-
1
-
-
0030075705
-
The second-trimester fetus with Down syndrome: Detection using sonographic features
-
Benacerraf BR. The second-trimester fetus with Down syndrome: detection using sonographic features. Ultrasound Obstet Gynecol 1996;7:147-55
-
(1996)
Ultrasound Obstet. Gynecol.
, vol.7
, pp. 147-155
-
-
Benacerraf, B.R.1
-
3
-
-
0021821587
-
A sonographic sign for the detection in the second trimester of the fetus with Down's syndrome
-
Benacerraf BR, Barss VA, Laboda LA. A sonographic sign for the detection in the second trimester of the fetus with Down's syndrome. Am J Obstet Gynecol 1985;151:1078-9
-
(1985)
Am. J. Obstet. Gynecol.
, vol.151
, pp. 1078-1079
-
-
Benacerraf, B.R.1
Barss, V.A.2
Laboda, L.A.3
-
4
-
-
0026562612
-
Fetal nuchal translucency screening for chromosomal defects in first trimester of pregnancy
-
Nicolaides KH, Azar G, Byrne D, Mansur C, Marks K. Fetal nuchal translucency screening for chromosomal defects in first trimester of pregnancy. Br Med J 1992;304:867-9
-
(1992)
Br. Med. J.
, vol.304
, pp. 867-869
-
-
Nicolaides, K.H.1
Azar, G.2
Byrne, D.3
Mansur, C.4
Marks, K.5
-
5
-
-
0035961570
-
Second trimester ultrasound to detect fetuses with Down syndrome: A meta analysis
-
Smidt-Bindman R, Hosmer W, Feldstein V, Deeks JJ, Goldberg J. Second trimester ultrasound to detect fetuses with Down syndrome: a meta analysis. J Am Med Assoc 2001;285:1044-55
-
(2001)
J. Am. Med. Assoc.
, vol.285
, pp. 1044-1055
-
-
Smidt-Bindman, R.1
Hosmer, W.2
Feldstein, V.3
Deeks, J.J.4
Goldberg, J.5
-
6
-
-
0032146382
-
UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation
-
Snijders RJM, Noble P, Sebire N, Souka A, Nicolaides KH. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Lancet 1998;352:343-6
-
(1998)
Lancet
, vol.352
, pp. 343-346
-
-
Snijders, R.J.M.1
Noble, P.2
Sebire, N.3
Souka, A.4
Nicolaides, K.H.5
-
7
-
-
0034010666
-
Assessment of risk for chromosomal abnormalities at 10-14 weeks of gestation by nuchal translucency and maternal age in 5210 fetuses carried out at a single center
-
Zoppi MA, Ibba RM, Putzolu M, Floris M, Monni G. Assessment of risk for chromosomal abnormalities at 10-14 weeks of gestation by nuchal translucency and maternal age in 5210 fetuses carried out at a single center. Fetal Diagn Ther 2000;15:170-3
-
(2000)
Fetal Diagn. Ther.
, vol.15
, pp. 170-173
-
-
Zoppi, M.A.1
Ibba, R.M.2
Putzolu, M.3
Floris, M.4
Monni, G.5
-
8
-
-
0034987147
-
Nuchal translucency and the acceptance of invasive prenatal chromosomal diagnosis in women aged 35 and older
-
Zoppi MA, Ibba RM, Putzolu M, Floris M, Monni G. Nuchal translucency and the acceptance of invasive prenatal chromosomal diagnosis in women aged 35 and older. Obstet Gynecol 2001;97:916-20
-
(2001)
Obstet. Gynecol.
, vol.97
, pp. 916-920
-
-
Zoppi, M.A.1
Ibba, R.M.2
Putzolu, M.3
Floris, M.4
Monni, G.5
-
10
-
-
0035682245
-
Relationship between nuchal translucency at 11-14 weeks and nuchal fold at 20-24 weeks of gestation
-
Salomon LJ, Bernard JP, Taupin P, Benard C, Ville Y. Relationship between nuchal translucency at 11-14 weeks and nuchal fold at 20-24 weeks of gestation. Ultrasound Obstet Gynecol 2001;18:636-7
-
(2001)
Ultrasound Obstet. Gynecol.
