Works matching IS 01973851 AND DT 2009 AND VI 29 AND IP 6

Results: 19

Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different alpha 0-thalassemia defects in China.

Published in:

2009

By:

Li DZ;
Li J;
Liao C;
Li, Dong-Zhi;
Li, Jian;
Liao, Can

Publication type:

Case Study

The impact of fetal gender on first trimester nuchal translucency and maternal serum free beta-hCG and PAPP-A MoM in normal and trisomy 21 pregnancies.

Published in:

2009

By:

Cowans NJ;
Stamatopoulou A;
Maiz N;
Spencer K;
Nicolaides KH;
Cowans, Nicholas J;
Stamatopoulou, Anastasia;
Maiz, Nerea;
Spencer, Kevin;
Nicolaides, Kypros H

Publication type:

journal article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 2009, v. 29, n. 6, p. 639, doi. 10.1002/pd.2099
Publication type:: Article

First-trimester maternal serum matrix metalloproteinase-9 (MMP-9) and adverse pregnancy outcome.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 553, doi. 10.1002/pd.2234

By:

Poon, Leona C. Y.;
Nekrasova, Ekaterina;
Anastassopoulos, Panagiotis;
Livanos, Panagiotis;
Nicolaides, Kypros H.

Publication type:

Article

Antibiotic Prophylaxis before second-trimester Genetic Amniocentesis (APGA): a single-centre open randomised controlled trial.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 606, doi. 10.1002/pd.2256

By:

Giorlandino, Claudio;
Cignini, Pietro;
Cini, Marco;
Brizzi, Cristiana;
Carcioppolo, Ornella;
Milite, Vincenzo;
Coco, Claudio;
Gentili, Paolo;
Mangiafico, Lucia;
Mesoraca, Alvaro;
Bizzoco, Domenico;
Gabrielli, Ivan;
Mobili, Luisa

Publication type:

Article

Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 560, doi. 10.1002/pd.2238

By:

Chung, Wendy;
Winder, Thomas L.;
LeDuc, Charles A.;
Simpson, Lynn L.;
Millar, William S.;
Dungan, Jeffrey;
Ginsberg, Norman;
Plaga, Stacey;
Moore, Steven A.;
Chung, Wendy K.

Publication type:

Article

In vitro evaluation of the ability of platelet-rich plasma to seal an iatrogenic fetal membrane defect.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 620, doi. 10.1002/pd.2249

By:

Lewi, L.;
Liekens, D.;
Heyns, L.;
Poliard, E.;
Beutels, E.;
Deprest, J.;
Hoylaerts, M. F.

Publication type:

Article

The role of echocardiography in prenatal diagnosis of pulmonary arteriovenous malformation.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 634, doi. 10.1002/pd.2261

By:

Sinkovskaya, Elena;
Berkley, Eliza;
Bogdan, Donna;
Sclater, Annette;
Abuhamad, Alfred

Publication type:

Article

Premarital screening for thalassemia in mainland China.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 637, doi. 10.1002/pd.2251

By:

Li, Dong-Zhi

Publication type:

Article

Amniocentesis in the second trimester and congenital talipes equinovarus in the offspring: a population-based record linkage study in Scotland.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 613, doi. 10.1002/pd.2233

By:

Cardy, A. H.;
Torrance, N.;
Clark, D.;
Miedzybrodzka, Z.;
Sharp, L.

Publication type:

Article

Attitudes of Chinese couples in Hong Kong regarding using preimplantation genetic diagnosis (PGD) and human leukocyte antigens (HLA) typing to conceive a 'Saviour Child'.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 593, doi. 10.1002/pd.2255

By:

Hui, Edwin C.;
Chan, Carina;
Liu, Athena;
Chow, Kathy

Publication type:

Article

Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different α<sup>0</sup>-thalassemia defects in China.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 632, doi. 10.1002/pd.2259

By:

Li, Dong-Zhi;
Li, Jian;
Liao, Can

Publication type:

Article

A case of congenital lymphocytic choriomeningitis virus (LCMV) infection revealed by hydrops fetalis.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 626, doi. 10.1002/pd.2240

By:

Meritet, J. F.;
Krivine, A.;
Lewin, F.;
Poissonnier, M. H.;
Poizat, R.;
Loget, P.;
Rozenberg, F.;
Lebon, P.

Publication type:

Article

Performance of first-trimester combined screening for trisomy 13 and 18 with the double test taken at a gestational age of 8 + 0 to 13 + 6.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 582, doi. 10.1002/pd.2254

By:

Kirkegaard, Ida;
Petersen, Olav Bjørn;
Uldbjerg, Niels;
Tørring, Niels

Publication type:

Article

ADAM12 in first trimester maternal serum from pregnancies conceived by assisted reproduction techniques (ART).

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 628, doi. 10.1002/pd.2180

By:

Laigaard, Jennie;
Gros Pedersen, Nina;
Olesen Larsen, Severin;
Hedley, Paula Louise;
Wøjdemann, Karen;
Gjerris, Anne Cathrine;
Shalmi, Anne-Cathrine;
Sundberg, Karin;
Tabor, Ann;
Christiansen, Michael

Publication type:

Article

First-trimester Down syndrome screening performance in the Dutch population; how to achieve further improvement?

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 588, doi. 10.1002/pd.2247

By:

Wortelboer, E. J.;
Koster, M. P. H.;
Stoutenbeek, Ph.;
Elvers, L. H.;
Loeber, J. G.;
Visser, G. H. A.;
Schielen, P. C. J. I.

Publication type:

Article

Management of pregnancy in a carrier of the Donohue mutation.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 630, doi. 10.1002/pd.2253

By:

Penninx, J. P. M.;
Vinken, P. G. C.;
Porath, M. M.

Publication type:

Article

The impact of fetal gender on first trimester nuchal translucency and maternal serum free β-hCG and PAPP-A MoM in normal and trisomy 21 pregnancies.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 578, doi. 10.1002/pd.2246

By:

Cowans, Nicholas J.;
Stamatopoulou, Anastasia;
Maiz, Nerea;
Spencer, Kevin;
Nicolaides, Kypros H.

Publication type:

Article

Identification of second trimester screen positive pregnancies at increased risk for congenital heart defects.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 570, doi. 10.1002/pd.2239

By:

Jelliffe-Pawlowski, Laura L.;
Walton-Haynes, Lynn;
Currier, Robert J.

Publication type:

Article