Works matching DE "GENETIC disorders in pregnancy"

Results: 86

A Comparison of the performance of Invasive Tests for Genetic Congenital Defects in Response of the First- Trimester Screening with High and High Moderate Risks.

Published in:

International Journal of Pharmaceutical Research & Allied Sciences, 2016, v. 5, n. 2, p. 103

By:

Mohammadjafari, Raziye;
Zarei, Leili;
Shahbaziyan, Nahid;
Barati, Mojgan;
Moramezi, Farideh;
Hemadi, Masoud

Publication type:

Article

P11.17: Prenatal diagnosis of ring chromosome 18.

Published in:

Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 247, doi. 10.1002/uog.14208

By:

Al Nasiry, S.;
Willekes, C.;
Pieters, M.;
Coumans, A.;
Witters, I.

Publication type:

Article

P02.13: Transcervical chorionic villous sampling: experience in a private centre in Spain.

Published in:

Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 192, doi. 10.1002/uog.14023

By:

Illescas, T.;
Adiego, B.;
Martínez-Ten, P.

Publication type:

Article

OP01.01: Prevalence, clinical impact and recurrence risk of genetic disorders in prenatal medicine: lessons from our unit over 15 years.

Published in:

Ultrasound in Obstetrics & Gynecology, 2013, v. 42, p. 48, doi. 10.1002/uog.12715

By:

Schroeer, A.;
Brandt, P.;
Hartge, D. R.;
Weichert, J.

Publication type:

Article

Nuchal translucency and cystic hygroma colli in screening for fetal major congenital heart defects in a series of 12 910 euploid pregnancies.

Published in:

Ultrasound in Obstetrics & Gynecology, 2010, v. 35, n. 3, p. 273, doi. 10.1002/uog.7534

By:

Sananes, N.;
Guigue, V;
Kohler, M.;
Bouffet, N.;
Cancellier, M.;
Hornecker, F.;
Hunsinger, M. C.;
Kohler, A.;
Mager, C.;
Neumann, M.;
Schmerber, E.;
Tanghe, M.;
Nisand, I.;
Favre, R.

Publication type:

Article

Early second-trimester diagnosis of intracranial teratoma.

Published in:

Ultrasound in Obstetrics & Gynecology, 2009, v. 33, n. 1, p. 109, doi. 10.1002/uog.6231

By:

Saada, J.;
Enza-Razavi, F.;
Delahaye, S.;
Martinovic, J.;
Macaleese, J.;
Benachi, A.

Publication type:

Article

Prenatal diagnosis of Bardet–Biedl syndrome by targeted second-trimester sonography.

Published in:

Ultrasound in Obstetrics & Gynecology, 2001, v. 17, n. 4, p. 354, doi. 10.1046/j.1469-0705.2001.00253.x

By:

Dar, P.;
Sachs, G. S.;
Carter, S. M.;
Ferreira, J. C.;
Nitowsky, H. M.;
Gross, S. J.

Publication type:

Article

Serial sonographic findings in a fetus with congenital hiatal hernia.

Published in:

Ultrasound in Obstetrics & Gynecology, 2001, v. 17, n. 4, p. 350, doi. 10.1046/j.1469-0705.2001.00366.x

By:

Ogunyemi, D.

Publication type:

Article

Prenatal diagnosis of umbilical cord aneurysm in a fetus with trisomy 18.

Published in:

Ultrasound in Obstetrics & Gynecology, 2001, v. 17, n. 1, p. 79, doi. 10.1046/j.1469-0705.2001.00313.x

By:

Berg, C.;
Geipel, A.;
Germer, U.;
Gloeckner-Hofmann, K.;
Gembruch, U.

Publication type:

Article

Letter: A case of achondrogenesis type II associated with huge cystic hygroma: prenatal diagnosis by ultrasonography.

Published in:

1999

By:

Won, H.S.;
Yoo, H.K.;
Lee, P. R.;
Lee, I.S.;
Kim, A.;
Nam, J. H.;
Mok, J. E.

Publication type:

Letter

Mid-trimester amniotic fluid leptin concentration and fetal leptin gene polymorphism: maternal, fetal and pregnancy outcome parameters.

Published in:

2008

By:

Predanic, Mladen;
Perni, Sriram C.;
Jean-Pierre, Claudel C.;
Linhares, Iara M.;
Witkin, Steven S.

