-
2
-
-
0023122493
-
Disorders of neuronal migration
-
Barth PG. 1987. Disorders of neuronal migration. Can J Neurol Sci 14: 1-16.
-
(1987)
Can J Neurol Sci
, vol.14
, pp. 1-16
-
-
Barth, P.G.1
-
3
-
-
0021212099
-
Interhemispheral neuro-epithelial (glio-ependymal) cysts, associated with agenesis of the corpus callosum and neocortical maldevelopment. A case study
-
Barth PG, Uylings HB, Stam FC. 1984. Interhemispheral neuro-epithelial (glio-ependymal) cysts, associated with agenesis of the corpus callosum and neocortical maldevelopment. A case study. Child's Brain 11: 312-319.
-
(1984)
Child's Brain
, vol.11
, pp. 312-319
-
-
Barth, P.G.1
Uylings, H.B.2
Stam, F.C.3
-
4
-
-
0026052812
-
Choroid plexus dysmorphism detected by transvaginal sonography: The earliest sign of fetal hydrocephalus
-
Bronshtein M, Ben-Shlomo I. 1991. Choroid plexus dysmorphism detected by transvaginal sonography: the earliest sign of fetal hydrocephalus. J Clin Ultrasound 19: 547-553.
-
(1991)
J Clin Ultrasound
, vol.19
, pp. 547-553
-
-
Bronshtein, M.1
Ben-Shlomo, I.2
-
5
-
-
9044220611
-
Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas
-
Carbonara C, Longa L, Grosso E, Mazzucco G, Borrone C, Garre ML, Brisigotti M, Filippi G, Scabar A, Giannotti A, Falzoni P, Monga G, Garini G, Gabrielli M, Riegler P, Danesino C, Ruggieri M, Magro G, Migone N. 1996. Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas. Genes Chromosomes Cancer 15: 18-25.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 18-25
-
-
Carbonara, C.1
Longa, L.2
Grosso, E.3
Mazzucco, G.4
Borrone, C.5
Garre, M.L.6
Brisigotti, M.7
Filippi, G.8
Scabar, A.9
Giannotti, A.10
Falzoni, P.11
Monga, G.12
Garini, G.13
Gabrielli, M.14
Riegler, P.15
Danesino, C.16
Ruggieri, M.17
Magro, G.18
Migone, N.19
-
6
-
-
0023788351
-
Role of prenatal detection of cardiac tumours in the diagnosis of tuberous sclerosis-report of two cases
-
Chitayat D, McGillivray BC, Diamant S, Wittmann BK, Sandor GGS. 1988. Role of prenatal detection of cardiac tumours in the diagnosis of tuberous sclerosis-report of two cases. Prenat Diagn 8: 577-584.
-
(1988)
Prenat Diagn
, vol.8
, pp. 577-584
-
-
Chitayat, D.1
McGillivray, B.C.2
Diamant, S.3
Wittmann, B.K.4
Sandor, G.G.S.5
-
7
-
-
0027770784
-
Identification and characterization of the tuberous sclerosis gene on chromosome 16
-
European Chromosome 16 Tuberous Sclerosis Consortium 1993. Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 75: 1305-1315.
-
(1993)
Cell
, vol.75
, pp. 1305-1315
-
-
-
8
-
-
0018891706
-
Tuberous sclerosis: The incidence of sporadic cases versus familial cases
-
Fleury P, de Groot WP, Delleman JW, Verbeeten B, Frankenmolen-Witkiezwicz IM. 1980. Tuberous sclerosis: the incidence of sporadic cases versus familial cases. Brain Dev 2: 107-117.
-
(1980)
Brain Dev
, vol.2
, pp. 107-117
-
-
Fleury, P.1
De Groot, W.P.2
Delleman, J.W.3
Verbeeten, B.4
Frankenmolen-Witkiezwicz, I.M.5
-
10
-
-
0025147135
-
Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma
-
Harding CO, Pagon RA. 1990. Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma. Am J Med Genet 37: 443-446.
