Works matching Trisomy 18 syndrome

Results: 562

Population-Based Analysis of Secular Trends in Age at Death in Trisomy 18 Syndrome in Japan from 1975 to 2016.

Published in:

Neonatology (16617800), 2021, v. 118, n. 1, p. 47, doi. 10.1159/000512922

By:

Suto, Maiko;
Isayama, Tetsuya;
Morisaki, Naho

Publication type:

Article

Anesthesia for children with complete trisomy 18 (Edwards syndrome): A cohort review of 84 anesthesia encounters in nine patients.

Published in:

Pediatric Anesthesia, 2021, v. 31, n. 4, p. 419, doi. 10.1111/pan.14131

By:

Birmingham, Erin E.;
Stucke, Astrid G.;
Diaz, Christina D.;
Veyckemans, Francis

Publication type:

Article

Reply to the Letter to the Editor "Underestimation of Trisomy 18 and 13 Syndromes in Vital Statistics from Inadequate Death Certificates".

Published in:

Neonatology (16617800), 2022, v. 119, n. 1, p. 135, doi. 10.1159/000520243

By:

Suto, Maiko;
Isayama, Tetsuya;
Takehara, Kenji;
Morisaki, Naho

Publication type:

Article

VACTERL Association with Meningomyelocele Combined with Trisomy 18 Syndrome.

Published in:

Neonatal Medicine, 2014, v. 21, n. 1, p. 74, doi. 10.5385/nm.2014.21.1.74

By:

Yu Kyong Kim;
Ji Hoon Lee;
Ga Won Jeon;
Jong Beom Sin

Publication type:

Article

Underestimation of Trisomy 18 and 13 Syndromes in Vital Statistics from Inadequate Death Certificates.

Published in:

2022

By:

Takashima, Kohei;
Hitosugi, Masahito

Publication type:

Letter

VACTERL associated with a rare limb anomaly combined with edward (trisomy 18) syndrome.

Published in:

Journal of Indian Association of Pediatric Surgeons, 2021, v. 26, n. 3, p. 206, doi. 10.4103/jiaps.JIAPS_237_20

By:

Hasan, Zaheer;
Thakur, Vinit;
Chaubey, Digamber;
Rahul, Sandip;
Kumar, Sujit

Publication type:

Article

Sequential integrated antenatal screening for Down’s syndrome, trisomy 18 and trisomy 13.

Published in:

Journal of Medical Screening, 2016, v. 23, n. 3, p. 116, doi. 10.1177/0969141315608895

By:

Bestwick, Jonathan P.;
Wald, Nicholas J.

Publication type:

Article

Antenatal screening for Down’s syndrome, trisomy 18, and trisomy 13: Reporting a single screening result for all three.

Published in:

Journal of Medical Screening, 2015, v. 22, n. 2, p. 100, doi. 10.1177/0969141315575545

By:

Bestwick, Jonathan P;
Wald, Nicholas J

Publication type:

Article

Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome.

Published in:

Hormone Research in Paediatrics, 2017, v. 87, n. 2, p. 130, doi. 10.1159/000448172

By:

MacMahon, Jayne M.;
O'Sullivan, Maureen J.;
McDermott, Michael;
Quinn, Feargal;
Morris, Thomas;
Green, andrew J.;
Betts, David R.;
O'Connell, Susan M.

Publication type:

Article

Aberrant “Barbed-Wire” Nuclear Projections of Neutrophils in Trisomy 18 (Edwards Syndrome).

Published in:

2015

By:

Kahwash, Basil M.;
Nowacki, Nicholas B.;
Kahwash, Samir B.

Publication type:

Case Study

Aberrant “Barbed-Wire” Nuclear Projections of Neutrophils in Trisomy 18 (Edwards Syndrome).

Published in:

Case Reports in Hematology, 2015, p. 1, doi. 10.1155/2015/163857

By:

Kahwash, Basil M.;
Nowacki, Nicholas B.;
Kahwash, Samir B.

Publication type:

Article

Letální syndromy v pediatrii – tři příběhy trizomie 18.

Published in:

Pediatrie pro Praxi, 2023, v. 24, n. 2, p. 111, doi. 10.36290/ped.2023.033

By:

Ducháčová, Michaela;
Pavlíček, Jan;
Pavlíčková, Eva;
Nowaková, Markéta;
Trávníček, Bořek;
Kuzníková, Iva;
Broďáková, Tereza

Publication type:

Article

Two-Dimensional Differential Gel Electrophoresis to Identify Protein Biomarkers in Amniotic Fluid of Edwards Syndrome (Trisomy 18) Pregnancies.

Published in:

PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0145908

By:

Hsu, Te-Yao;
Lin, Hao;
Hung, Hsuan-Ning;
Yang, Kuender D.;
Ou, Chia-Yu;
Tsai, Ching-Chang;
Cheng, Hsin-Hsin;
Chung, Su-Hai;
Cheng, Bi-Hua;
Wong, Yi-Hsun;
Chou, An Kuo;
Hsiao, Chang-Chun

Publication type:

Article

Antenatal detection of Edwards (Trisomy 18) and Patau (Trisomy 13) syndrome: England and Wales 2005-2012.

Published in:

Journal of Medical Screening, 2014, v. 21, n. 3, p. 113, doi. 10.1177/0969141314543128

By:

Springett, Anna L;
Morris, Joan K

Publication type:

Article

Single-cell chromatin accessibility landscape of human umbilical cord blood in trisomy 18 syndrome.

Published in:

Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00338-z

By:

Qiu, Xiaofen;
Yu, Haiyan;
Wu, Hongwei;
Hu, Zhiyang;
Zhou, Jun;
Lin, Hua;
Xue, Wen;
Cai, Wanxia;
Chen, Jiejing;
Yan, Qiang;
Dai, Weier;
Yang, Ming;
Tang, Donge;
Dai, Yong

Publication type:

Article

Trizomi 18 Sendromu: Olgu Sunumu.

Published in:

2012

By:

Karaman, Ali;
Kahveci, Hasan;
Laloğlu, Fuat

Publication type:

Case Study

Survival of children with trisomy 18 associated with the presence of congenital heart disease and intervention in the Republic of Korea.

Published in:

BMC Pediatrics, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12887-023-04056-4

By:

Song, In Gyu;
Shin, Seung Han;
Cho, Yoon-Min;
Lim, Youna

Publication type:

Article

Patau and Edwards Syndromes in a University Hospital: beyond palliative care.

Published in:

Revista Paulista de Pediatria, 2024, v. 42, p. 1, doi. 10.1590/1984-0462/2024/42/2023053

By:

Marçola, Ligia;
Zoboli, Ivete;
Verardo Polastrini, Rita Tiziana;
de Macedo Barbosa, Silvia Maria;
Cícero Falcão, Mário;
de Vicenzi Gaiolla, Paula

Publication type:

Article

Future Perspectives in Oxidative Stress in Trisomy 13 and 18 Evaluation.

Published in:

Journal of Clinical Medicine, 2022, v. 11, n. 7, p. 1787, doi. 10.3390/jcm11071787

By:

Buczyńska, Angelika;
Sidorkiewicz, Iwona;
Hameed, Ahsan;
Krętowski, Adam Jacek;
Zbucka-Krętowska, Monika

Publication type:

Article

Palijativno kardiokirurško liječenje u djeteta s Edwardsovim sindromom.

Published in:

Lijecnicki Vjesnik, 2022, v. 144, p. 36, doi. 10.26800/LV-144-supl6-PS09

By:

Gržan, Dina;
Kulaš, Marjan;
Jukić, Lea;
Frković, Sanda Huljev

Publication type:

Article

CONDUCTA MÉDICA FRENTE AL DIAGNÓSTICO PRENATAL DE TRISOMÍA 18: ¿SE APROXIMA UN CAMBIO DE PARADIGMA?

Published in:

Persona y Bioética, 2022, v. 26, n. 2, p. 1, doi. 10.5294/PEBI.2022.26.2.6

By:

Grimaux, Guadalupe;
Páez, Gustavo

Publication type:

Article

Non‐surgical intervention for open myelomeningocele in an infant with trisomy 18.

Published in:

Pediatrics International, 2020, v. 62, n. 4, p. 496, doi. 10.1111/ped.14094

By:

Shitara, Yoshihiko;
Oida, Noriyasu;
Kondo, Utako;
Kushima, Reiko;
Omori, Isaku

Publication type:

Article

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.

Published in:

Neuropathology, 2014, v. 34, n. 3, p. 219, doi. 10.1111/neup.12081

By:

Miyata, Hajime;
Miyata, Mio;
Ohama, Eisaku

Publication type:

Article

First-trimester screening for trisomies 18 and 13, triploidy and Turner syndrome by detailed early anomaly scan.

Published in:

2016

By:

Wagner, P.;
Sonek, J.;
Hoopmann, M.;
Abele, H.;
Kagan, K. O.

Publication type:

journal article

Facial markers in second- and third-trimester fetuses with trisomy 18 or 13, triploidy or Turner syndrome.

Published in:

Ultrasound in Obstetrics & Gynecology, 2015, v. 46, n. 1, p. 60, doi. 10.1002/uog.14655

By:

Kagan, K. O.;
Sonek, J.;
Berg, X.;
Berg, C.;
Mallmann, M.;
Abele, H.;
Hoopmann, M.;
Geipel, A.