Publication type:

Abstract

A Case of Antenatal Bartter Syndrome with Sensorineural Deafness.

Published in:

2010

By:

Lee, Hyun Seung;
Cheong, Hae Il;
Ki, Chang-Seok

Publication type:

Case Study

Session 4: Child Health.

Published in:: West Indian Medical Journal, 2008, v. 57, n. S4, p. 30
Publication type:: Article

A FUNCTIONAL PROMOTER POLYMORPHISM WITHIN MTHFD1 MAY INCREASE NEURAL TUBE DEFECT RISK IN THE IRISH POPULATION THROUGH AN INTERACTION WITH THE R653Q POLYMORPHISM.

Published in:

Ulster Medical Journal, 2009, v. 78, n. 1, p. 67

By:

Carroll, Nicola;
Pangilinan, Faith;
Molloy, Anne M.;
Troendle, James;
Mills, James L.;
Kirke, Peadar N.;
Brody, Lawrence C.;
Scott, John M.;
Parle-McDermott, Anne

Publication type:

Article

First use of preimplantation genotyping in prevention of recurrent diandric complete hydatidiform mole.

Published in:

2009

By:

Ogilvie, C. Mackie;
Renwick, P. J.;
Khalaf, Y.;
Braude, P. R.

Publication type:

Case Study

Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2009, v. 18, n. 4, p. 543, doi. 10.1016/S1472-6483(10)60132-0

By:

De la Fuente-Cortés, Beatriz E.;
Cerda-Flores, Ricardo M.;
Dávila-Rodríguez, Martha I.;
García-Vielma, Catalina;
Alvarado, Rosa M. De la Rosa;
Cortés-Gutiérrez, Elva I.

Publication type:

Article

Self-report versus medical record - perinatal factors in a study of infant leukaemia: a study from the Children's Oncology Group.

Published in:

2011

By:

Jurek, Anne M.;
Greenland, Sander;
Spector, Logan G.;
Roesler, Michelle A.;
Robison, Leslie L.;
Ross, Julie A.

Publication type:

journal article

Diagnosis of Congenital Anomalies during Routine Fetal Surveillance.

Published in:

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2015, v. 9, n. 2, p. 159, doi. 10.5005/jp-journals-10009-1402

By:

Sylejmani, Selami;
Syla, Bajram;
Shala, Sebahate

Publication type:

Article

Management of Multiple Pregnancy.

Published in:

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2009, v. 3, n. 3, p. 45

By:

Dudenhausen, Joachim W.

Publication type:

Article

Umbilicus as a fitness signal in humans.

Published in:

2009

By:

Sinkkonen, Aki

Publication type:

Essay

Association between von Willebrand factor gene polymorphism and preeclampsia.

Published in:

Journal of Perinatal Medicine, 2009, v. 37, n. 1, p. 36, doi. 10.1515/JPM.2009.018

By:

Sun, Chengjuan;
Chen, Ying;
Zhang, Weiyuan;
Yu, Song

Publication type:

Article

Non-invasive prenatal measurement of the fetal genome.

Published in:

Nature, 2012, v. 487, n. 7407, p. 320, doi. 10.1038/nature11251

By:

Fan, H. Christina;
Gu, Wei;
Wang, Jianbin;
Blumenfeld, Yair J.;
El-Sayed, Yasser Y.;
Quake, Stephen R.

Publication type:

Article

Maternal hemoglobin level and birth outcomes in pregnant adolescents.

Published in:

Scientific Journal of Iranian Blood Transfusion Organization, 2013, v. 9, n. 4, p. 455

By:

Alizadeh, L.;
Salehi, L.;
Ramzi, M.

Publication type:

Article

Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family.

Published in:

2012

By:

Kedar, Prabhakar;
Warang, Prashant;
Ghosh, Kanjaksha;
Colah, Roshan

Publication type:

Letter

Anagrelide therapy in pregnancy: report of a case of essential thrombocythemia.

Published in:

2004

By:

Doubek, Michael;
Brychtova, Yvona;
Doubek, Radan;
Janku, Petr;
Mayer, Jiri

Publication type:

Case Study

Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care.

