Works matching DE "CHORIONIC villus sampling"

Results: 717

Prevalence of computer vision syndrome in computer users: a systematic review and meta-analysis.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2023, v. 88, n. 10, p. 860, doi. 10.2298/VSP220301024D

By:

Dimitrijević, Vanja;
Todorović, Ivana;
Viduka, Biljana;
Lavrnić, Igor;
Viduka, Dejan

Publication type:

Article

Aneurysmal SAH "A Riddle Wrapped Up in Enigma".

Published in:

2019

By:

Doddamani, Ramesh;
Chandra, Poodipedi;
Doddamani, Ramesh Sharanappa;
Chandra, Poodipedi Sarat

Publication type:

journal article

Embryoscopy and targeted embryo biopsy for the management of early abortion.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 2, p. 655, doi. 10.1007/s10815-024-03356-7

By:

Rouleau, Jean Paul;
Hernández, Jairo;
Costa, Manuela;
Gordon, Tony;
Xanthopoulou, Leoni;
Martín-Vasallo, Pablo;
Naftolin, Frederick;
Palumbo, Angela

Publication type:

Article

Healthy live births achieved from embryos diagnosed as non-mosaic segmental aneuploid.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 12, p. 3379, doi. 10.1007/s10815-024-03282-8

By:

Besser, Andria;
Weidenbaum, Emily;
Buldo-Licciardi, Julia;
McCaffrey, Caroline;
Grifo, James;
Blakemore, Jennifer

Publication type:

Article

Sociocultural imperatives for Singapore to permit preimplantation genetic testing-aneuploidy (PGT-A) despite uncertain results and ongoing controversy.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 6, p. 1377, doi. 10.1007/s10815-023-02836-6

By:

Chin, Alexis Heng Boon;
Sun, Ningyu

Publication type:

Article

Majority of transferred mosaic embryos developed healthy live births revealed by a preclinical study using embryonic morphology assessment and noninvasive PGT-A on cell-free DNA in blastocoel fluid.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 11, p. 2483, doi. 10.1007/s10815-022-02651-5

By:

Cai, Lingbo;
Zeng, Qiao;
Gao, Chao;
Wu, Wei;
Shen, Jiandong;
Wu, Bai-Lin;
Wang, Dao Wu;
Cui, Yugui;
Liu, Jiayin

Publication type:

Article

Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testing.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 8, p. 1959, doi. 10.1007/s10815-021-02104-5

By:

Toft, Christian Liebst Frisk;
Ingerslev, Hans Jakob;
Kesmodel, Ulrik Schiøler;
Hatt, Lotte;
Singh, Ripudaman;
Ravn, Katarina;
Nicolaisen, Bolette Hestbek;
Christensen, Inga Baasch;
Kølvraa, Mathias;
Jeppesen, Line Dahl;
Schelde, Palle;
Vogel, Ida;
Uldbjerg, Niels;
Farlie, Richard;
Sommer, Steffen;
Østergård, Marianne Louise Vang;
Jensen, Ann Nygaard;
Mogensen, Helle;
Kjartansdóttir, Kristín Rós;
Degn, Birte

Publication type:

Article

Letter to Editor.

Published in:

2021

By:

Scriven, Paul N.

Publication type:

Letter

Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 8, p. 2019, doi. 10.1007/s10815-020-01825-3

By:

Okmen, Firat;
Ekici, Huseyin;
Hortu, Ismet;
Imamoglu, Metehan;
Arican, Duygu;
Akın, Haluk;
Sagol, Sermet

Publication type:

Article

Variations in chromosomal aneuploidy rates in IVF blastocysts and early spontaneous abortion chorionic villi.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 3, p. 527, doi. 10.1007/s10815-019-01682-9

By:

Zhang, Xintian;
Wang, Yun;
Zhao, Nan;
Liu, Ping;
Huang, Jin

Publication type:

Article

Embryoscopy and karyotype findings of repeated miscarriages in recurrent pregnancy loss and spontaneous pregnancy loss.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 8, p. 1401, doi. 10.1007/s10815-018-1226-1

By:

Feichtinger, M.;
Reiner, A.;
Hartmann, B.;
Philipp, T.