, vol.18
, pp. 636-637
-
-
Salomon, L.J.1
Bernard, J.P.2
Taupin, P.3
Benard, C.4
Ville, Y.5
-
11
-
-
0029194658
-
Fetal nuchal translucency: A need to understand the physiological basis
-
Moscoso G. Fetal nuchal translucency: a need to understand the physiological basis. Ultrasound Obstet Gynecol 1995;5:6-8
-
(1995)
Ultrasound Obstet. Gynecol.
, vol.5
, pp. 6-8
-
-
Moscoso, G.1
-
13
-
-
0031047257
-
Abnormalities of the heart and great arteries in first trimester chromosomally abnormal fetuses
-
Hyett J, Moscoso G, Nicolaides K. Abnormalities of the heart and great arteries in first trimester chromosomally abnormal fetuses. Am J Med Genet 1997; 17:207-16
-
(1997)
Am. J. Med. Genet.
, vol.17
, pp. 207-216
-
-
Hyett, J.1
Moscoso, G.2
Nicolaides, K.3
-
14
-
-
0034920539
-
Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester
-
Souka AP, Krampl E, Bakalis S, Heath V. Nicolaides KH. Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester. Ultrasound Obstet Gynecol 2001;18:5-8
-
(2001)
Ultrasound Obstet. Gynecol.
, vol.18
, pp. 5-8
-
-
Souka, A.P.1
Krampl, E.2
Bakalis, S.3
Heath, V.4
Nicolaides, K.H.5
-
15
-
-
0031950766
-
Morphological classifiation of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12-18 weeks and in a trisomy 16 mouse
-
von Kaisenberg CS, Krenn V, Ludwig M, Nicolaides KH, Brand Saberi B. Morphological classifiation of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12-18 weeks and in a trisomy 16 mouse. Anat Embryol 1998;197:105-24
-
(1998)
Anat. Embryol.
, vol.197
, pp. 105-124
-
-
von Kaisenberg, C.S.1
Krenn, V.2
Ludwig, M.3
Nicolaides, K.H.4
Brand Saberi, B.5
-
16
-
-
0032032234
-
Collagen type VI gene expression in the skin of trisomy 21 fetuses
-
von Kaisenberg CS, Brand-Saberi B, Christ B, Vallian S, Farzaneh F, Nicolaides KH. Collagen type VI gene expression in the skin of trisomy 21 fetuses. Obstet Gynecol 1998;91:319-23
-
(1998)
Obstet. Gynecol.
, vol.91
, pp. 319-323
-
-
von Kaisenberg, C.S.1
Brand-Saberi, B.2
Christ, B.3
Vallian, S.4
Farzaneh, F.5
Nicolaides, K.H.6
-
17
-
-
0342424307
-
Hyaluronan in the nuchal skin of chromosomally abnormal fetuses
-
Bohlandt S, von Kaisenberg CS, Wewetzler K, Christ B, Nicolaides KH, Brand-Saberi B. Hyaluronan in the nuchal skin of chromosomally abnormal fetuses. Hum Reprod 2000;15:1155-8
-
(2000)
Hum. Reprod.
, vol.15
, pp. 1155-1158
-
-
Bohlandt, S.1
von Kaisenberg, C.S.2
Wewetzler, K.3
Christ, B.4
Nicolaides, K.H.5
Brand-Saberi, B.6
-
18
-
-
0031590497
-
Fetal nuchal translucency test for Down's syndrome
-
Monni G, Zoppi MA, Ibba RM, Floris M. Fetal nuchal translucency test for Down's syndrome. Lancet 1997; 350:1631
-
(1997)
Lancet
, vol.350
, pp. 1631
-
-
Monni, G.1
Zoppi, M.A.2
Ibba, R.M.3
Floris, M.4
-
19
-
-
0035171772
-
Prenatal informed consent for sonogram: The time for first trimester nuchal translucency has come
-
Chasen ST, Skupsi DW, McCullogh LB, Chervenak FA. Prenatal informed consent for sonogram: the time for first trimester nuchal translucency has come. J Ultrasound Med 2001;20:1147-52
-
(2001)
