Works matching DE "GENETIC disorders in pregnancy"

Results: 86

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

The analysis of amniocentesis results of pregnants who are at 16-22 weeks of gestation and undergone genetic amniocentesis.

Published in:

Perinatal Journal / Perinatoloji Dergisi, 2013, v. 21, n. 3, p. 101, doi. 10.2399/prn.13.0213001

By:

Timur, Alev;
Uyar, İbrahim;
Gülhan, İbrahim;
Tan Saz, Nagehan;
İleri, Alper;
Özeren, Mehmet

Publication type:

Article

Bioinformatic analysis of computational identified differentially expressed genes in tumor stoma of pregnancy‑associated breast cancer.

Published in:

Molecular Medicine Reports, 2017, v. 16, n. 3, p. 3345, doi. 10.3892/mmr.2017.6947

By:

QIAN ZHOU;
ERHU SUN;
LIJUN LING;
XIAOFENG LIU;
MIN ZHANG;
HONG YIN;
CHENG LU

Publication type:

Article

Session 4: Child Health.

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

Safety and efficacy of lactoferrin versus ferrous sulphate in curing iron deficiency and iron deficiency anaemia in hereditary thrombophilia pregnant women: an interventional study.

Published in:

BioMetals, 2014, v. 27, n. 5, p. 999, doi. 10.1007/s10534-014-9723-x

By:

Paesano, Rosalba;
Pacifici, Enrica;
Benedetti, Samanta;
Berlutti, Francesca;
Frioni, Alessandra;
Polimeni, Antonella;
Valenti, Piera

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

No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.

Published in:

Journal of Gastroenterology & Hepatology, 2007, v. 22, n. 12, p. 2107, doi. 10.1111/j.1440-1746.2006.04682.x

By:

Xiao-Fei Kong;
Xin-Xin Zhang;
Ying-Yan Yu;
Qing Shi;
Duan-Duan La;
Chuan-De Zhu-Ge;
Deng, Lin;
Qi-Ming Gong;
Bai-Yong Shen;
Cheng-Hong Peng;
Hong-Wei Li

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

Maternal imprinting defect.

Published in:

Nature Genetics, 2011, v. 43, n. 10, p. 928, doi. 10.1038/ng.967

By:

Vogan, Kyle

Publication type:

Article

Pregnancy immunogenetics: NK cell education in the womb?

Published in:

2010

By:

Parham, Peter;
Guethlein, Lisbeth A.

Publication type:

journal article

Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2.

Published in:

2010

By:

Hiby, Susan E.;
Apps, Richard;
Sharkey, Andrew M.;
Farrell, Lydia E.;
Gardner, Lucy;
Mulder, Arend;
Claas, Frans H.;
Walker, James J.;
Redman, Christopher C.;
Morgan, Linda;
Tower, Clare;
Regan, Lesley;
Moore, Gudrun E.;
Carrington, Mary;
Moffett, Ashley;
Redman, Christopher W

Publication type:

journal 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

Prenatal genetic diagnosis of Neu-Laxova syndrome.

Published in:

2018

By:

Wood, Amber M.;
Mottola, Amy T.;
Rhee, Eleanor H.;
Kuller, Jeffrey A.

Publication type:

journal article

Expression of insulin-like growth factor-I and placental growth hormone mRNA in placentae: a comparison between normal and intrauterine growth retardation pregnancies.

Published in:

Molecular Human Reproduction, 2001, v. 7, n. 3, doi. 10.1093/molehr/7.3.287

By:

Sheikh, Shamim;
Satoskar, Purnima;
Bhartiya, Deepa

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

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

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

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

Risk of obstetric cholestasis in sisters of index patients.

Published in:

Clinical Genetics, 2001, v. 60, n. 1, p. 42, doi. 10.1034/j.1399-0004.2001.600106.x

By:

Eloranta, M-L;
Heinonen, S;
Mononen, T;
Saarikoski, S

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

The clinical utility of genetic testing of tissues from pregnancy losses.