Publication type:

Article

Zygotic-splitting after in vitro fertilization and prenatal parenthood testing after suspected embryo mix-up – a case report.

Published in:

International Journal of Legal Medicine, 2024, v. 138, n. 5, p. 2057, doi. 10.1007/s00414-024-03245-9

By:

Schulz, Iris;
Schulte, Janine;
Dipl-Med, Dorothea Wand

Publication type:

Article

Diagnostic Performance of Cyclophilin A in Cardiac Surgery-Associated Acute Kidney Injury.

Published in:

Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 108, doi. 10.3390/jcm9010108

By:

Lee, Cheng-Chia;
Chang, Chih-Hsiang;
Cheng, Ya-Lien;
Kuo, George;
Chen, Shao-Wei;
Li, Yi-Jung;
Chen, Yi-Ting;
Tian, Ya-Chung

Publication type:

Article

Metabolomic Investigation of β-Thalassemia in Chorionic Villi Samples.

Published in:

Journal of Clinical Medicine, 2019, v. 8, n. 6, p. 798, doi. 10.3390/jcm8060798

By:

Monni, Giovanni;
Murgia, Federica;
Corda, Valentina;
Peddes, Cristina;
Iuculano, Ambra;
Tronci, Laura;
Balsamo, Antonella;
Atzori, Luigi

Publication type:

Article

Prenatal diagnosis of phenylketonuria: a tertiary center experience.

Published in:

Obstetrică şi Ginecologie, 2024, v. 72, n. 3, p. 132

By:

Beksac, Mehmet Sinan;
Yılmaz, Engin;
Coşkun, Turgay;
Ozguc, Meral;
Cakar, Ayse Nur;
Gurbuz, Berrak Bilginer;
Aydin, Emine;
Buyukeren, Melek;
Orgul, Gokcen;
Ozalp, Imran

Publication type:

Article

Transabdominal Chorionic Villous Sampling in Nigeria: Correlation between Number of Cases and other Variables.

Published in:

West African Journal of Medicine, 2011, v. 30, n. 1, p. 57

By:

Oloyede, O. A. O.

Publication type:

Article

A glimpse of women's health in China.

Published in:

New Zealand Medical Student Journal, 2018, n. 26, p. 41

By:

Wang, Danni

Publication type:

Article

Natural Frequencies Improve Public Understanding of Medical Test Results: An Experimental Study on Various Bayesian Inference Tasks with Multiple Scoring Methods and Non-Bayesian Reasoning Strategies.

Published in:

Medical Decision Making, 2024, v. 44, n. 8, p. 890, doi. 10.1177/0272989X241275191

By:

Kim, Soyun

Publication type:

Article

Pregnancies with positive non-invasive prenatal testing result for sex chromosome abnormalities in a tertiary hospital in Hong Kong.

Published in:

Hong Kong Journal of Gynaecology, Obstetrics & Midwifery, 2022, v. 22, n. 2, p. 87, doi. 10.12809/hkjgom.22.2.07

By:

SO, P. L.;
Lai, S.;
WONG, P. P.;
SIONG, K. H.;
LEUNG, H. K.;
SIN, W. K.;
KAN, Anita S. Y.;
LUK, H. M.;
LO, Ivan F. M.;
YEUNG, K. C. A. U.;
WONG, S. F.

Publication type:

Article

Fetal-onset congenital dyserythropoietic anemia type 1 due to CDAN1 mutations presenting as hydrops fetalis.

Published in:

Pediatric Hematology & Oncology, 2018, v. 35, n. 7/8, p. 447, doi. 10.1080/08880018.2019.1569187

By:

Liu, Sha;
Liu, Ying-Na;
Zhen, Li;
Li, Dong-Zhi

Publication type:

Article

Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations.

Published in:

Genes, 2025, v. 16, n. 4, p. 427, doi. 10.3390/genes16040427

By:

Sirica, Roberto;
Ottaiano, Alessandro;
D'Amore, Luigi;
Ianniello, Monica;
Petrillo, Nadia;
Ruggiero, Raffaella;
Castiello, Rosa;
Mori, Alessio;
Evangelista, Eloisa;
De Falco, Luigia;
Santorsola, Mariachiara;
Misasi, Michele;
Savarese, Giovanni;
Fico, Antonio

Publication type:

Article

Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023.