-
(1990)
Am J Med Genet
, vol.37
, pp. 443-446
-
-
Harding, C.O.1
Pagon, R.A.2
-
11
-
-
0029840253
-
Glioependymal and arachnoid cysts: Unusual causes of early ventriculomegaly in utero
-
Hassan J, Sepulveda W, Teixeira J, Cox PM. 1996. Glioependymal and arachnoid cysts: unusual causes of early ventriculomegaly in utero. Prenat Diagn 16: 729-733.
-
(1996)
Prenat Diagn
, vol.16
, pp. 729-733
-
-
Hassan, J.1
Sepulveda, W.2
Teixeira, J.3
Cox, P.M.4
-
12
-
-
0029831886
-
Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions
-
Henske EP, Scheithauer BW, Short PM, Wollmann R, Nahmias J, Hornigold N, van Slegtenhorst M, Welsh CT, Kwiatkowski DJ. 1996. Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions. Hum Genet 59: 400-406.
-
(1996)
Hum Genet
, vol.59
, pp. 400-406
-
-
Henske, E.P.1
Scheithauer, B.W.2
Short, P.M.3
Wollmann, R.4
Nahmias, J.5
Hornigold, N.6
Van Slegtenhorst, M.7
Welsh, C.T.8
Kwiatkowski, D.J.9
-
13
-
-
0022542111
-
Prenatal diagnosis of familial tuberous sclerosis following detection of cardiac rhabdomyoma by ultrasound
-
Journel H, Roussey M, Plais MH, Milon J, Almange C, Le Marec B. 1986. Prenatal diagnosis of familial tuberous sclerosis following detection of cardiac rhabdomyoma by ultrasound. Prenat Diagn 6: 283-289.
-
(1986)
Prenat Diagn
, vol.6
, pp. 283-289
-
-
Journel, H.1
Roussey, M.2
Plais, M.H.3
Milon, J.4
Almange, C.5
Le Marec, B.6
-
15
-
-
0026467746
-
Magnetic resonance imaging in antenatal diagnosis of tuberous sclerosis
-
Mirlesse V, Wener H, Jacquemard F, Perotez C, Daffos F, Sonigo P, Brunelle F. 1992. Magnetic resonance imaging in antenatal diagnosis of tuberous sclerosis. Lancet 340: 1163.
-
(1992)
Lancet
, vol.340
, pp. 1163
-
-
Mirlesse, V.1
Wener, H.2
Jacquemard, F.3
Perotez, C.4
Daffos, F.5
Sonigo, P.6
Brunelle, F.7
-
16
-
-
0023046006
-
Antenatal ultrasonographic findings in tuberous sclerosis. Report of 2 cases
-
Muller L, De Jong G, Falck V, Hewlett R, Hunter J, Shires J. 1986. Antenatal ultrasonographic findings in tuberous sclerosis. Report of 2 cases. S Afr Med J 69: 633-638.
-
(1986)
S Afr Med J
, vol.69
, pp. 633-638
-
-
Muller, L.1
De Jong, G.2
Falck, V.3
Hewlett, R.4
Hunter, J.5
Shires, J.6
-
17
-
-
0028168936
-
Two loci for tuberous sclerosis: One on 9q34 and one on 16p13
-
Povey S, Burley MW, Attwood J, Benham F, Hunt D, Jeremiah SJ, Franklin D, Gillett G, Malas S, Robson EB, Tippett P, Edwards JH, Kwiatkowski DJ, Super M, Mueller R, Fryer A, Clarke A, Webb D, Osborne J. 1994. Two loci for tuberous sclerosis: one on 9q34 and one on 16p13. Ann Hum Genet 58: 107-127.
-
(1994)
Ann Hum Genet
, vol.58
, pp. 107-127
-
-
Povey, S.1
Burley, M.W.2
Attwood, J.3
Benham, F.4
Hunt, D.5
Jeremiah, S.J.6
Franklin, D.7
Gillett, G.8
Malas, S.9
Robson, E.B.10
Tippett, P.11
Edwards, J.H.12
Kwiatkowski, D.J.13
Super, M.14
Mueller, R.15
Fryer, A.16
Clarke, A.17
Webb, D.18
Osborne, J.19
-
18
-
-
0027484920
-
Magnetic resonance imaging of the fetus: A study of 20 cases performed without curarization
-
Revel MP, Pons JC, Fournet P, Vial M, Musset D, Labrune M, Frydman R. 1993. Magnetic resonance imaging of the fetus: a study of 20 cases performed without curarization. Prenat Diagn 13: 775-799.