Published in:

European Journal of Endocrinology, 2011, v. 164, n. 2, p. 309, doi. 10.1530/EJE-10-0679

By:

Helton Estrela Ramos

Publication type:

Article

Use of Maternal GHb Concentration to Estimate the Risk of Congenital Anomalies in the Offspring of Women with Prepregnancy Diabetes.

Published in:

Diabetes Care, 2007, v. 30, n. 7, p. 1920, doi. 10.2337/dc07-0278

By:

Guerin, Andrea;
Nisenbaum, Rosane;
Ray, Joel G.

Publication type:

Article

Feasibility of introducing genetic services in the National Family Welfare Programme in India.

Published in:

Indian Journal of Medical Research, 2009, v. 130, n. 4, p. 404

By:

Rasaily, Reeta

Publication type:

Article

Easy on the Vitamin A.

Published in:

Family Planning Perspectives, 1996, v. 28, n. 2, p. 42

By:

Hollander, Dore

Publication type:

Article

Noninvasive Genetic Testing.

Published in:: Family Planning Perspectives, 1990, v. 22, n. 5, p. 197
Publication type:: Article

Pregnancy-associated diseases are characterized by the composition of the systemic regulatory T cell (T<sub>reg</sub>) pool with distinct subsets of T<sub>regs</sub>.

Published in:

Clinical & Experimental Immunology, 2012, v. 167, n. 1, p. 84, doi. 10.1111/j.1365-2249.2011.04493.x

By:

Steinborn, A.;
Schmitt, E.;
Kisielewicz, A.;
Rechenberg, S.;
Seissler, N.;
Mahnke, K.;
Schaier, M.;
Zeier, M.;
Sohn, C.

Publication type:

Article

Acute myeloid leukemia in the pregnant patient.

Published in:

European Journal of Haematology, 2015, v. 95, n. 2, p. 124, doi. 10.1111/ejh.12479

By:

Thomas, Xavier

Publication type:

Article

Avascular Villi, Increased Syncytial Knots, and Hypervascular Villi Are Associated with Pregnancies Complicated by Factor V Leiden Mutation.

Published in:

Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 341, doi. 10.2350/09-05-0657-OA.1

By:

Rogers, Beverly Barton;
Momirova, Valerija;
Dizon-Townson, Donna;
Wenstrom, Katharine;
Samuels, Philip;
Sibai, Baha;
Spong, Catherine;
Caritis, Steve N.;
Sorokin, Yoram;
Miodovnik, Menachem;
O'Sullivan, Mary J.;
Conway, Deborah;
Wapner, Ronald J.

Publication type:

Article

Pregnancy and postpartum specifics in women with schizophrenia: a meta-study.

Published in:

Archives of Gynecology & Obstetrics, 2011, v. 283, n. 2, p. 141, doi. 10.1007/s00404-010-1706-8

By:

Matevosyan, Naira

Publication type:

Article

A meta-analysis of eNOS and ACE gene polymorphisms and risk of pre-eclampsia in women.

Published in:

Journal of Obstetrics & Gynaecology, 2011, v. 31, n. 7, p. 603, doi. 10.3109/01443615.2011.598971

By:

Shaik, A. P.;
Sultana, A.;
Bammidi, V. K.;
Sampathirao, K.;
Jamil, K.

Publication type:

Article

A pregnant woman with genetic variants of butyrylcholinesterase and inflammatory bowel disease.

Published in:

2006

By:

Futagami, M.;
Sakamoto, T.;
Sakamoto, A.;
Shigetou, T.;
Taniguchi, R.;
Sato, S.;
Tutaya, S.;
Kojima, K.;
Yasujima, M.;
Mizunuma, H.

Publication type:

Case Study

Do the MTHFR gene polymorphism and Down syndrome pregnancy association stands true? A case-control study of Indian population and meta-analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 87, doi. 10.1016/j.ejmhg.2015.08.003

By:

Muthuswamy, Srinivasan;
Agarwal, Sarita

Publication type:

Article

Congenital anonychia: A variant of Cook's syndrome.

Published in:

Journal of Chinese Clinical Medicine, 2009, v. 4, n. 10, p. 596

By:

Padmavathy, L.;
Kathimathi, B.;
Rao, L. Lakshmana

Publication type:

Article

Transgenerational Effect of Neighborhood Poverty on Low Birth Weight Among African Americans in Cook County, Illinois.

