-
1
-
-
0027954337
-
22nd ENMC sponsored workshop on congenital muscular dystrophy Baarn the Netherlands
-
Dubowitz V. 22nd ENMC sponsored workshop on congenital muscular dystrophy Baarn The Netherlands. Neuromusc Disord 1994;4:75-81.
-
(1994)
Neuromusc Disord
, vol.4
, pp. 75-81
-
-
Dubowitz, V.1
-
2
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Tome FMS, Evangelista T, Leclerc A, et al. Congenital muscular dystrophy with merosin deficiency. CR Acad Sci Paris, Life Sci 1994;317:351-357.
-
(1994)
CR Acad Sci Paris, Life Sci
, vol.317
, pp. 351-357
-
-
Tome, F.M.S.1
Evangelista, T.2
Leclerc, A.3
-
3
-
-
0030220589
-
41st ENMC International workshop on congenital muscular dystrophy
-
Dubowitz V. 41st ENMC International workshop on congenital muscular dystrophy. Neuromusc Disord 1996;6:295-306.
-
(1996)
Neuromusc Disord
, vol.6
, pp. 295-306
-
-
Dubowitz, V.1
-
4
-
-
0028094441
-
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
-
Hillaire D, Leclerc A, Faure S, et al. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Hum Mol Genet 1994;3:1657-1661.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1657-1661
-
-
Hillaire, D.1
Leclerc, A.2
Faure, S.3
-
5
-
-
17344373746
-
PCR based mutation screening of the laminin alpha 2 chain gene (LAMA2): Application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy
-
Guicheney P, Vignier N, Zhang X, et al. PCR based mutation screening of the laminin alpha 2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. J Med Genet. 1998;35:211-217.
-
(1998)
J Med Genet.
, vol.35
, pp. 211-217
-
-
Guicheney, P.1
Vignier, N.2
Zhang, X.3
-
6
-
-
0022502986
-
Congenital muscular dystrophy and cerebral CT scan anomalies Results of a collaborative study of the Societe de Neurologie Infantile
-
Echenne B, Arthuis M, Billard C, et al. Congenital muscular dystrophy and cerebral CT scan anomalies Results of a collaborative study of the Societe de Neurologie Infantile. J Neurol Sci 1986;75:7-22.
-
(1986)
J Neurol Sci
, vol.75
, pp. 7-22
-
-
Echenne, B.1
Arthuis, M.2
Billard, C.3
-
7
-
-
0029061267
-
Clinical phenotype in congenital muscular dystrophy: Correlation with expression of merosin in skeletal muscle
-
Philpot J, Sewry C, Pennock J, Dubowitz V. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle. Neuromusc Disord 1995;5:301-305.
-
(1995)
Neuromusc Disord
, vol.5
, pp. 301-305
-
-
Philpot, J.1
Sewry, C.2
Pennock, J.3
Dubowitz, V.4
-
8
-
-
8044233952
-
Sequential study of central and peripheral nervous system involvement in an infant with merosindeficient congenital muscular dystrophy
-
Mercuri E, Pennock J, Goodwin F, et al. Sequential study of central and peripheral nervous system involvement in an infant with merosindeficient congenital muscular dystrophy. Neuromusc Disord. 1996;6:425-429.
-
(1996)
Neuromusc Disord.
, vol.6
, pp. 425-429
-
-
Mercuri, E.1
Pennock, J.2
Goodwin, F.3
-
9
-
-
0011289177
-
Congenital muscular dystrophy
-
van der Knaap MS, Valk J. Congenital muscular dystrophy. In: Magnetic resonance of myelin, myelinatton, and myelin disorders, 2nd 1995:267-276.
-
(1995)
Magnetic Resonance of Myelin, Myelinatton, and Myelin Disorders, 2nd
, pp. 267-276
-
-
Van Der Knaap, M.S.1
Valk, J.2
-
10
-
-
85008070304
-
Laminin in animal models for muscular dystrophy: Defect of laminin M in skeletal and cardiac muscles and peripheral nerve of homozygous dystrophic dy/dy mice
-
Arahata K, Hayashi YK, Koga R, et al. Laminin in animal models for muscular dystrophy: defect of laminin M in skeletal and cardiac muscles and peripheral nerve of homozygous dystrophic dy/dy mice. Proc Jpn Acad. 1993;69:259-264.
-
(1993)
Proc Jpn Acad.
, vol.69
, pp. 259-264
-
-
Arahata, K.1
Hayashi, Y.K.2
Koga, R.3
-
11
-
-
0028318185
-
Deficiency of merosin in dystrophic dy mice and genetic-linkage of laminin m-chain gene to dy locus
-
Sunada Y, Bernier SM, Kozak CA, Yamada Y, Campbell KP. Deficiency of merosin in dystrophic dy mice and genetic-linkage of laminin m-chain gene to dy locus. J Biol Chem. 1994;269:13729-13732.
-
(1994)
J Biol Chem.
, vol.269
, pp. 13729-13732
-
-
Sunada, Y.1
Bernier, S.M.2
Kozak, C.A.3
Yamada, Y.4
Campbell, K.P.5
-
12
-
-
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; 10:472-475.
-
(1995)
J Child Neurol
, vol.10
, pp. 472-475
-
-
Shorer, Z.1
Philpot, J.2
Muntoni, F.3
-
13
-
-
0016688925
-
Neural abnormalities in the dystrophic mouse
-
Bradley WG, Jenkison M. Neural abnormalities in the dystrophic mouse. J Neurol Sci 1975;25:249-255.
-
(1975)
J Neurol Sci
, vol.25
, pp. 249-255
-
-
Bradley, W.G.1
Jenkison, M.2
-
14
-
-
0030951457
-
Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse
-
Review
-
Matsumura C, Yamada H, Saito F, et al. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Neuromusc Disord 1997;7:7-12 (Review).
-
(1997)
Neuromusc Disord
, vol.7
, pp. 7-12
-
-
Matsumura, C.1
Yamada, H.2
Saito, F.3
-
15
-
-
0000186844
-
Dystrophia muscularis: A hereditary primary myopathy in the house mouse
-
Michelson AM, Russell ES, Harman PJ. Dystrophia muscularis: a hereditary primary myopathy in the house mouse. Proc Natl Acad Sci USA 1955;41:1079-1084.
-
(1955)
Proc Natl Acad Sci USA
, vol.41
, pp. 1079-1084
-
-
Michelson, A.M.1
Russell, E.S.2
Harman, P.J.3
-
16
-
-
0031909144
-
High-resolution in vivo measurements of transverse relaxation times in rats at 7 Tesla
-
Cremillieux Y, Ding S, Dunn JF. High-resolution in vivo measurements of transverse relaxation times in rats at 7 Tesla. Magn Reson Med 1998;39:285-290.
-
(1998)
Magn Reson Med
, vol.39
, pp. 285-290
-
-
Cremillieux, Y.1
Ding, S.2
Dunn, J.F.3
-
17
-
-
0026648372
-
In vivo relaxation times and hydrogen density at 0.063-4.85 T in rats with implanted mammary adenocarcinomas
-
Chen JH, Avram HE, Crooks LE, Arakawa M, Kaufman L, Brito AC. In vivo relaxation times and hydrogen density at 0.063-4.85 T in rats with implanted mammary adenocarcinomas. Radiology 1992;184:427-434.
-
(1992)
Radiology
, vol.184
, pp. 427-434
-
-
Chen, J.H.1
Avram, H.E.2
Crooks, L.E.3
Arakawa, M.4
Kaufman, L.5
Brito, A.C.6
-
18
-
-
0028803360
-
Changes of relaxation times (Tl T2) and apparent diffusion coefficient after permanent middle cerebral artery occlusion in the rat: Temporal evolution regional extent, and comparison with histology
-
Hoehn-Berlage M, Eis M, Back T, Kohno K, Yamashita K. Changes of relaxation times (Tl T2) and apparent diffusion coefficient after permanent middle cerebral artery occlusion in the rat: temporal evolution regional extent, and comparison with histology. Magn Reson Med 1995;34:824-834.
-
(1995)
Magn Reson Med
, vol.34
, pp. 824-834
-
-
Hoehn-Berlage, M.1
Eis, M.2
Back, T.3
Kohno, K.4
Yamashita, K.5
-
19
-
-
0022872540
-
Rare Imaging - A fast imaging method for clinical MR
-
Hennig J, Nauerth A, Friedburg H. Rare Imaging - A fast imaging method for clinical MR. Mag Reson Med 1986(3):823-833.
-
(1986)
Mag Reson Med
, Issue.3
, pp. 823-833
-
-
Hennig, J.1
Nauerth, A.2
Friedburg, H.3
-
20
-
-
0024415461
-
The synthesis of soft pulses with a specified frequency response
-
Shinnar M, Bolinger L, Leigh JS. The synthesis of soft pulses with a specified frequency response. Magn Reson Med 1989; 12:88-92.
-
(1989)
Magn Reson Med
, vol.12
, pp. 88-92
-
-
Shinnar, M.1
Bolinger, L.2
Leigh, J.S.3
-
21
-
-
0026116321
-
Parameter relations for the Shinnar-Le Roux selective excitation pulse design algorithm
-
Pauly J, Le Roux P, Nishimura D, Macovski A. Parameter relations for the Shinnar-Le Roux selective excitation pulse design algorithm. IEEE Trans Med Imag 1991; 10:53-65.
-
(1991)
IEEE Trans Med Imag
, vol.10
, pp. 53-65
-
-
Pauly, J.1
Le Roux, P.2
Nishimura, D.3
Macovski, A.4
-
22
-
-
0031950648
-
Differential labelling of laminin α2 in muscle and neural tissue of dy/dy mice; are there isoforms of the laminin α2 chain?
-
erratum p. 166.
-
Sewry CA, Uziyel Y, Torelli S, et al. Differential labelling of laminin α2 in muscle and neural tissue of dy/dy mice; are there isoforms of the laminin α2 chain? Neuropath Appl Neurobiol 1998;24:66-72 (erratum p. 166).
-
(1998)
Neuropath Appl Neurobiol
, vol.24
, pp. 66-72
-
-
Sewry, C.A.1
Uziyel, Y.2
Torelli, S.3
-
23
-
-
0030990635
-
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency
-
Tan F, Topaloglu H, Sewry C, et al. Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromusc Disord 1997;7:85-89.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 85-89
-
-
Tan, F.1
Topaloglu, H.2
Sewry, C.3
-
24
-
-
0032867544
-
68th ENMC International Workshop (5th International Workshop) on congenital muscular dystrophy, Naarden, the Netherlands
-
Dubowitz V. 68th ENMC International Workshop (5th International Workshop) on congenital muscular dystrophy, Naarden, The Netherlands. Neuromusc Disord 1999;9:446-454.
-
(1999)
Neuromusc Disord
, vol.9
, pp. 446-454
-
-
Dubowitz, V.1
-
26
-
-
0027971891
-
Imaging neuronal development with magnetic resonance imaging (NMR) microscopy
-
Jacobs RE, Fraser SE. Imaging neuronal development with magnetic resonance imaging (NMR) microscopy. J Neurosci Methods 1994;54:189-196.
-
(1994)
J Neurosci Methods
, vol.54
, pp. 189-196
-
-
Jacobs, R.E.1
Fraser, S.E.2
-
28
-
-
0030879625
-
Changes of laminin beta 2 chain expression in congenital muscular dystrophy
-
Cohn RD, Herrmann R, Wewer UM, Voit T. Changes of laminin beta 2 chain expression in congenital muscular dystrophy. Neuromusc Disord 1997;7:373-378.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 373-378
-
-
Cohn, R.D.1
Herrmann, R.2
Wewer, U.M.3
Voit, T.4
-
29
-
-
0033540112
-
Expression of laminin α1, α2, α4, and α5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice
-
Ringelmann B, Roder C, Hallmann R, et al. Expression of laminin α1, α2, α4, and α5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice. Exp Cell Res 1999;246:165-182.
-
(1999)
Exp Cell Res
, vol.246
, pp. 165-182
-
-
Ringelmann, B.1
Roder, C.2
Hallmann, R.3
-
30
-
-
0030769794
-
Laminins of the adult mammalian CNS; laminin-alpha2 (merosin M-) chain immunoreactivity is associated with neuronal processes
-
Hagg T, Portera-Cailliau C, Jucker M, Engvall E. Laminins of the adult mammalian CNS; laminin-alpha2 (merosin M-) chain immunoreactivity is associated with neuronal processes. Brain Res 1997;764:17-27.
-
(1997)
Brain Res
, vol.764
, pp. 17-27
-
-
Hagg, T.1
Portera-Cailliau, C.2
Jucker, M.3
Engvall, E.4
-
31
-
-
0031181374
-
Localisation of several laminin chains in the normal human central and peripheral nervous system
-
Villanova M, Sewry CA, Malandrini A, et al. Localisation of several laminin chains in the normal human central and peripheral nervous system. J Submicrosc Cytol Pathol 1997;29:409-413.
-
(1997)
J Submicrosc Cytol Pathol
, vol.29
, pp. 409-413
-
-
Villanova, M.1
Sewry, C.A.2
Malandrini, A.3
-
32
-
-
0030825922
-
Localization of laminin alpha 2 chain in normal human central nervous system: An immunofluorescence and ultrastructural study
-
Villanova M, Malandrini A, Sabatelli P, et al. Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study. Acta Neuropathol 1997;94:567-571.
-
(1997)
Acta Neuropathol
, vol.94
, pp. 567-571
-
-
Villanova, M.1
Malandrini, A.2
Sabatelli, P.3
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