听力与言语-语言病理学

行为科学

医学伦理学

你正在浏览Birth Defects Research期刊下所有文献
  • Maternal Medicaid Recipient Status and Congenital Malformations among New York State Live Births in 2010.

    abstract:BACKGROUND:Congenital malformations are a leading cause of infant mortality in the United States, and risk for some congenital malformations varies by socioeconomic status (SES). Medicaid provides health insurance for people with low income, and covers approximately half of all live births in the United States. Income ...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1107

    authors: Richardson SD,Josberger RE

    更新日期:2017-11-01 00:00:00

  • Association Study of Transforming Growth Factor Alpha TaqI Polymorphism and the Risk of Cleft Lip and/or Palate in an Iranian Population.

    abstract:BACKGROUND:The aim of this study is to evaluate the association of TGFA TaqI polymorphism with nonsyndromic cleft lip and/or palate (NSCLP) in an Iranian population. METHODS:In this case-control study, 113 children with NSCLP and 209 controls were included. Genotyping of the TaqI polymorphism was performed by polymera...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1125

    authors: Bagheri F,Ebadifar A,Khorram Khorshid HR,Kamali K

    更新日期:2017-10-16 00:00:00

  • Congenital unilateral renal agenesis: Prevalence, prenatal diagnosis, associated anomalies. Data from two birth-defect registries.

    abstract:BACKGROUND:The different mechanisms leading to a solitary kidney should be differentiated because the long-term outcome might be different. The fetal period is the best moment to make a true diagnosis of congenital unilateral renal agenesis (URA). The objective was to determine the prevalence of URA at birth. The secon...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1065

    authors: Laurichesse Delmas H,Kohler M,Doray B,Lémery D,Francannet C,Quistrebert J,Marie C,Perthus I

    更新日期:2017-09-01 00:00:00

  • Ambient and Dosed Exposure to Quaternary Ammonium Disinfectants Causes Neural Tube Defects in Rodents.

    abstract:BACKGROUND:Quaternary ammonium compounds are a large class of chemicals used for their antimicrobial and antistatic properties. Two common quaternary ammonium compounds, alkyldimethylbenzyl ammonium chloride (ADBAC) and didecyldimethyl ammonium chloride (DDAC), are combined in common cleaners and disinfectants. Introdu...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1064

    authors: Hrubec TC,Melin VE,Shea CS,Ferguson EE,Garofola C,Repine CM,Chapman TW,Patel HR,Razvi RM,Sugrue JE,Potineni H,Magnin-Bissel G,Hunt PA

    更新日期:2017-08-15 00:00:00

  • Animal Embryotoxicity Studies of Key Non-Artemisinin Antimalarials and Use in Women in the First Trimester.

    abstract::The World Health Organization currently recommends quinine+clindamycin for use against malaria in the first trimester. This may soon change to recommending artemisinin-based combination therapies (standard duration of dosing = 3 days). The non-artemisinin partner drugs include amodiaquine, lumefantrine, mefloquine, pi...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdr2.1035

    authors: Clark RL

    更新日期:2017-08-15 00:00:00

  • Use of Psychotropic Medications in Breastfeeding Women.

    abstract:BACKGROUND:Breastfeeding women who are prescribed with psychotropic medications on a regular basis are often concerned, regarding the possible implications of such treatment on the breastfed infant. A mother's well-being has a direct influence on the well-being of the baby. However, the notorious reputation of psychotr...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdr2.1077

    authors: Kronenfeld N,Berlin M,Shaniv D,Berkovitch M

    更新日期:2017-07-17 00:00:00

  • Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

    abstract:BACKGROUND:The acronym VATER/VACTERL refers to the rare nonrandom association of the following component features (CF): vertebral defects (V), anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia, renal malformations (R), and limb defects (L). Patients presentin...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1042

    authors: Zhang R,Marsch F,Kause F,Degenhardt F,Schmiedeke E,Märzheuser S,Hoppe B,Bachour H,Boemers TM,Schäfer M,Spychalski N,Neser J,Leonhardt J,Kosch F,Ure B,Gómez B,Lacher M,Deffaa OJ,Palta M,Wittekindt B,Kleine K,Schm

    更新日期:2017-07-17 00:00:00

  • Phenotyping cardiac and structural birth defects in fetal and newborn mice.

    abstract::Mouse models are invaluable for investigating the developmental etiology and molecular pathogenesis of structural birth defects. While this has been deployed for studying a wide spectrum of birth defects, mice are particularly valuable for modeling congenital heart disease, given they have the same four-chamber cardia...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdr2.1048

    authors: Liu X,Kim AJ,Reynolds W,Wu Y,Lo CW

    更新日期:2017-06-01 00:00:00

  • Diverse application of MRI for mouse phenotyping.

