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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 1
1969 1
1972 1
1975 1
1977 2
1981 2
1982 2
1985 2
1987 2
1988 4
1989 2
1990 6
1991 5
1992 7
1993 7
1994 8
1995 14
1996 13
1997 9
1998 10
1999 8
2000 11
2001 9
2002 4
2003 4
2004 4
2005 11
2006 10
2007 9
2008 5
2009 14
2010 7
2011 14
2012 9
2013 8
2014 13
2015 17
2016 17
2017 16
2018 17
2019 16
2020 12
2021 15
2022 11
2023 9
2024 4

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344 results

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Page 1
Triploid pregnancy-Clinical implications.
Massalska D, Bijok J, Kucińska-Chahwan A, Zimowski JG, Ozdarska K, Panek G, Roszkowski T. Massalska D, et al. Clin Genet. 2021 Oct;100(4):368-375. doi: 10.1111/cge.14003. Epub 2021 Jun 1. Clin Genet. 2021. PMID: 34031868 Review.
Triploidy is a life-limiting genetic aberration resulting from an extra haploid set of chromosomes of paternal (diandric triploidy) or maternal origin (digynic triploidy). Triploidy affects around 1%-2% of all conceptions. The majority of cases is misc …
Triploidy is a life-limiting genetic aberration resulting from an extra haploid set of chromosomes of paternal (diandric triploidy …
Hydatidiform mole.
Daumová M, Hadravská Š, Putzová M. Daumová M, et al. Cesk Patol. 2023 Summer;59(2):50-54. Cesk Patol. 2023. PMID: 37468322 English.
Prognostic impact of chromosomal abnormalities and copy number alterations in adult B-cell precursor acute lymphoblastic leukaemia: a UKALL14 study.
Moorman AV, Barretta E, Butler ER, Ward EJ, Twentyman K, Kirkwood AA, Enshaei A, Schwab C, Creasey T, Leongamornlert D, Papaemmanuil E, Patrick P, Clifton-Hadley L, Patel B, Menne T, McMillan AK, Harrison CJ, Rowntree CJ, Marks DI, Fielding AK. Moorman AV, et al. Leukemia. 2022 Mar;36(3):625-636. doi: 10.1038/s41375-021-01448-2. Epub 2021 Oct 16. Leukemia. 2022. PMID: 34657128 Free PMC article. Clinical Trial.
Patients with KMT2A-AFF1, complex karyotype (CK) and low hypodiploidy/near-triploidy (HoTr) had high relapse rates 50%, 60% & 53% and correspondingly poor survival. ...
Patients with KMT2A-AFF1, complex karyotype (CK) and low hypodiploidy/near-triploidy (HoTr) had high relapse rates 50%, 60% & 53% …
Long-term follow-up of salvage therapy using a combination of inotuzumab ozogamicin and mini-hyper-CVD with or without blinatumomab in relapsed/refractory Philadelphia chromosome-negative acute lymphoblastic leukemia.
Jabbour E, Sasaki K, Short NJ, Ravandi F, Huang X, Khoury JD, Kanagal-Shamanna R, Jorgensen J, Khouri IF, Kebriaei P, Jain N, Alvarado Y, Kadia TM, Paul S, Garcia-Manero G, Dabaja BS, Burger JA, DiNardo CD, Daver NA, Montalban-Bravo G, Yilmaz M, Ohanian M, Ferrajoli A, Jacob J, Rostykus M, Garris R, O'Brien S, Kantarjian HM. Jabbour E, et al. Cancer. 2021 Jun 15;127(12):2025-2038. doi: 10.1002/cncr.33469. Epub 2021 Mar 19. Cancer. 2021. PMID: 33740268 Free article.
