Works matching IS 01973851 AND DT 2005 AND VI 25 AND IP 6

Results: 26

Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 523, doi. 10.1002/pd.1182

By:

Chen, Chih-Ping;
Liu, Yu-Peng;
Huang, Jon-Kway;
Chang, Tung-Yao;
Chen, Ming-Ren;
Chiu, Nan-Chang;
Wang, Wayseen

Publication type:

Article

First-trimester screening for fetal triploidy at 11 to 14 weeks: a role for fetal biometry.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 479, doi. 10.1002/pd.1170

By:

Salomon, L. J.;
Bernard, J. P.;
Nizard, J.;
Ville, Y.

Publication type:

Article

Which contingent sequential screening protocol?

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 520, doi. 10.1002/pd.1147

By:

Wright, Dave;
Bradbury, Ian;
Benn, Peter;
Cuckle, Howard;
Ritchie, Karen

Publication type:

Article

Fetal size charts for the Italian population. Normative curves of head, abdomen and long bones.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 456, doi. 10.1002/pd.1158

By:

Paladini, Dario;
Rustico, Mariangela;
Viora, Elsa;
Giani, Umberto;
Bruzzese, Dario;
Campogrande, Mario;
Martinelli, Pasquale

Publication type:

Article

Prenatal imaging of limb-body wall complex by magnetic resonance imaging.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 521, doi. 10.1002/pd.838

By:

Chen, Chih-Ping;
Cheng, Sho-Jen;
Lin, Yi-Hui;
Wang, Wayseen

Publication type:

Article

Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 492, doi. 10.1002/pd.1179

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Wang, Tzu-Hao;
Hsueh, Ding-Wei;
Lee, Chen-Chi;
Town, Dai-Dyi;
Wang, Wayseen;
Ko, Tsang-Ming

Publication type:

Article

The prenatal multiplier method for prediction of limb length discrepancy.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 435, doi. 10.1002/pd.1113

By:

Paley, Jonathan;
Gelman, Amanda;
Paley, Dror;
Herzenberg, John E

Publication type:

Article

Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 470, doi. 10.1002/pd.1164

By:

Peng, Hsiu-Huei;
Wang, Tzu-Hao;
Hsueh, Ding-Wei;
Chang, Shuenn-Dyh;
Soong, Yung-Kuei

Publication type:

Article

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 502, doi. 10.1002/pd.1181

By:

Chen, Chih-Ping;
Chern, Schu-Rern;
Sheu, Jin-Chern;
Lin, Shuan-Pei;
Hsu, Chin-Yuan;
Chang, Tung-Yao;
Lee, Chen-Chi;
Wang, Wayseen;
Cindy Chen, Hsiao-En

Publication type:

Article

Fetal nasal bone and trisomy 21 in the second trimester.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 511, doi. 10.1002/pd.848

By:

Viora, E.;
Errante, G.;
Sciarrone, A.;
Bastonero, S.;
Masturzo, B.;
Martiny, G.;
Campogrande, M.

Publication type:

Article

Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRI.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 442, doi. 10.1002/pd.1145

By:

Doherty, Dan;
Glass, Ian A.;
Siebert, Joseph R.;
Strouse, Peter J.;
Parisi, Melissa A.;
Shaw, Dennis W. W.;
Chance, Phillip F.;
Barr, Mason;
Nyberg, David

Publication type:

Article

Prospective audit of a one-centre combined nuchal translucency and triple test programme for the detection of trisomy 21.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 465, doi. 10.1002/pd.1163

By:

Babbur, Vijayalakshmi;
Lees, Christoph C.;
Goodburn, Sandra F.;
Morris, Nigel;
Breeze, Andrew C. G.;
Hackett, Gerald A.

