Takeno SS - Search Results

1

Congenital adrenal hyperplasia, ovarian failure and Ehlers-Danlos syndrome due to a 6p deletion.

Moysés-Oliveira M, Mancini TI, Takeno SS, Rodrigues AD, Bachega TA, Bertola D, Melaragno MI. Moysés-Oliveira M, et al. Among authors: takeno ss. Sex Dev. 2014;8(4):139-45. doi: 10.1159/000363779. Epub 2014 Jun 26. Sex Dev. 2014. PMID: 24970489

2

Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene.

Colovati ME, da Silva LR, Takeno SS, