-
1
-
-
0028215647
-
A new nomenclature for the laminins
-
Burgeson, R. E., M. Chiquet, R. Deutzmann, P. Ekblom, J. Engel, H. Kleinman, G. R. Martin, G Meneguzzi, M. Paulsson, J. Sanes et al: A new nomenclature for the laminins. Matrix Biol. 14 (1994) 209-211
-
(1994)
Matrix Biol.
, vol.14
, pp. 209-211
-
-
Burgeson, R.E.1
Chiquet, M.2
Deutzmann, R.3
Ekblom, P.4
Engel, J.5
Kleinman, H.6
Martin, G.R.7
Meneguzzi, G.8
Paulsson, M.9
Sanes, J.10
-
2
-
-
0022003048
-
Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles
-
David, T. J., R. M. Winter: Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles. J. Med. Genet. 22 (1985) 390-392
-
(1985)
J. Med. Genet.
, vol.22
, pp. 390-392
-
-
David, T.J.1
Winter, R.M.2
-
3
-
-
0027954337
-
Workshop report: 22nd ENMC sponsored workshop on congemtal muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993
-
Dubowitz, V.: Workshop report: 22nd ENMC sponsored workshop on congemtal muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993. Neuromusc Disord 4 (1994) 70-81
-
(1994)
Neuromusc Disord
, vol.4
, pp. 70-81
-
-
Dubowitz, V.1
-
4
-
-
0029060893
-
Workshop report: Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands
-
Dubowitz, V., M. Fardeau: Workshop report: proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands. Neuromusc. Disord. 5 (1995) 253-258
-
(1995)
Neuromusc. Disord.
, vol.5
, pp. 253-258
-
-
Dubowitz, V.1
Fardeau, M.2
-
6
-
-
0023694245
-
The prune belly syndrome: A review of its etiology, defects, treatment and prognosis
-
Greskovich, F. J., L. M. Nyberg: The prune belly syndrome: A review of its etiology, defects, treatment and prognosis. J. Urol. 140 (1988) 707-712
-
(1988)
J. Urol.
, vol.140
, pp. 707-712
-
-
Greskovich, F.J.1
Nyberg, L.M.2
-
7
-
-
0023203188
-
Familial absence of the trapezius muscle with associated shoulder girdle abnormalities
-
Gross-Kieselstein, E., R. S. Shalev: Familial absence of the trapezius muscle with associated shoulder girdle abnormalities. Clin. Genet 32 (1987) 145-147
-
(1987)
Clin. Genet
, vol.32
, pp. 145-147
-
-
Gross-Kieselstein, E.1
Shalev, R.S.2
-
8
-
-
0020626273
-
Part I. Amyoplasia: A common, sporadic condition with congenital contractures
-
Hall, J. G., S. D. Reed, E. P. Driscoll: Part I. Amyoplasia: A common, sporadic condition with congenital contractures. Am. J. Med. Genet. 15 (1983) 571-590
-
(1983)
Am. J. Med. Genet.
, vol.15
, pp. 571-590
-
-
Hall, J.G.1
Reed, S.D.2
Driscoll, E.P.3
-
9
-
-
0023098452
-
Obstructive lesions of the lower urinary tract in the prune belly syndrome
-
Hoagland, M. H., G. M. Hutchins: Obstructive lesions of the lower urinary tract in the prune belly syndrome. Arch. Pathol. Lab. Med 111 (1987) 154-156
-
(1987)
Arch. Pathol. Lab. Med
, vol.111
, pp. 154-156
-
-
Hoagland, M.H.1
Hutchins, G.M.2
-
10
-
-
0024375458
-
Congenital muscular dystrophy
-
Leyten, Q. H., F. J. M. Gabreës, W. O. Renier, H. J. ter Laak, R. C. A. Sengers, R. A. Mullaart: Congenital muscular dystrophy. J. Pediatr. 115 (1989) 214-221
-
(1989)
J. Pediatr.
, vol.115
, pp. 214-221
-
-
Leyten, Q.H.1
Gabreës, F.J.M.2
Renier, W.O.3
Ter Laak, H.J.4
Sengers, R.C.A.5
Mullaart, R.A.6
-
11
-
-
0027327154
-
Congenital muscular dystrophy: A study on the variability of morphological changes and dystrophin distribution in muscle biopsies
-
Leyten, Q. H., H. J. ter Laak, F. J. M. Gabreëls, W. O. Renier, R. C. A. Sengers: Congenital muscular dystrophy: A study on the variability of morphological changes and dystrophin distribution in muscle biopsies. Acta Neuropathol. 86 (1993) 386-392
-
(1993)
Acta Neuropathol.