The 3-year OS rate for patients with CD22 expression 70% and without adverse cytogenetics (KMT2A rearrangements, low hypodiploidy/near triploidy) was 55%. CONCLUSION: The combination of inotuzumab and low-intensity mini-hyper-CVD chemotherapy with or without blinatumomab s …
The 3-year OS rate for patients with CD22 expression 70% and without adverse cytogenetics (KMT2A rearrangements, low hypodiploidy/near tr …
First trimester combined screening - focus on early biochemistry.
Tørring N. Tørring N. Scand J Clin Lab Invest. 2016 Oct;76(6):435-47. doi: 10.1080/00365513.2016.1200131. Epub 2016 Jul 12. Scand J Clin Lab Invest. 2016. PMID: 27403933 Review.
Improvements in the algorithm have extended the screening to include trisomy 21 in mono- and dichorionic twin pregnancies, trisomy 18, trisomy 13 and triploidy. The results from large databases have shown that the screening algorithms are efficient for a range of rare auto …
Improvements in the algorithm have extended the screening to include trisomy 21 in mono- and dichorionic twin pregnancies, trisomy 18, triso …
Distribution of diandric and digynic triploidy depending on gestational age.
Massalska D, Ozdarska K, Roszkowski T, Bijok J, Kucińska-Chahwan A, Panek GM, Zimowski JG. Massalska D, et al. J Assist Reprod Genet. 2021 Sep;38(9):2391-2395. doi: 10.1007/s10815-021-02202-4. Epub 2021 May 13. J Assist Reprod Genet. 2021. PMID: 33982170 Free PMC article. Clinical Trial.
PURPOSE: To establish the distribution of diandric and digynic triploidy depending on gestational age. METHODS: 107 triploid samples tested prospectively in a single genetic department during a four-year period were analyzed for parental origin of triploidy by Quant …
PURPOSE: To establish the distribution of diandric and digynic triploidy depending on gestational age. METHODS: 107 triploid samples …
Hydatidiform moles: ancillary techniques to refine diagnosis.
Ronnett BM, DeScipio C, Murphy KM. Ronnett BM, et al. Int J Gynecol Pathol. 2011 Mar;30(2):101-16. doi: 10.1097/PGP.0b013e3181f4de77. Int J Gynecol Pathol. 2011. PMID: 21293291 Review.
The unique genetic features of CHMs (androgenetic diploidy), PHMs (diandric triploidy), and nonmolar specimens (biparental diploidy) allow for certain molecular techniques, including immunohistochemical analysis of p57 expression (a paternally imprinted maternally expresse …
The unique genetic features of CHMs (androgenetic diploidy), PHMs (diandric triploidy), and nonmolar specimens (biparental diploidy) …
Posttest risk calculation following positive noninvasive prenatal screening using cell-free DNA in maternal plasma.
Benn P. Benn P. Am J Obstet Gynecol. 2016 Jun;214(6):676.e1-7. doi: 10.1016/j.ajog.2016.01.003. Epub 2016 Jan 7. Am J Obstet Gynecol. 2016. PMID: 26772793 Review.
For example, commonly used rates for trisomy 13, monosomy-X, triploidy, and 22q11.2 deletion syndrome can vary by >4-fold and this can translate into large differences in PTR. ...
For example, commonly used rates for trisomy 13, monosomy-X, triploidy, and 22q11.2 deletion syndrome can vary by >4-fold and this …
Stillborn Infants: Associated Malformations.
Holmes LB, Nasri H, Beroukhim R, Hunt AT, Roberts DJ, Toufaily MH, Westgate MN. Holmes LB, et al. Birth Defects Res. 2018 Jan;110(2):114-121. doi: 10.1002/bdr2.1097. Birth Defects Res. 2018. PMID: 29377646
RESULTS: One hundred twenty-seven stillborn infants with malformations were identified at autopsy among 289,365 pregnancies, including trisomies 21, 18, and 13; 45,X; triploidy; anencephaly; lower urinary tract obstruction; holoprosencephaly and severe heart defects, such …
RESULTS: One hundred twenty-seven stillborn infants with malformations were identified at autopsy among 289,365 pregnancies, including triso …
344 results