Publication type:

Article

Tricuspid regurgitation in screening for trisomies 21, 18 and 13 and Turner syndrome at 11+0 to 13+6 weeks of gestation.

Published in:

2009

By:

Kagan KO;
Valencia C;
Livanos P;
Wright D;
Nicolaides KH;
Kagan, K O;
Valencia, C;
Livanos, P;
Wright, D;
Nicolaides, K H

Publication type:

journal article

Follow up and evaluation of the Victorian first-trimester combined screening programme for Down syndrome and trisomy 18.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2007, v. 114, n. 7, p. 812, doi. 10.1111/j.1471-0528.2007.01349.x

By:

Jaques, A. M.;
Halliday, J. L.;
Francis, I.;
Bonacquisto, L.;
Forbes, R.;
Cronin, A.;
Sheffield, L. J.

Publication type:

Article

Second-trimester maternal serum inhibin A levels in fetal trisomy 18 and Turner syndrome with and without hydrops.

Published in:

Prenatal Diagnosis, 1998, v. 18, n. 10, p. 1061, doi. 10.1002/(SICI)1097-0223(199810)18:10<1061::AID-PD404>3.0.CO;2-M

By:

Lambert-Messerlian, G. M.;
Saller, D. N.;
Tumber, M. B.;
French, C. A.;
Peterson, C. J.;
Canick, J. A.

Publication type:

Article

HEAT-STABLE AND IMMUNOREACTIVE PLACENTAL ALKALINE PHOSPHATASE IN MATERNAL SERUM FROM DOWN'S SYNDROME AND TRISOMY 18 PREGNANCIES.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 11, p. 1051, doi. 10.1002/(SICI)1097-0223(199611)16:11<1051::AID-PD988>3.0.CO;2-T

By:

AITKEN, DAVID A.;
SYVERTSEN, BENTE S.;
CROSSLEY, JENNIFER A.;
BERRY, ESTHER;
CONNOR, J. MICHAEL

Publication type:

Article

Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45438-1

By:

Rohrlach, Adam Benjamin;
Rivollat, Maïté;
de-Miguel-Ibáñez, Patxuka;
Moilanen, Ulla;
Liira, Anne-Mari;
Teixeira, João C.;
Roca-Rada, Xavier;
Armendáriz-Martija, Javier;
Boyadzhiev, Kamen;
Boyadzhiev, Yavor;
Llamas, Bastien;
Tiliakou, Anthi;
Mötsch, Angela;
Tuke, Jonathan;
Prevedorou, Eleni-Anna;
Polychronakou-Sgouritsa, Naya;
Buikstra, Jane;
Onkamo, Päivi;
Stockhammer, Philipp W.;
Heyne, Henrike O.

Publication type:

Article

Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 46, doi. 10.1002/1097-0223(200101)21:1<46::AID-PD984>3.0.CO;2-C

By:

Benn, Peter A.;
Ying, Jun;
Beazoglou, Tryfon;
Egan, James F. X.

Publication type:

Article

Significant improvement in survival outcomes of trisomy 18 with neonatal intensive care compared to non-intensive care: a single-center study.

Published in:

PeerJ, 2023, p. 1, doi. 10.7717/peerj.16537

By:

Shigeki Koshida;
Kentaro Takahashi

Publication type:

Article

Trisomy 18 syndrome with congenital fibrotic change in the liver.

Published in:

Pediatrics International, 2006, v. 48, n. 6, p. 646, doi. 10.1111/j.1442-200X.2006.02286.x

By:

Maruyama, Kenichi;
Koizumi, Takenobu;
Hirato, Junko

Publication type:

Article

Antenatal reflex DNA screening for trisomy 18 and trisomy 13 in addition to Down’s syndrome.

Published in:

Journal of Medical Screening, 2016, v. 23, n. 4, p. 171, doi. 10.1177/0969141315617982

By:

Bestwick, Jonathan P.;
Wald, Nicholas J.

Publication type:

Article

Cardiac Surgical Repair Should Be Offered to Infants with Trisomy 18, Interrupted Aortic Arch and Ventricular Septal Defect.

Published in:

Journal of Law, Medicine & Ethics, 2016, v. 44, n. 2, p. 283, doi. 10.1177/1073110516654121

By:

Kavarana, Minoo N.

Publication type:

Article

孕中期超声联合无创产前基因筛查在检出染色体异常胎儿中的应用价值.

Published in:

Progress in Modern Biomedicine, 2023, v. 23, n. 17, p. 3382, doi. 10.13241/j.cnki.pmb.2023.17.035

By:

孙美云;
李扬;
文晓燕;
崔照领;
焦红燕;
封露露;
李强

Publication type:

Article

Trisomy 18 syndrome: case report.

