Works matching DE "GENETIC disorders in pregnancy"

Results: 86

Obstetric outcomes of IVF trichorionic triamniotic triplets which are spontaneously or electively reduced to twins.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 12, p. 1217, doi. 10.1007/s10815-011-9651-4

By:

Ata, B.;
Rasillo, L.;
Sukhdeo, S.;
Son, W.;
Tan, S.;
Dahan, M.

Publication type:

Article

Early pregnancy loss rates were different among singleton gestations conceived by ICSI using GnRH agonist and antagonist.

Published in:

Journal of Assisted Reproduction & Genetics, 2009, v. 26, n. 4, p. 227, doi. 10.1007/s10815-009-9303-0

By:

Bahceci, Mustafa;
Ulug, Ulun;
Sismanoglu, Alper;
Tosun, Suleyman;
Cengiz, Bora

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

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

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

The presence of multiple gestational sacs confers a higher live birth rate in women with infertility who achieve a positive pregnancy test after fresh and frozen embryo transfer: a retrospective local cohort.

Published in:

Reproductive Biology & Endocrinology, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1477-7827-12-104

By:

Balassiano, Erika;
Malik, Shaveta;
Vaid, Praful;
Knochenhauer, Eric S.;
Traub, Michael L.

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

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

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 proportions of Down's syndrome pregnancies detected prenatally in England and Wales from 1989 to 2004.

Published in:

Journal of Medical Screening, 2006, v. 13, n. 4, p. 163, doi. 10.1177/096914130601300401

By:

Morris, J. K.;
Alberman, E.;
Mutton, D.

Publication type:

Article

Noninvasive Prenatal Diagnosis of Fetal Trisomy 21 by Allelic Ratio Analysis Using Targeted Massively Parallel Sequencing of Maternal Plasma DNA.

Published in:

PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0038154

By:

Liao, Gary J. W.;
Chan, K. C. Allen;
Jiang, Peiyong;
Hao Sun;
Leung, Tak Y.;
Chiu, Rossa W. K.;
Lo, Y. M. Dennis

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

Umbilicus as a fitness signal in humans.

Published in:

2009

By:

Sinkkonen, Aki

Publication type:

Essay

Twin Pregnancy With Partial Hydatidiform Mole and Coexistent Fetus.

Published in:

Archives of Pathology & Laboratory Medicine, 2004, v. 128, n. 11, p. 1305, doi. 10.5858/2004-128-1305-tpwphm

By:

Chu, Wenjiang;
Chapman, Julia;
Persons, Diane L.;
Fan, Fang

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

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

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

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

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

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

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 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

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

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

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

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

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

Pre- and periconceptional primary cytomegalovirus infection: risk of vertical transmission and congenital disease.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2005, v. 112, n. 2, p. 166, doi. 10.1111/j.1471-0528.2004.00328.x

By:

Daiminger, A.;
Bäder, U.;
Enders, G.

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

Re1B/p52 NF-κB Complexes Rescue an Early Delay in Mammary Gland Development in Transgenic Mice with Targeted Superrepressor IκB-α Expression and Promote Carcinogenesis of the Mammary Gland.

Published in:

Molecular & Cellular Biology, 2005, v. 25, n. 22, p. 10136, doi. 10.1128/MCB.25.22.10136-10147.2005

By:

Demicco, Elizabeth G.;
Kavanagh, Kathryn T.;
Romieu-Mourez, Raphaëlle;
Xiaobo Wang;
Shin, Sangmin R.;
Landesman-Bollag, Esther;
Seldin, David C.;
Sonenshein, Gail E.

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

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

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

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

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