Published in:

2023

By:

Godler, David E.;
Brown, William T.

Publication type:

Editorial

Prenatal Detection of Trisomy 2: Considerations for Genetic Counseling and Testing.

Published in:

Genes, 2023, v. 14, n. 4, p. 913, doi. 10.3390/genes14040913

By:

Talantova, Olga E.;
Koltsova, Alla S.;
Tikhonov, Andrei V.;
Pendina, Anna A.;
Malysheva, Olga V.;
Tarasenko, Olga A.;
Vashukova, Elena S.;
Shabanova, Elena S.;
Golubeva, Arina V.;
Chiryaeva, Olga G.;
Glotov, Andrey S.;
Bespalova, Olesya N.;
Efimova, Olga A.

Publication type:

Article

Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies.

Published in:

Genes, 2022, v. 13, n. 12, p. 2389, doi. 10.3390/genes13122389

By:

Basaran, Seher;
Has, Recep;
Kalelioglu, Ibrahim Halil;
Sarac Sivrikoz, Tugba;
Karaman, Birsen;
Kirgiz, Melike;
Dehgan, Tahir;
Kalayci, Tugba;
Ozsait Selcuk, Bilge;
Miny, Peter;
Yuksel, Atil

Publication type:

Article

Whole-Chromosome Karyotyping of Fetal Nucleated Red Blood Cells Using the Ion Proton Sequencing Platform.

Published in:

Genes, 2022, v. 13, n. 12, p. 2257, doi. 10.3390/genes13122257

By:

Barrett, Angela N.;
Huang, Zhouwei;
Aung, Sarah;
Ho, Sherry S. Y.;
Roslan, Nur Syazana;
Mahyuddin, Aniza P.;
Biswas, Arijit;
Choolani, Mahesh

Publication type:

Article

Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX.

Published in:

Genes, 2021, v. 13, n. 6, p. 798, doi. 10.3390/genes12060798

By:

Pandelache, Alison;
Francis, David;
Oertel, Ralph;
Dickson, Rebecca;
Sachdev, Rani;
Ling, Ling;
Gamage, Dinusha;
Godler, David E.

Publication type:

Article

Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular Dystrophy.

Published in:

Journal of Pregnancy, 2018, p. 1, doi. 10.1155/2018/9718316

By:

Beksac, Mehmet Sinan;
Tanacan, Atakan;
Aydin Hakli, Duygu;
Orgul, Gokcen;
Soyak, Burcu;
Balci Hayta, Burcu;
Dincer, Pervin;
Topaloğlu, Haluk

Publication type:

Article

DNA methylation abnormalities induced by advanced maternal age in villi prime a high-risk state for spontaneous abortion.

Published in:

Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01432-w

By:

Qin, Meng;
Chen, Wei;
Hua, Lingyue;
Meng, Yan;
Wang, Jing;
Li, Hanna;
Yang, Rui;
Yan, Liying;
Qiao, Jie

Publication type:

Article

Non invasive prenatal diagnosis of β- Thalassemia, A narrative review study.

Published in:

Bangladesh Journal of Medical Science, 2017, v. 16, n. 2, p. 196, doi. 10.3329/bjms.v16i2.25305

By:

Zafari, M.;
Kowsaryan, M.;
Gill, P.;
Banihashemi, A.

Publication type:

Article

Magnitude and determinants of computer vision syndrome among college students at a Saudi University.

Published in:

Middle East African Journal of Ophthalmology, 2021, v. 28, n. 4, p. 252, doi. 10.4103/meajo.meajo_272_21

By:

AlDarrab, Abdulrahman;
Khojah, Abdulaziz;
Al-Ghazwi, Mohammed;
Al-Haqbani, Yazeed;
Al-Qahtani, Naif;
Al-Ajmi, Mohammed;
Alenezi, Saad;
Almasoud, Mohammmed;
Al-Yahya, Abdulaziz

Publication type:

Article

Confined placental mosaicism of Duchenne muscular dystrophy: a case report.

Published in:

Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00520-3

By:

Winerdal, Max;
Westenius, Eini;
Granfors, Michaela;
Pettersson, Maria;
Iwarsson, Erik

Publication type:

Article

Submicroscopic chromosomal imbalances contribute to early abortion.

Published in:

Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0386-0

By:

Li, Haibo;
Liu, Minjuan;
Xie, Min;
Zhang, Qin;
Xiang, Jingjing;
Duan, Chengying;
Ding, Yang;
Liu, Yinghua;
Mao, Jun;
Wang, Ting;
Li, Hong

Publication type:

Article

Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology.

Published in:

Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-015-0210-z

By:

Jiandong Shen;
Wei Wu;
Chao Gao;
Humphrey Ochin;
Dianyun Qu;
Jiazi Xie;
Li Gao;
Yadong Zhou;
Yugui Cui;
Jiayin Liu

Publication type:

Article

Comparison between open and closed systems for vitrification of individual sperm: assessing morphometric measurements and chromatin integrity.

Published in:

Middle East Fertility Society Journal, 2024, v. 29, n. 1, p. 1, doi. 10.1186/s43043-024-00188-4

By:

Khalili, Mohammad Ali;
Vatanparast, Mahboubeh;
Mangoli, Esmat;
Ghasmi-Esmaeilabad, Saeed;
Moshrefi, Mojgan;
Hosseini, Akram

Publication type:

Article

Prenatal quantitation of number of X-chromosomes by slot blot hybridization and autoradiography.

Published in:

1993

By:

Chan, F.Y.;
Chan, V.;
Chan, T.K.

Publication type:

journal article

The SafeBirth Clinic.

Published in:

INFORMS Transactions on Education, 2021, v. 22, n. 1, p. 148, doi. 10.1287/ited.2019.0241cs

By:

Dawande, Milind;
Huh, Woonghee Tim;
Janakiraman, Ganesh;
Nagarajan, Mahesh;
Bo, Yang

Publication type:

Article

Detection and distribution of culturable Human Enteroviruses through environmental surveillance in Milan, Italy.

Published in:

Journal of Applied Microbiology, 2013, v. 115, n. 5, p. 1231, doi. 10.1111/jam.12321

By:

Pellegrinelli, L.;
Binda, S.;
Chiaramonte, I.;
Primache, V.;
Fiore, L.;
Battistone, A.;
Fiore, S.;
Gambino, M.;
Bubba, L.;
Barbi, M.

Publication type:

Article

Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.

Published in:

Nature Medicine, 2007, v. 13, n. 2, p. 218, doi. 10.1038/nm1530

By:

Lo, Y. M. Dennis;
Tsui, Nancy B. Y.;
Chiu, Rossa W. K.;
Lau, Tze K.;
Leung, Tse N.;
Heung, Macy M. S.;
Gerovassili, Ageliki;
Jin, Yongjie;
Nicolaides, Kypros H.;
Cantor, Charles R.;
Ding, Chunming

Publication type:

Article

Amniocentesis test uptake for congenital defects: Decision of pregnant women in Vietnam.

Published in:

Health Care for Women International, 2018, v. 39, n. 4, p. 493, doi. 10.1080/07399332.2018.1424168

By:

Canh Chuong, Nguyen;
Minh Duc, Duong;
Anh, Nguyen Duy;
Thi Vui, Le;
Pham Sy Cuong, Le;
Thi Thuy Duong, Doan;
Thi Thu Ha, Bui

Publication type:

Article

Multidisciplinary Management of Pregnancy in Patients With Osteogenesis Imperfecta Type 3.

Published in:

Permanente Journal, 2024, v. 28, n. 3, p. 190, doi. 10.7812/TPP/23.168

By:

Partani, Ekta;
Stephenson, Megan L.

Publication type:

Article

Treatment of obstructive sleep apnea in high risk pregnancy: a multicenter randomized controlled trial.