Published in:

American Journal of Epidemiology, 2009, v. 169, n. 6, p. 712, doi. 10.1093/aje/kwn402

By:

James W. Collins;
Richard J. David;
Kristin M. Rankin;
Jennifer R. Desireddi

Publication type:

Article

Population-based estimate of sibling risk for preterm birth, preterm premature rupture of membranes, placental abruption and pre-eclampsia.

Published in:

BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-44

By:

Plunkett, Jevon;
Borecki, Ingrid;
Morgan, Thomas;
Stamilio, David;
Muglia, Louis J.

Publication type:

Article

Mechanisms of progesterone action in inhibiting prematurity.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2006, v. 19, n. 12, p. 763, doi. 10.1080/14767050600949829

By:

Sfakianaki, Anna K.;
Norwitz, Errol R.

Publication type:

Article

CAN DES RISK BE PASSED ON?

Published in:: Perspectives on Sexual & Reproductive Health, 2006, v. 38, n. 4, p. 181
Publication type:: Article

Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 4, p. 296, doi. 10.1038/jhg.2011.7

By:

Miura, Kiyonori;
Higashijima, Ai;
Shimada, Takako;
Miura, Shoko;
Yamasaki, Kentaro;
Abe, Shuhei;
Jo, Ozora;
Kinoshita, Akira;
Yoshida, Atsushi;
Yoshimura, Shuichiro;
Niikawa, Norio;
Yoshiura, Koh-ichiro;
Masuzaki, Hideaki

Publication type:

Article

The 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene is associated with severe preeclampsia.

Published in:

Journal of Human Genetics, 2000, v. 45, n. 3, p. 138, doi. 10.1007/s100380050200

By:

Yamada, N.;
Arinami, T.;
Yamakawa-Kobayashi, K.;
Watanabe, H.;
Sohda, S.;
Hamada, H.;
Kubo, T.;
Hamaguchi, H.

Publication type:

Article

Hyperlipidemia and pancreatitis during pregnancy in two sisters with a mutation in the lipoprotein..

Published in:

Annals of Internal Medicine, 1996, v. 124, n. 4, p. 425, doi. 10.7326/0003-4819-124-4-199602150-00007

By:

Keilson, Leonard M.;
Vary, Calvin P.H.

Publication type:

Article

Congenital intrathoracic kidney with right Bochdalek defect.

Published in:

2006

By:

Obatake, Masayuki;
Nakata, Tetsuo;
Nomura, Masahito;
Nanashima, Atsushi;
Inamura, Yukio;
Tanaka, Kenji;
Nagayasu, Takeshi

Publication type:

journal article

Study of Association Between Hypertensive Disorders of Pregnancy and the Human Coagulation Factor XI Gene.

Published in:

Hypertension in Pregnancy, 2006, v. 25, n. 1, p. 21, doi. 10.1080/10641950500543863

By:

Sato, Ichiro;
Nakayama, Tomohiro;
Maruyama, Aya;
Furuya, Kiyohide;
Sato, Naoyuki;
Mizutani, Yoshihiro;
Yamamoto, Tatsuo

Publication type:

Article

The effect of the CYP1A2 *1F mutation on CYP1A2 inducibility in pregnant women.

Published in:

British Journal of Clinical Pharmacology, 2002, v. 54, n. 5, p. 504, doi. 10.1046/j.1365-2125.2002.01673.x

By:

Nordmark, Anna;
Lundgren, Stefan;
Ask, Birgitta;
Granath, Fredrik;
Rane, Anders

Publication type:

Article

Atelencephalic Microcephaly.

Published in:

Clinical Pediatrics, 1984, v. 23, n. 11, p. 649, doi. 10.1177/000992288402301110

By:

Alan Shewmon, D.;
Sherman, Michael P.;
Danner, Rolf

Publication type:

Article

Occurrence of Neural Tube Defects in Pregnancy: An Excess of Cases in a 2773-km2 Area in Central Italy.

Published in:

Journal of Toxicology & Environmental Health: Part A, 2008, v. 71, n. 15, p. 981, doi. 10.1080/15287390701838531

By:

Prospero, Emilia;
Barbadoro, Pamela;
Filippetti, Fabio;
Appignanesi, Remo;
Ciavattini, Andrea;
Carle, Flavia

Publication type:

Article