Published in:

2018

By:

Waterman, C. A.;
Batstone, P.;
Bown, N.;
Cresswell, L.;
Delmege, C.;
English, C. J.;
Fews, G.;
Grimsley, L.;
Imrie, S.;
Kulkarni, A.;
Mann, K.;
Johnson, R.;
Morgan, S. M.;
Roberts, P.;
Simonic, I.;
Trueman, S.;
Wall, M.;
McMullan, D.

Publication type:

journal article

Management of Inherited Bleeding Disorders in Pregnancy: Green-top Guideline No. 71 (joint with UKHCDO).

Published in:: 2017
Publication type:: journal article

CAN DES RISK BE PASSED ON?

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

Management of pregnancy, labour and delivery in women with inherited bleeding disorders.

Published in:

Haemophilia, 2011, v. 17, p. 20, doi. 10.1111/j.1365-2516.2011.02561.x

By:

HUQ, F. Y.;
KADIR, R. A.

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

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

The Adverse Effects of Pregnancies Complicated by Hemoglobin H (HBH) Disease.

Published in:

2015

By:

Rabiee, Maryam;
Shams, Jalal-Aldin;
Zafargandie, Nafiseh

Publication type:

Case Study

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

New KRT10 gene mutation underlying the annular variant of bullous congenital ichthyosiform erythroderma with clinical worsening during pregnancy.

Published in:

British Journal of Dermatology, 2007, v. 157, n. 3, p. 602, doi. 10.1111/j.1365-2133.2007.08054.x

By:

Sheth, N.;
Greenblatt, D.;
McGrath, J.A.

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

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

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

Circulating Maternal Total Cell-Free DNA, Cell-Free Fetal DNA and Soluble Endoglin Levels in Preeclampsia: Predictors of Adverse Fetal Outcome? A Cohort Study.

Published in:

Molecular Diagnosis & Therapy, 2016, v. 20, n. 2, p. 135, doi. 10.1007/s40291-015-0184-x

By:

AbdelHalim, Radwa;
Ramadan, Dalia;
Zeyada, Reham;
Nasr, Ahmed;
Mandour, Iman

Publication type:

Article

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

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

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

Maternal Medication Use, Fetal 3435 C>T Polymorphism of the ABCB1 Gene, and Risk of Isolated Septal Defects in a Han Chinese Population.

Published in:

Pediatric Cardiology, 2014, v. 35, n. 7, p. 1132, doi. 10.1007/s00246-014-0906-6

By:

Wang, Chuan;
Zhou, Kaiyu;
Xie, Liang;
Li, Yifei;
Zhan, Yalan;
Qiao, Lina;
Qin, Chaoyi;
Liu, Ruiqi;
Hua, Yimin

Publication type:

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

Prediction of macrosomia at birth in type-1 and 2 diabetic pregnancies with biomarkers of early placentation.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2011, v. 118, n. 6, p. 748, doi. 10.1111/j.1471-0528.2011.02904.x

By:

Kuc, S.;
Wortelboer, E. J.;
Koster, M. P. H.;
de Valk, H. W.;
Schielen, P. C. J. I.;
Visser, G. H. A.

Publication type:

Article

Prognostic markers of symptomatic congenital human cytomegalovirus infection in fetal blood.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2011, v. 118, n. 4, p. 448, doi. 10.1111/j.1471-0528.2010.02822.x

By:

Fabbri, E.;
Revello, M. G.;
Furione, M.;
Zavattoni, M.;
Lilleri, D.;
Tassis, B.;
Quarenghi, A.;
Rustico, M.;
Nicolini, U.;
Ferrazzi, E.;
Gerna, G.

Publication type:

Article

Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler–Weber–Rendu syndrome): suggested approach for obstetric services.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2008, v. 115, n. 9, p. 1108, doi. 10.1111/j.1471-0528.2008.01786.x

By:

Shovlin, C. L.;
Sodhi, V.;
McCarthy, A.;
Lasjaunias, P.;
Jackson, J. E.;
Sheppard, M. N.

Publication type:

Article