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2005, v. 25, n. 6, p. 529, doi. 10.1002/pd.1020
Publication type:: Article

Frontal bilateral megalencephaly: fetal and autopsy MR evaluation of an unclassified malformation.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 489, doi. 10.1002/pd.1178

By:

Parazzini, Cecilia;
Righini, Andrea;
Lalatta, Faustina;
Bianchini, Elena;
Triulzi, Fabio

Publication type:

Article

Silver-Russell syndrome as a cause for early intrauterine growth restriction.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 497, doi. 10.1002/pd.1180

By:

Falkert, Andreas;
Dittmann, Kai;
Seelbach-Göbel, Birgit

Publication type:

Article

Perinatal findings of partial trisomy 13q (13q14.1→qter) resulting from paternal pericentric inversion of chromosome 13.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 527, doi. 10.1002/pd.1177

By:

Chen, Chih-Ping;
Lin, Shuan-Pei;
Lee, Chen-Chi;
Chen, Wen-Lin;
Chen, Li-Feng;
Wang, Wayseen

Publication type:

Article

Sonographic features of lethal multiple pterygium syndrome at 14 weeks.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 475, doi. 10.1002/pd.1166

By:

Chen, Min;
Chan, Gavin Shueng Wai;
Lee, Chin Peng;
Tang, Mary Hoi Yin

Publication type:

Article

Survey on the future organisation of first-trimester ultrasound screening in Flanders, Belgium.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 518, doi. 10.1002/pd.1137

By:

Gyselaers, Wilfried;
De Catte, Luc;
Witters, Ingrid;
de Jonge, Eric;
Ombelet, Willem;
Nijhuis, Jan

Publication type:

Article

46,XY,18q+/46,XY,18q− mosaicism in a fragile X prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 448, doi. 10.1002/pd.1150

By:

Rodriguez-Revenga, Laia;
Badenas, Celia;
Madrigal, Irene;
Sánchez, Aurora;
Soler, Anna;
Carrió, Ana;
Milà, Montserrat

Publication type:

Article

Congenital cervical teratoma, associated with agenesis of corpus callosum and a subarachnoid cyst.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 439, doi. 10.1002/pd.1056

By:

Goldstein, Israel;
Drugan, Arie

Publication type:

Article

Fetal lateral neck cysts: the significance of associated findings.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 507, doi. 10.1002/pd.1161

By:

Sharony, Reuven;
Tepper, Ronnie;
Fejgin, Moshe

Publication type:

Article

Reversible absent/reversed end-diastolic flow in the umbilical artery, and reversible brain-sparing effect in a case with umbilical cord entanglement.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 516, doi. 10.1002/pd.868

By:

Leeners, Brigitte;
Sauer, Itta;
Funk, Andreas;
Rath, Werner

Publication type:

Article

Osteogenesis imperfecta associated with first-trimester ventriculomegaly as an early ultrasound sign.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 519, doi. 10.1002/pd.1143

By:

Cho, Fu-Nan;
Kan, Yuen-Yee;
Chen, San-Nung;
Yang, Tsung-lung;
Hsu, Pei-Hua

Publication type:

Article

Prenatal magnetic resonance imaging of Galloway-Mowat syndrome.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 525, doi. 10.1002/pd.1183

By:

Chen, Chih-Ping;
Chang, Tung-Yao;
Lin, Shuan-Pei;
Huang, Jon-Kway;
Tsai, Jeng-Daw;
Chiu, Nan-Chang;
Wang, Wayseen

Publication type:

Article

Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 451, doi. 10.1002/pd.1154

By:

Beaujard, M.-P.;
Jouannic, J.-M.;
Bessières, B.;
Borie, C.;
Martin-Luis, I.;
Fallet-Bianco, C.;
Portnoï, M.-F.

Publication type:

Article

Weight adjustment of serum markers in early first-trimester prenatal screening for Down syndrome.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 484, doi. 10.1002/pd.1176

By:

Sørensen, Tina;
Larsen, Severin Olesen;
Christiansen, Michael

Publication type:

Article