J. Ultrasound Med.
, vol.20
, pp. 1147-1152
-
-
Chasen, S.T.1
Skupsi, D.W.2
McCullogh, L.B.3
Chervenak, F.A.4
-
20
-
-
0032999749
-
A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free β-human chorionic gonadotropin and pregnancy-associated plasma protein-A
-
Spencer K, Souter V, Tul N, Snijders R, Nicolaides K. A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free β-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Ultrasound Obstet Gynecol 1999;13:231-7
-
(1999)
Ultrasound Obstet. Gynecol.
, vol.13
, pp. 231-237
-
-
Spencer, K.1
Souter, V.2
Tul, N.3
Snijders, R.4
Nicolaides, K.5
-
21
-
-
0033549839
-
Integrated screening for Down's syndrome on the basis of test performed during the first and second trimesters
-
Wald NJ, Watt HC, Hackshaw AK. Integrated screening for Down's syndrome on the basis of test performed during the first and second trimesters. N Engl J Med 1999;12:461-7
-
(1999)
N. Engl. J. Med.
, vol.12
, pp. 461-467
-
-
Wald, N.J.1
Watt, H.C.2
Hackshaw, A.K.3
-
22
-
-
0035115234
-
Ductus venosus blood flow in chromosomally abnormal fetuses at 11 to 14 weeks of gestation
-
Matias A, Montenegro N. Ductus venosus blood flow in chromosomally abnormal fetuses at 11 to 14 weeks of gestation. Semin Perinatol 2001;25:32-7
-
(2001)
Semin. Perinatol.
, vol.25
, pp. 32-37
-
-
Matias, A.1
Montenegro, N.2
-
23
-
-
0036156421
-
First trimester ductus venosus velocimetry in relation to nuchal translucency thickness and fetal karyotype
-
Zoppi MA, Putzolu M, Ibba RM, Floris M, Monni G. First trimester ductus venosus velocimetry in relation to nuchal translucency thickness and fetal karyotype. Fetal Diagn Ther 2002;17:52-7
-
(2002)
Fetal. Diagn. Ther.
, vol.17
, pp. 52-57
-
-
Zoppi, M.A.1
Putzolu, M.2
Ibba, R.M.3
Floris, M.4
Monni, G.5
-
24
-
-
0032818728
-
Skeletal abnormalities in fetuses with Down's syndrome: A radiographic post-mortem study
-
Stempfle N, Huten Y, Fredouille C, Brisse H, Nessmann C. Skeletal abnormalities in fetuses with Down's syndrome: a radiographic post-mortem study. Pediatr Radiol 1999;29:682-8
-
(1999)
Pediatr. Radiol.
, vol.29
, pp. 682-688
-
-
Stempfle, N.1
Huten, Y.2
Fredouille, C.3
Brisse, H.4
Nessmann, C.5
-
25
-
-
0024341160
-
Long-bone growth in fetuses with Down syndrome
-
Fitzsimmons J, Droste S, Shepard TH, Pascoe-Mason J, Chinn A, Mack LA. Long-bone growth in fetuses with Down syndrome. Am J Obstet Gynecol 1989; 161:1174-7
-
(1989)
Am. J. Obstet. Gynecol.
, vol.161
, pp. 1174-1177
-
-
Fitzsimmons, J.1
Droste, S.2
Shepard, T.H.3
Pascoe-Mason, J.4
Chinn, A.5
Mack, L.A.6
-
27
-
-
0023711128
-
Sonographic demonstration of hypopolasia of the middle phalanx of the fifth digit, a finding associated with Down syndrome
-
Benacerraf BR, Osathanondh R, Frigoletto FD. Sonographic demonstration of hypopolasia of the middle phalanx of the fifth digit, a finding associated with Down syndrome. Am J Obstet Gynecol 1988; 159:181-3
-
(1988)
Am. J. Obstet. Gynecol.