-
(1993)
Prenat Diagn
, vol.13
, pp. 775-799
-
-
Revel, M.P.1
Pons, J.C.2
Fournet, P.3
Vial, M.4
Musset, D.5
Labrune, M.6
Frydman, R.7
-
19
-
-
0030068465
-
Prenatal MRI diagnosis of fetal cerebral tuberous sclerosis
-
Sonigo P, Elmaleh A, Fermont L, Delezoide A-L, Mirlesse V, Brunelle F. 1996. Prenatal MRI diagnosis of fetal cerebral tuberous sclerosis. Pediatr Radiol 26: 1-4.
-
(1996)
Pediatr Radiol
, vol.26
, pp. 1-4
-
-
Sonigo, P.1
Elmaleh, A.2
Fermont, L.3
Delezoide, A.-L.4
Mirlesse, V.5
Brunelle, F.6
-
20
-
-
0030879277
-
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34
-
van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Ouweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachatam M, Ravine D, Kwiatkowski DJ, et al. 1997. Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34. Science 277: 805-808.
-
(1997)
Science
, vol.277
, pp. 805-808
-
-
Van Slegtenhorst, M.1
De Hoogt, R.2
Hermans, C.3
Nellist, M.4
Janssen, B.5
Verhoef, S.6
Lindhout, D.7
Van Den Ouweland, A.8
Halley, D.9
Young, J.10
Burley, M.11
Jeremiah, S.12
Woodward, K.13
Nahmias, J.14
Fox, M.15
Ekong, R.16
Osborne, J.17
Wolfe, J.18
Povey, S.19
Snell, R.G.20
Cheadle, J.P.21
Jones, A.C.22
Tachatam, M.23
Ravine, D.24
Kwiatkowski, D.J.25
more..
-
21
-
-
0025234992
-
Tuberous sclerosis presenting with fetal and neonatal cardiac tumours
-
Wallace G, Smith HC, Watson GH, Rimmer S, D'Souza SW. 1990. Tuberous sclerosis presenting with fetal and neonatal cardiac tumours. Arch Dis Child 65: 377-379.
-
(1990)
Arch Dis Child
, vol.65
, pp. 377-379
-
-
Wallace, G.1
Smith, H.C.2
Watson, G.H.3
Rimmer, S.4
D'Souza, S.W.5
-
22
-
-
0028673825
-
Prenatal diagnosis of tuberous sclerosis. Use of magnetic resonance imaging and its implications for prognosis
-
Werner H, Mirlesse V, Jacquemard F, Sonigo P, Delezoide A-L, Gonzales M, Brunelle F, Fermont L, Daffos F. 1994. Prenatal diagnosis of tuberous sclerosis. Use of magnetic resonance imaging and its implications for prognosis. Prenat Diag 14: 1151-1154.
-
(1994)
Prenat Diag
, vol.14
, pp. 1151-1154
-
-
Werner, H.1
Mirlesse, V.2
Jacquemard, F.3
Sonigo, P.4
Delezoide, A.-L.5
Gonzales, M.6
Brunelle, F.7
Fermont, L.8
Daffos, F.9
-
23
-
-
0029124823
-
Alternative splicing of the tuberous sclerosis 2 (TSC2) gene in human and mouse tissues
-
Xu L, Sterner C, Maheshwar MM, Wilson PJ, Nellist M, Short PM, Haines JL, Amesh V. 1995. Alternative splicing of the tuberous sclerosis 2 (TSC2) gene in human and mouse tissues. Genomics 27: 475-480.
-
(1995)
Genomics
, vol.27
, pp. 475-480
-
-
Xu, L.1
Sterner, C.2
Maheshwar, M.M.3
Wilson, P.J.4
Nellist, M.5
Short, P.M.6
Haines, J.L.7
Amesh, V.8
|