    abstract::Small animal models, particularly mouse models, of human diseases are becoming an indispensable tool for biomedical research. Studies in animal models have provided important insights into the etiology of diseases and accelerated the development of therapeutic strategies. Detailed phenotypic characterization is essent...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdr2.1051

    authors: Wu YL,Lo CW

    更新日期:2017-06-01 00:00:00

  • Screening, genetics, risk factors, and treatment of neonatal cataracts.

    abstract::Neonatal cataracts remain the most common cause of visual loss in children worldwide and have diverse, often unknown, etiologies. This review summarizes current knowledge about the detection, treatment, genetics, risk factors, and molecular mechanisms of congenital cataracts. We emphasize significant progress and topi...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdr2.1050

    authors: Li J,Xia CH,Wang E,Yao K,Gong X

    更新日期:2017-06-01 00:00:00

  • High Ratios of C20:4n-6/C20:5n-3 and Thromboxane B2 /6-Keto-Prostaglandin F1α in Placenta Are Potential Risk Contributors for Neural Tube Defects: A Case-Control Study in Shanxi Province, China.

    abstract:BACKGROUND:Neural tube defects (NTDs) are severe congenital malformations. Folate supplementation can reduce the risk, but cannot prevent all NTDs, suggesting other reasons for folate-resistant NTDs. The present study assesses placental fatty acid composition, eicosanoids, and cytokines as risk factors for NTDs in a Ch...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1003

    authors: Li K,Zhang X,Pei L,Chen G,Liu J,Wahlqvist ML,Zheng X,Li D

    更新日期:2017-05-01 00:00:00

  • Gestational and Lactational Exposure to an Environmentally-Relevant Mixture of Brominated Flame Retardants: Effects on Neurodevelopment and Metabolism.

    abstract:BACKGROUND:Developmental exposure to brominated flame retardants (BFRs), including polybrominated diphenyl ethers (PBDEs) and hexabromocyclododecane (HBCDD), has been associated with impaired neurodevelopment and some symptoms of metabolic syndrome. However, there are inconsistencies in studies reporting neurodevelopme...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdr2.1021

    authors: Tung EWY,Kawata A,Rigden M,Bowers WJ,Caldwell D,Holloway AC,Robaire B,Hales BF,Wade MG

    更新日期:2017-04-17 00:00:00

  • Cytomegalovirus infection in pregnancy.

    abstract::Cytomegalovirus (CMV) is a DNA herpesvirus that is common worldwide. The two known main sources of primary CMV infection during pregnancy are through sexual activity and contact with young children. Primary infection occurs in approximately 1 to 4% of pregnancies, and is mostly asymptomatic in immunocompetent adults. ...

    journal_title:Birth defects research

    pub_type: 杂志文章,评审

    doi:10.1002/bdra.23601

    authors: Davis NL,King CC,Kourtis AP

    更新日期:2017-03-15 00:00:00

  • White paper on the study of birth defects.

    abstract::Birth defects are the leading cause of infant death in the United States and among the top causes of pediatric death and hospitalization. Despite the devastating impact of birth defects, we understand little of their etiology impeding progress towards treatment and prevention. Moreover, while surgical interventions ha...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdra.23590

    authors: Khokha MK,Mitchell LE,Wallingford JB

    更新日期:2017-01-30 00:00:00

  • Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.

    abstract:BACKGROUND:Recent advances in genomics methodologies, in particular the availability of next-generation sequencing approaches have made it possible to identify risk loci throughout the genome, in particular the exome. In the current study, we present findings from an exome study conducted in five affected individuals o...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdra.23596

    authors: Liu H,Busch T,Eliason S,Anand D,Bullard S,Gowans LJJ,Nidey N,Petrin A,Augustine-Akpan EA,Saadi I,Dunnwald M,Lachke SA,Zhu Y,Adeyemo A,Amendt B,Roscioli T,Cornell R,Murray J,Butali A

    更新日期:2017-01-20 00:00:00

  • Rare copy number variants in a population-based investigation of hypoplastic right heart syndrome.

    abstract:BACKGROUND:Hypoplastic right heart syndrome (HRHS) is a rare congenital defect characterized by underdevelopment of the right heart structures commonly accompanied by an atrial septal defect. Familial HRHS reports suggest genetic factor involvement. We examined the role of copy number variants (CNVs) in HRHS. METHODS:...

    journal_title:Birth defects research

    pub_type: 杂志文章

    doi:10.1002/bdra.23586

    authors: Dimopoulos A,Sicko RJ,Kay DM,Rigler SL,Druschel CM,Caggana M,Browne ML,Fan R,Romitti PA,Brody LC,Mills JL

    更新日期:2017-01-20 00:00:00

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