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Year Number of Results
1988 2
1993 1
1994 1
2007 1
2012 1
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2017 1
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2022 1
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11 results

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Page 1
Isolating fetal cells in maternal circulation for prenatal diagnosis.
Simpson JL, Elias S. Simpson JL, et al. Prenat Diagn. 1994 Dec;14(13):1229-42. doi: 10.1002/pd.1970141308. Prenat Diagn. 1994. PMID: 7617569 Review.
Chromosomal abnormalities detected on isolated fetal cells include trisomy 21, trisomy 18, Klinefelter syndrome (47,XXY) and 47,XYY. Polymerase chain reaction (PCR) technology has enabled the detection of fetal sex, Mendelian disorders (e.g. beta-globin mutations), …
Chromosomal abnormalities detected on isolated fetal cells include trisomy 21, trisomy 18, Klinefelter syndrome (47,XXY) and 4 …
Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience.
Lau TK, Chan MK, Lo PS, Chan HY, Chan WS, Koo TY, Ng HY, Pooh RK. Lau TK, et al. J Matern Fetal Neonatal Med. 2012 Oct;25(10):1856-9. doi: 10.3109/14767058.2012.678442. Epub 2012 Apr 28. J Matern Fetal Neonatal Med. 2012. PMID: 22471583 Free PMC article.
The test was positive for trisomy 21 in eight cases, and for trisomy 18 in 1 case; all were confirmed by fetal karyotyping. There was no false-positive result. Of the questionnaires, 182 completed responses were received. Over 95% had complete or almos …
The test was positive for trisomy 21 in eight cases, and for trisomy 18 in 1 case; all were confirmed by fetal karyotyping. Th …
First- and second-trimester screening: detection of aneuploidies other than Down syndrome.
Breathnach FM, Malone FD, Lambert-Messerlian G, Cuckle HS, Porter TF, Nyberg DA, Comstock CH, Saade GR, Berkowitz RL, Klugman S, Dugoff L, Craigo SD, Timor-Tritsch IE, Carr SR, Wolfe HM, Tripp T, Bianchi DW, D'Alton ME; First and Second Trimester Evaluation of Risk (FASTER) Research Consortium. Breathnach FM, et al. Obstet Gynecol. 2007 Sep;110(3):651-7. doi: 10.1097/01.AOG.0000278570.76392.a6. Obstet Gynecol. 2007. PMID: 17766613
Risk cutoff levels of 1:300 for Down syndrome and 1:100 for trisomy 18 were selected. RESULTS: Thirty-six thousand one hundred seventy-one patients completed first-trimester screening, and 35,236 completed second-trimester screening. ...In second-trime …
Risk cutoff levels of 1:300 for Down syndrome and 1:100 for trisomy 18 were selected. RESULTS: Thirty-six thousand one hundred …
Prenatal diagnosis of congenital heart disease and fetal karyotyping.
Paladini D, Calabrò R, Palmieri S, D'Andrea T. Paladini D, et al. Obstet Gynecol. 1993 May;81(5 ( Pt 1)):679-82. Obstet Gynecol. 1993. PMID: 8469453
RESULTS: Congenital heart disease was found in 31 of 469 fetuses with complete follow-up. Fifteen of these 31 fetuses (48%) were found to have an abnormal karyotype: five of 17 (29.4%) with isolated cardiac anomalies and ten of 14 (71.4%) with cardiac and extracardiac anom …
RESULTS: Congenital heart disease was found in 31 of 469 fetuses with complete follow-up. Fifteen of these 31 fetuses (48%) were foun …
Audit of the first > 7500 noninvasive prenatal aneuploidy tests in a Swiss genetics center.
Bajka A, Bajka M, Chablais F, Burkhardt T. Bajka A, et al. Arch Gynecol Obstet. 2022 May;305(5):1185-1192. doi: 10.1007/s00404-021-06203-7. Epub 2021 Sep 17. Arch Gynecol Obstet. 2022. PMID: 34533609 Free PMC article.