Published in:

Respiratory Research, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12931-023-02445-y

By:

Tantrakul, Visasiri;
Ingsathit, Atiporn;
Liamsombut, Somprasong;
Rattanasiri, Sasivimol;
Kittivoravitkul, Prapun;
Imsom-Somboon, Nutthaphon;
Lertpongpiroon, Siwaporn;
Jantarasaengaram, Surasak;
Somchit, Werapath;
Suwansathit, Worakot;
Pengjam, Janejira;
Siriyotha, Sukanya;
Panburana, Panyu;
Guilleminault, Christian;
Preutthipan, Aroonwan;
Attia, John;
Thakkinstian, Ammarin

Publication type:

Article

'It made you think twice' - an interview study of women's perception of a web-based decision aid concerning screening and diagnostic testing for fetal anomalies.

Published in:

2016

By:

Åhman, Annika;
Sarkadi, Anna;
Lindgren, Peter;
Rubertsson, Christine

Publication type:

journal article

Congenital Ichthyosis: Current Approaches to Prenatal Diagnoses.

Published in:

Fetal & Pediatric Pathology, 2024, v. 43, n. 2, p. 157, doi. 10.1080/15513815.2023.2301468

By:

Mahmood Alsabbagh, Manahel

Publication type:

Article

Complementary Approaches in Fetal Genetic Diagnosis: Decision-Making Process and Alternative Choices for Clinicians in a Secondary Health Care Institution.

Published in:

Fetal & Pediatric Pathology, 2022, v. 41, n. 6, p. 944, doi. 10.1080/15513815.2021.2022818

By:

Bolat, Hilmi;
Çelebi, Hamide Betül Gerik;
Karahanoğlu, Ertuğrul

Publication type:

Article

Histological Evaluation of Products of Conception, Who Benefits from It?

Published in:

Fetal & Pediatric Pathology, 2023, v. 42, n. 1, p. 30, doi. 10.1080/15513815.2022.2053916

By:

Soltanghoraee, Haleh;
Mohazzab, Arash;
Soltani, Azadeh;
Ansaripour, Soheila;
Tavakoli, Maryam;
Rafati, Maryam;
Zarnani, Amir Hassan;
Ghaffari, Saeed Reza

Publication type:

Article

Fetal Genetic Diagnosis by Chorionic Villus Sampling: Evaluation of the Five-Year Experience from a Single Center.

Published in:

Fetal & Pediatric Pathology, 2021, v. 40, n. 4, p. 281, doi. 10.1080/15513815.2019.1707919

By:

Öztürk, Filiz Halici;
Öcal, Fatma Doga;
Erol, Seyit Ahmet;
Yakut, Kadriye;
Öztürk, Merve;
Oguz, Yüksel;
Çakar, Esra Sükran;
Celen, Sevki;
Çaglar, Ali Turhan

Publication type:

Article

Trisomy 18 in a First-Trimester Fetus with Thoraco-Abdominal Ectopia Cordis.

Published in:

Fetal & Pediatric Pathology, 2020, v. 39, n. 1, p. 78, doi. 10.1080/15513815.2019.1629132

By:

Diaz-Serani, Ricardo;
Sepulveda, Waldo

Publication type:

Article

Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy.

Published in:

Fetal & Pediatric Pathology, 2018, v. 37, n. 6, p. 418, doi. 10.1080/15513815.2018.1520944

By:

Fadiloglu, Erdem;
Ozten, Gonca;
Unal, Canan;
Talim, Beril;
Topaloglu, Haluk;
Beksac, Mehmet Sinan

Publication type:

Article

Prenatally Diagnosed Hemophilia in a Newborn: a Case Report.

Published in:

Fetal & Pediatric Pathology, 2015, v. 34, n. 4, p. 248, doi. 10.3109/15513815.2015.1051250

By:

Jovandaric, Miljana Zivojin;
Jesic, Milos M.

Publication type:

Article

Detection of Clonal Aberrations by Cytogenetic Analysis after Different Culture Methods and by FISH in 129 Patients with Chronic Lymphocytic Leukemia.

Published in:

Cytogenetic & Genome Research, 2015, v. 144, n. 3, p. 163, doi. 10.1159/000369543

By:

Jenderny, Jutta;
Goldmann, Claudia;
Thede, Rebekka;
Ebrecht, Monika;
Korioth, Frank

Publication type:

Article