, vol.86
, pp. 386-392
-
-
Leyten, Q.H.1
Ter Laak, H.J.2
Gabreëls, F.J.M.3
Renier, W.O.4
Sengers, R.C.A.5
-
12
-
-
0028903392
-
Somatosensory and visual evoked potentials in congenital muscular dystrophy: Correlation with MRI changes and muscle merosin status
-
Mercuri, E., F. Muntoni, A. Berardinelli, J. Pennock, C. Sewry, J. Philpot, V. Dubowitz: Somatosensory and visual evoked potentials in congenital muscular dystrophy: Correlation with MRI changes and muscle merosin status. Neuropediatrics 26 (1995) 3-7
-
(1995)
Neuropediatrics
, vol.26
, pp. 3-7
-
-
Mercuri, E.1
Muntoni, F.2
Berardinelli, A.3
Pennock, J.4
Sewry, C.5
Philpot, J.6
Dubowitz, V.7
-
13
-
-
0021269238
-
The pathogenesis of prune belly
-
Nakayama, D. K., M. R. Harrison, D. H. Chinn, A. A. De Lorimier: The pathogenesis of prune belly. Am. J Dis. Child. 138 (1984) 834-836
-
(1984)
Am. J Dis. Child.
, vol.138
, pp. 834-836
-
-
Nakayama, D.K.1
Harrison, M.R.2
Chinn, D.H.3
De Lorimier, A.A.4
-
14
-
-
0022544358
-
Association of amyoplasia with gastroschisis, bowel atresia and defects of the muscular layer of the trunk
-
Reid, C. O. M. V., J. G. Hall, C. Anderson, M. Bocian, J. Carey, T. Costa et al: Association of amyoplasia with gastroschisis, bowel atresia and defects of the muscular layer of the trunk. Am. J. Med. Genet. 24 (1986) 701-710
-
(1986)
Am. J. Med. Genet.
, vol.24
, pp. 701-710
-
-
Reid, C.O.M.V.1
Hall, J.G.2
Anderson, C.3
Bocian, M.4
Carey, J.5
Costa, T.6
-
15
-
-
0026022895
-
Prune belly syndrome in females: A triad of abdominal musculature deficiency and anomalies of the urinary and genital systems
-
Reinberg, Y., E. Shapiro, J. G. Manivel, C. B. Manley, G. Pettinato, R. Gonzalez: Prune belly syndrome in females: A triad of abdominal musculature deficiency and anomalies of the urinary and genital systems. J. Pediatr. 118 (1991) 395-398
-
(1991)
J. Pediatr.
, vol.118
, pp. 395-398
-
-
Reinberg, Y.1
Shapiro, E.2
Manivel, J.G.3
Manley, C.B.4
Pettinato, G.5
Gonzalez, R.6
-
16
-
-
0023661527
-
The prune belly syndrome: Experiences in nine patients
-
Smeitink, J., B. C. J. Hamel, R. von Empelen, J. D. M. de Vries, L. A. H. Monnens: The prune belly syndrome: Experiences in nine patients. Ned. Tijdschr. Geneeskd. 131 (1987) 489-492
-
(1987)
Ned. Tijdschr. Geneeskd.
, vol.131
, pp. 489-492
-
-
Smeitink, J.1
Hamel, B.C.J.2
Von Empelen, R.3
De Vries, J.D.M.4
Monnens, L.A.H.5
-
17
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Tomé, F. M. S., T. Evangelista, A. Leclerc, Y. Sunada, E. Manole, B. Estournet, A. Barois, K. P. Campbell, M. Fardeau: Congenital muscular dystrophy with merosin deficiency. C. R. Acad. Sci. Paris 317 (1994) 351-357
-
(1994)
C. R. Acad. Sci. Paris
, vol.317
, pp. 351-357
-
-
Tomé, 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
-
18
-
-
0029055267
-
2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy
-
2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy. Neuropediatrics 26 (1995) 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
Unsöld, R.8
Helliwell, T.R.9
Appleton, R.10
Lenard, H.G.11
|