OBJECTIVES: Noninvasive prenatal testing (NIPT) is actually the most accurate method of screening for fetal chromosomal aberration (FCA). We used pregnancy outcome record to evaluate a complete data set of single nucleotide polymorphism-based test results performed by a Sw …
OBJECTIVES: Noninvasive prenatal testing (NIPT) is actually the most accurate method of screening for fetal chromosomal aberration (FCA). We …
The Role Of Surgical Treatment In The Multidisciplinary Therapy For Hepatoblastoma.
Yada K, Ishibashi H, Mori H, Sato H, Shimada M. Yada K, et al. Hepatogastroenterology. 2014 May;61(131):553-6. Hepatogastroenterology. 2014. PMID: 26176034
Our therapeutic protocol included neoadjuvant chemotherapy (NAC) + hepatectomy + adjuvant chemotherapy (AC). ...One case with 18 trisomy underwent right hepatectomy for PRETEXT II HB and is still doing well 67 months after hepatectomy. CONCLUSIONS: It was found that multid …
Our therapeutic protocol included neoadjuvant chemotherapy (NAC) + hepatectomy + adjuvant chemotherapy (AC). ...One case with 18 tris …
Efficacy of prenatal ultrasonography in diagnosing urogenital developmental anomalies in newborns.
Beke A, Eros FR, Pete B, Szabo I, Gorbe E, Rigo J Jr. Beke A, et al. BMC Pregnancy Childbirth. 2014 Feb 24;14:82. doi: 10.1186/1471-2393-14-82. BMC Pregnancy Childbirth. 2014. PMID: 24564681 Free PMC article.
RESULTS: Prenatal sonographic diagnosis and postnatal results completely coincided in 45%, i.e. 63/140 of cases in newborns delivered with urogenital developmental disorders. ...In four newborns, chromosomal aberration was associated with the urogenital disorder; 45,X kary …
RESULTS: Prenatal sonographic diagnosis and postnatal results completely coincided in 45%, i.e. 63/140 of cases in newborns delivered …
The Dandy-Walker malformation prenatal sonographic diagnosis and its clinical significance.
Nyberg DA, Cyr DR, Mack LA, Fitzsimmons J, Hickok D, Mahony BS. Nyberg DA, et al. J Ultrasound Med. 1988 Feb;7(2):65-71. doi: 10.7863/jum.1988.7.2.65. J Ultrasound Med. 1988. PMID: 3279226
To determine the usual sonographic findings and clinical significance of the Dandy-Walker malformation (DWM) identified in utero, we reviewed seven proven cases diagnosed by prenatal ultrasound during a 6-year period. All patients demonstrated complete or partial absence o …
To determine the usual sonographic findings and clinical significance of the Dandy-Walker malformation (DWM) identified in utero, we reviewe …
Management of gastric mucosa-associated lymphoid tissue lymphoma in patients with extra copies of the MALT1 gene.
Iwamuro M, Takenaka R, Nakagawa M, Moritou Y, Saito S, Hori S, Inaba T, Kawai Y, Toyokawa T, Tanaka T, Yoshino T, Okada H. Iwamuro M, et al. World J Gastroenterol. 2017 Sep 7;23(33):6155-6163. doi: 10.3748/wjg.v23.i33.6155. World J Gastroenterol. 2017. PMID: 28970731 Free PMC article.
Mean ages and clinical stages at lymphoma diagnosis were not different between groups. Complete response was obtained in 61 patients in Group A (69.3%), 22 in Group B (81.5%), and 21 in Group C (67.7%). Helicobacter pylori (H. pylori) eradication alone resulted in compl …
Mean ages and clinical stages at lymphoma diagnosis were not different between groups. Complete response was obtained in 61 patients …
Amniotic fluid alpha-fetoprotein levels and prenatal diagnosis of autosomal trisomies.
Kaffe S, Perlis TE, Hsu LY. Kaffe S, et al. Prenat Diagn. 1988 Mar;8(3):183-7. doi: 10.1002/pd.1970080304. Prenat Diagn. 1988. PMID: 2453867
This observation led to the suggestion that low AFAFP levels be used as a criterion for completion of a chromosomal analysis in patients who are not otherwise at increased risk for a fetal chromosome abnormality and in whom karyotyping might not have been completed …
This observation led to the suggestion that low AFAFP levels be used as a criterion for completion of a chromosomal analysis in patie …
11 results