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Results: 1 to 20 of 289

1.

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

Bestwick JP, Wald NJ.

J Med Screen. 2015 Apr 14. pii: 0969141315575545. [Epub ahead of print]

PMID:
25872932
2.

Medical procedures and outcomes of Japanese patients with trisomy 18 or trisomy 13: Analysis of a nationwide administrative database of hospitalized patients.

Ishitsuka K, Matsui H, Michihata N, Fushimi K, Nakamura T, Yasunaga H.

Am J Med Genet A. 2015 Apr 5. doi: 10.1002/ajmg.a.37104. [Epub ahead of print]

PMID:
25847518
3.

Developmental status of 22 children with trisomy 18 and eight children with trisomy 13: Implications and recommendations.

Bruns DA.

Am J Med Genet A. 2015 Apr 5. doi: 10.1002/ajmg.a.37102. [Epub ahead of print]

PMID:
25847310
4.

Intractable Nodulocystic Acne in a Patient with Trisomy 13.

Peart JM, Licht DJ, Prange EO, Treat JR.

Pediatr Dermatol. 2015 Jan 30. doi: 10.1111/pde.12511. [Epub ahead of print]

PMID:
25639329
5.

A Contemporary, Single-Institutional Experience of Surgical Versus Expectant Management of Congenital Heart Disease in Trisomy 13 and 18 Patients.

Costello JP, Weiderhold A, Louis C, Shaughnessy C, Peer SM, Zurakowski D, Jonas RA, Nath DS.

Pediatr Cardiol. 2015 Jan 23. [Epub ahead of print]

PMID:
25612784
6.
7.

Natural history of fetal trisomy 13 after prenatal diagnosis.

Barry SC, Walsh CA, Burke AL, McParland P, McAuliffe FM, Morrison JJ.

Am J Med Genet A. 2015 Jan;167A(1):147-50. doi: 10.1002/ajmg.a.36824. Epub 2014 Oct 22.

PMID:
25339456
8.

Nine children over the age of one year with full trisomy 13: a case series describing medical conditions.

Bruns DA, Campbell E.

Am J Med Genet A. 2014 Dec;164A(12):2987-95. doi: 10.1002/ajmg.a.36689. Epub 2014 Oct 16.

PMID:
25323598
9.

[Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center].

Naor Dovev M, Maymon R, Keidar R, Reish O, Melcer Y, Vaknin Z.

Harefuah. 2014 Aug;153(8):453-7, 499, 498. Hebrew. Erratum in: Harefuah. 2014 Dec;153(12):751. Meltzer, Y [corrected to Melcer, Y].

PMID:
25286634
10.

Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central Africa.

Mbuyi-Musanzayi S, Lumaka A, Yogolelo Asani B, Lubala Kasole T, Lukusa Tshilobo P, Kalenga Muenze P, Tshilombo Katombe F, Devriendt K.

Case Rep Genet. 2014;2014:365031. doi: 10.1155/2014/365031. Epub 2014 Sep 1.

11.

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma.

Gekas J, Langlois S, Ravitsky V, Audibert F, van den Berg DG, Haidar H, Rousseau F.

Appl Clin Genet. 2014 Jul 7;7:127-31. doi: 10.2147/TACG.S35602. eCollection 2014. Review.

12.

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

Springett AL, Morris JK.

J Med Screen. 2014 Sep;21(3):113-9. doi: 10.1177/0969141314543128. Epub 2014 Jul 3.

PMID:
24993362
13.

Cytogenetically normal acute myeloid leukemia with a novel KIT mutation in exon 11 G565V developing a sole trisomy 13 at relapse: a clinical dilemma.

Nieto MJ, Scalise A, Najfeld V.

Acta Haematol. 2015;133(1):1-5. doi: 10.1159/000360389. Epub 2014 Jun 21.

PMID:
24968822
14.

Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis.

Herold T, Metzeler KH, Vosberg S, Hartmann L, Röllig C, Stölzel F, Schneider S, Hubmann M, Zellmeier E, Ksienzyk B, Jurinovic V, Pasalic Z, Kakadia PM, Dufour A, Graf A, Krebs S, Blum H, Sauerland MC, Büchner T, Berdel WE, Woermann BJ, Bornhäuser M, Ehninger G, Mansmann U, Hiddemann W, Bohlander SK, Spiekermann K, Greif PA.

Blood. 2014 Aug 21;124(8):1304-11. doi: 10.1182/blood-2013-12-540716. Epub 2014 Jun 12.

PMID:
24923295
15.

A patient with trisomy 13 mosaicism with an unusual skin pigmentary pattern and prolonged survival.

González-del Angel A, Estandia-Ortega B, Gaviño-Vergara A, Sáez-de-Ocariz M, Velasco-Hernández Mde L, Salas-Labadía C.

Pediatr Dermatol. 2014 Sep-Oct;31(5):580-3. doi: 10.1111/pde.12339. Epub 2014 May 20.

PMID:
24846410
16.

Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.

Hall MP, Hill M, Zimmermann B, Sigurjonsson S, Westemeyer M, Saucier J, Demko Z, Rabinowitz M.

PLoS One. 2014 May 7;9(5):e96677. doi: 10.1371/journal.pone.0096677. eCollection 2014.

17.

Non-invasive prenatal testing for trisomy 13: more harm than good?

Verweij EJ, de Boer MA, Oepkes D.

Ultrasound Obstet Gynecol. 2014 Jul;44(1):112-4. doi: 10.1002/uog.13388.

PMID:
24753041
18.

Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testing.

Liu XY, Zhang HG, Wang RX, Chen S, Yu XW, Liu RZ.

J Assist Reprod Genet. 2014 May;31(5):589-94. doi: 10.1007/s10815-014-0182-7. Epub 2014 Feb 5.

19.

A newborn with trisomy 13 who had tetralogy of Fallot and metopic synostosis: Case report.

Karabel M, Yolbaş I, Kelekçi S, Sen V, Haspolat Y, Timuroğlu L.

Hippokratia. 2013 Jul;17(3):268-70.

20.

Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18.

Boghossian NS, Hansen NI, Bell EF, Stoll BJ, Murray JC, Carey JC, Adams-Chapman I, Shankaran S, Walsh MC, Laptook AR, Faix RG, Newman NS, Hale EC, Das A, Wilson LD, Hensman AM, Grisby C, Collins MV, Vasil DM, Finkle J, Maffett D, Ball MB, Lacy CB, Bara R, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

Pediatrics. 2014 Feb;133(2):226-35. doi: 10.1542/peds.2013-1702. Epub 2014 Jan 20.

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