal central nervous system: an immunofluorescence and ultrastructural study. Acta Neuropathol 94: 567-571
-
(1997)
Acta Neuropathol
, vol.94
, pp. 567-571
-
-
Villanova, M.1
Sewry, C.A.2
Malandrini, A.3
Sabatelli, P.4
Toti, P.5
Squarzoni, S.6
Torelli, S.7
Six, J.8
Scarfo, G.9
Palma, L.10
Muntoni, F.11
Maraldi, N.M.12
Guazzi, G.C.13
-
14
-
-
0029055267
-
Preserved merosin M-chain (or laminin α2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin deficient congenital muscular dystrophy
-
Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Linsold R, Helliwel TR, Appleton R, Lenard HG (1995) Preserved merosin M-chain (or laminin α2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin deficient congenital muscular dystrophy. Neuropediatrics 26: 148-155
-
(1995)
Neuropediatrics
, vol.26
, pp. 148-155
-
-
Voit, T.1
Sewry, C.A.2
Meyer, K.3
Hermann, R.4
Straub, V.5
Muntoni, F.6
Kahn, T.7
Linsold, R.8
Helliwel, T.R.9
Appleton, R.10
Lenard, H.G.11
-
15
-
-
0029396750
-
Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy)
-
Wewer UM, Durkin ME, Zhang X, Laursen H, Nielsen NH, Towfighi J, Engvall E, Albrechtensen A (1995) Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy). Neurology 45: 2099-2101
-
(1995)
Neurology
, vol.45
, pp. 2099-2101
-
-
Wewer, U.M.1
Durkin, M.E.2
Zhang, X.3
Laursen, H.4
Nielsen, N.H.5
Towfighi, J.6
Engvall, E.7
Albrechtensen, A.8
-
16
-
-
0030610326
-
Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle
-
Wewer UM, Thornell LE, Loechel F, Zhang X, Durkin ME, Amano S, Burgeson RE, Engvall E, Albrechtsen R, Virtanen I (1997) Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle. Am J Pathol 151: 621-631
-
(1997)
Am J Pathol
, vol.151
, pp. 621-631
-
-
Wewer, U.M.1
Thornell, L.E.2
Loechel, F.3
Zhang, X.4
Durkin, M.E.5
Amano, S.6
Burgeson, R.E.7
Engvall, E.8
Albrechtsen, R.9
Virtanen, I.10
|