, vol.159
, pp. 181-183
-
-
Benacerraf, B.R.1
Osathanondh, R.2
Frigoletto, F.D.3
-
28
-
-
0029181484
-
Fifth digit measurement in normal pregnancies, a potential sonographic sign of Down's syndrome
-
Goldstein I, Gomez K, Copel JA. Fifth digit measurement in normal pregnancies, a potential sonographic sign of Down's syndrome. Ultrasound Obstet Gynecol 1995;5:34-7
-
(1995)
Ultrasound Obstet. Gynecol.
, vol.5
, pp. 34-37
-
-
Goldstein, I.1
Gomez, K.2
Copel, J.A.3
-
29
-
-
0015423730
-
Abnormal pelvis in newborn infants with Down's syndrome
-
Mortensson W, Hall B. Abnormal pelvis in newborn infants with Down's syndrome. Acta Radiol 1972; 12:847-55
-
(1972)
Acta Radiol.
, vol.12
, pp. 847-855
-
-
Mortensson, W.1
Hall, B.2
-
30
-
-
0031824167
-
Can fetal iliac bone measurement be used as a marker for Down's syndrome screening?
-
Zoppi MA, Ibba RM, Floris M, Monni G. Can fetal iliac bone measurement be used as a marker for Down's syndrome screening? Ultrasound Obstet Gynecol 1998;12:19-22
-
(1998)
Ultrasound Obstet. Gynecol.
, vol.12
, pp. 19-22
-
-
Zoppi, M.A.1
Ibba, R.M.2
Floris, M.3
Monni, G.4
-
31
-
-
0031015939
-
Pattern of malformations in the axial skeleton in human trisomy 21 fetuses
-
Keeling JW, Fisher Hansen B, Kjaer I. Pattern of malformations in the axial skeleton in human trisomy 21 fetuses. Am J Med Genet 1997;68:466-71
-
(1997)
Am. J. Med. Genet.
, vol.68
, pp. 466-471
-
-
Keeling, J.W.1
Fisher Hansen, B.2
Kjaer, I.3
-
32
-
-
0032545316
-
Pituitary gland and sella turcica in human trisomy 21 fetuses related to axial skeletal development
-
Kjaer I, Keeling JW, Reintoft I, Nolting D, Fisher Hansen B. Pituitary gland and sella turcica in human trisomy 21 fetuses related to axial skeletal development. Am J Med Genet 1998;80:494-500
-
(1998)
Am. J. Med. Genet.
, vol.80
, pp. 494-500
-
-
Kjaer, I.1
Keeling, J.W.2
Reintoft, I.3
Nolting, D.4
Fisher Hansen, B.5
-
35
-
-
0034723733
-
Otocephaly: Prenatal diagnosis of a new case and etiopathogenetic considerations
-
Ibba RM, Zoppi MA, Floris M, et al. Otocephaly: prenatal diagnosis of a new case and etiopathogenetic considerations. Am J Med Genet 2000;90:427-9
-
(2000)
Am. J. Med. Genet.
, vol.90
, pp. 427-429
-
-
Ibba, R.M.1
Zoppi, M.A.2
Floris, M.3
-
36
-
-
0035904786
-
Absence of nasal bone in fetuses with trisomy 21 at 11-14 weeks of gestation: An observational study
-
Cicero S, Curcio P, Papageorghiou A, Sonek J, Nicolaides KH. Absence of nasal bone in fetuses with trisomy 21 at 11-14 weeks of gestation: an observational study. Lancet 2001;358:1665-7
-
(2001)
Lancet
, vol.358
, pp. 1665-1667
-
-
Cicero, S.1
Curcio, P.2
Papageorghiou, A.3
Sonek, J.4
Nicolaides, K.H.5
-
37
-
-
0036153452
-
Prenatal ultrasound diagnosis of nasal bone abnormalities in three fetuses with Down syndrome
-
Sonek J, Nicolaides K. Prenatal ultrasound diagnosis of nasal bone abnormalities in three fetuses with Down syndrome. Am J Obstet Gynecol 2002;186: 139-41
-
(2002)
Am. J. Obstet. Gynecol.