Published in:

2012

By:

Karaman, Ali;
Khaveci, Hasan;
Laloglu, Fuat

Publication type:

Journal Article

Unusual Longevity of Edwards Syndrome: A Case Report.

Published in:

Genes, 2020, v. 11, n. 12, p. 1466, doi. 10.3390/genes11121466

By:

Alshami, Abbas;
Douedi, Steven;
Guida, Melissa;
Ajam, Firas;
Desai, Dhaval;
Zales, Vincent;
Calderon, Dawn M

Publication type:

Article

Prenatal Diagnosis of Cleft Lip and Palate: A Retrospective Study.

Published in:

Journal of Clinical Medicine, 2024, v. 13, n. 16, p. 4804, doi. 10.3390/jcm13164804

By:

Brăila, Anca Daniela;
Damian, Constantin Marian;
Albu, Cristina-Crenguţa;
Botoacă, Oana;
Dȋră, Laurențiu Mihai;
Albu, Ştefan-Dimitrie;
Brăila, Matei Georgian;
Bănățeanu, Andreea-Mariana;
Poalelungi, Cristian-Viorel;
Bogdan-Andreescu, Claudia Florina

Publication type:

Article

Everyone has a story to tell: The experiences of grandparents with a grandchild diagnosed with a genetic life-limiting condition.

Published in:

International Journal of Birth & Parent Education, 2015, v. 2, n. 3, p. 16

By:

Brown, Erica

Publication type:

Article

Detection of an Underlying 22q11.2 Duplication in a Female Neonate With Trisomy 18.

Published in:

Laboratory Medicine, 2017, v. 48, n. 4, p. 372, doi. 10.1093/labmed/lmx039

By:

Turbiville, Donald E.;
Hai Wu;
Jianli Dong

Publication type:

Article

The trisomy 18 syndrome.

Published in:

2012

By:

Cereda, Anna;
Carey, John C

Publication type:

journal article

The trisomy 18 syndrome.

Published in:

Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 81, doi. 10.1186/1750-1172-7-81

By:

Cereda, Anna;
Carey, John C.

Publication type:

Article

Fetal Tethered Spinal Cord: Diagnostic Features and Its Association with Congenital Anomalies.

Published in:

2023

By:

Yang, Xiaomei;
Sun, Shiyu;
Ji, Yizheng;
Xu, Yasong;
Sun, Li;
Wu, Qichang

Publication type:

Case Study

A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities.

Published in:

Fetal & Pediatric Pathology, 2021, v. 40, n. 3, p. 256, doi. 10.1080/15513815.2019.1695297

By:

Huang, Shufang;
Xia, Yu;
Ding, Hong;
Wang, Yonghua;
Wu, Yueheng;
Chen, Shaoxian;
Zhuang, Jian;
Li, Ping

Publication type:

Article

A visual tool inclusive of fetal ultrasound and autopsy findings to reach a balanced approach to counseling on trisomy 18 in early second trimester.

Published in:

Archives of Gynecology & Obstetrics, 2021, v. 304, n. 5, p. 1115, doi. 10.1007/s00404-021-06130-7

By:

Triunfo, Stefania;
Bonollo, Marta;
Gaffuri, Priska;
Viviano, Manuela;
Satta, Daniele;
Bergmann, Manuela

Publication type:

Article

Trysomy 18: an update on prenatal diagnosis and management. A case report.

Published in:

2017

By:

Dragan, I.;
Herghelegiu, C.;
Vladareanu, S.;
Moldoveanu, A.;
Oprescu, D.

Publication type:

Case Study

Clinical Image: A Case of Edwards' Syndrome.

Published in:

Journal of Neonatology, 2023, v. 37, n. 3, p. 282, doi. 10.1177/09732179221143197

By:

Muppa, Vikas;
Kar, Shrutiprajna;
Sahoo, Tanushree;
Sahoo, Sanjukta

Publication type:

Article

Failure to diagnose Trisomy 18 (Edwards' syndrome) from antenatal scan.

Published in:: Clinical Risk, 2011, v. 17, n. 5, p. 199, doi. 10.1258/cr.2010.010036
Publication type:: Article

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples.

Published in:

PLoS Computational Biology, 2021, v. 17, n. 12, p. 1, doi. 10.1371/journal.pcbi.1009684

By:

Paluoja, Priit;
Teder, Hindrek;
Ardeshirdavani, Amin;
Bayindir, Baran;
Vermeesch, Joris;
Salumets, Andres;
Krjutškov, Kaarel;
Palta, Priit

Publication type:

Article