Amniocentesis and chorionic villus sampling for prenatal diagnosis - Wikidata - awgldk - TriplyDB

Amniocentesis and chorionic villus sampling for prenatal diagnosis

Amniocentesis and chorionic villus sampling for prenatal diagnosis

http://www.wikidata.org/entity/Q24247990

about

Second trimester serum tests for Down's Syndrome screening Prenatal education for congenital toxoplasmosis Urine tests for Down's syndrome screening First trimester serum tests for Down's syndrome screening Antenatal screening for Down's syndrome: generic protocol Different communication strategies for disclosing results of diagnostic prenatal testing Non-invasive prenatal diagnosis of fetal trisomy 21 using cell-free fetal DNA in maternal blood Placental mesenchymal stromal cells rescue ambulation in ovine myelomeningocele.Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome.Qualifying choice: ethical reflection on the scope of prenatal screening.The first 3,000 Non-Invasive Prenatal Tests (NIPT) with the Harmony test in Belgium and the Netherlands.Diagnosis of and screening for cytomegalovirus infection in pregnant women.Comparison of complications of chorionic villus sampling and amniocentesis Systematic review of methods used in meta-analyses where a primary outcome is an adverse or unintended event Towards standardisation of cell-free DNA measurement in plasma: controls for extraction efficiency, fragment size bias and quantification Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.A framework for analyzing sex-selective abortion: the example of changing sex ratios in Southern Caucasus.Introducing the non-invasive prenatal test for trisomy 21 in Belgium: a cost-consequences analysis Epigenetic approaches for the detection of fetal DNA in maternal plasma.Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities.The Maternal Serological Response to Intrauterine Ureaplasma sp. Infection and Prediction of Risk of Pre-Term Birth.Biology of infantile hemangioma First trimester diagnosis and screening for fetal aneuploidy.Screening for fetal aneuploidy and neural tube defects Disease specific characteristics of fetal epigenetic markers for non-invasive prenatal testing of trisomy 21 Developmental stage determines efficiency of gene transfer to muscle satellite cells by in utero delivery of adeno-associated virus vector serotype 2/9 Prenatal screening of cytogenetic anomalies - a Western Indian experience Regulatory and ethical issues for phase I in utero gene transfer studies.Impact of Cell-Free Fetal DNA Screening on Patients' Choice of Invasive Procedures after a Positive California Prenatal Screen Result.Explore the dynamic alternation of gene PLAC4 mRNA expression levels in maternal plasma in second trimester for nonivasive detection of trisomy 21 In utero transplantation: baby steps towards an effective therapy.Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases Antenatal diagnosis of fetal genotype determines if maternal hyperglycemia due to a glucokinase mutation requires treatment First trimester ultrasound tests alone or in combination with first trimester serum tests for Down's syndrome screening.First and second trimester serum tests with and without first trimester ultrasound tests for Down's syndrome screening.Cell free fetal DNA testing in maternal blood of Romanian pregnant women Percutaneous in utero thoracoamniotic shunt creation for fetal thoracic abnormalities leading to nonimmune hydrops.A four-year retrospective study of amniocentesis: one centre experience.Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study.

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

http://www.wikidata.org/entity/Q24247990

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2003 nî lūn-bûn

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2003 թվականին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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Cochrane Database of Systematic Reviews

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Amniocentesis and chorionic villus sampling for prenatal diagnosis

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K Sundberg

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P2860

Instruments for chorionic villus sampling for prenatal diagnosis

Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)

Randomised controlled trial of genetic amniocentesis in 4606 low-risk women.

Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling.

Club foot, an adverse outcome of early amniocentesis: disruption or deformation? CEMAT. Canadian Early and Mid-Trimester Amniocentesis Trial.

Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review.

Randomised comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling.

Does light pressure effleurage reduce pain and anxiety associated with genetic amniocentesis? A randomized clinical trial.

A controlled trial of puncture sites for amniocentesis.

Experience with early amniocentesis.

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