, vol.186
, pp. 139-141
-
-
Sonek, J.1
Nicolaides, K.2
-
38
-
-
0029300823
-
Ultrasound evaluation of the length of the fetal nasal bones throughout gestation
-
Guis F, Ville Y, Vincent Y, Doumerc S, Pons JC, Frydman R. Ultrasound evaluation of the length of the fetal nasal bones throughout gestation. Ultrasound Obstet Gynecol 1995;5:304-7
-
(1995)
Ultrasound Obstet. Gynecol.
, vol.5
, pp. 304-307
-
-
Guis, F.1
Ville, Y.2
Vincent, Y.3
Doumerc, S.4
Pons, J.C.5
Frydman, R.6
-
39
-
-
0036022644
-
Fetal nasal bone length in chromosomally normal and abnormal fetuses at 11-14 weeks of gestation
-
Cicero S, Bindra G, Rembouskos G, Tripsanas C, Nicolaides KH. Fetal nasal bone length in chromosomally normal and abnormal fetuses at 11-14 weeks of gestation. J Maternal Fetal Neonat Med 2002;11: 400-2
-
(2002)
J. Maternal Fetal Neonat. Med.
, vol.11
, pp. 400-402
-
-
Cicero, S.1
Bindra, G.2
Rembouskos, G.3
Tripsanas, C.4
Nicolaides, K.H.5
-
40
-
-
0037070779
-
Absence of nasal bone and detection of trisomy 21
-
Monni G, Zoppi MA, Ibba RM. Absence of nasal bone and detection of trisomy 21. Lancet 2002;359:1343
-
(2002)
Lancet
, vol.359
, pp. 1343
-
-
Monni, G.1
Zoppi, M.A.2
Ibba, R.M.3
-
41
-
-
4243905264
-
Absence of nasal bone and aneuploidies at 11-14 weeks in an unselected population
-
in press
-
Monni G, Zoppi MA, Ibba RM, Floris M, Manca F, Axiana C. Absence of nasal bone and aneuploidies at 11-14 weeks in an unselected population. 2002; in press
-
(2002)
-
-
Monni, G.1
Zoppi, M.A.2
Ibba, R.M.3
Floris, M.4
Manca, F.5
Axiana, C.6
-
42
-
-
0037070931
-
Absence of nasal bone and detection of trisomy 21
-
De Biasio P, Venturini PL. Absence of nasal bone and detection of trisomy 21. Lancet 2002;359:1344
-
(2002)
Lancet
, vol.359
, pp. 1344
-
-
De Biasio, P.1
Venturini, P.L.2
-
43
-
-
0035904768
-
Time for total shift to first trimester screening for Down's syndrome
-
Cuckle H. Time for total shift to first trimester screening for Down's syndrome. Lancet 2001;358:1658-9
-
(2001)
Lancet
, vol.358
, pp. 1658-1659
-
-
Cuckle, H.1
-
44
-
-
0029829691
-
Pattern of malformations in the axial skeleton in human trisomy 18 fetuses
-
Kjaer I, Keeling JW, Fisher Hansen B. Pattern of malformations in the axial skeleton in human trisomy 18 fetuses. Am J Med Genet 1996;65:332-6
-
(1996)
Am. J. Med. Genet.
, vol.65
, pp. 332-336
-
-
Kjaer, I.1
Keeling, J.W.2
Fisher Hansen, B.3
-
46
-
-
0034645516
-
Aspect of skeletal development in fragile X syndrome fetuses
-
Hjalgrim H, Fisher Hansen B, Brondum-Nielsen K, Nolting D, Kjaer I. Aspect of skeletal development in fragile X syndrome fetuses. Am J Med Genet 2000; 95:123-9
-
(2000)
Am. J. Med. Genet.
, vol.95
, pp. 123-129
-
-
Hjalgrim, H.1
Fisher Hansen, B.2
Brondum-Nielsen, K.3
Nolting, D.4
Kjaer, I.5
|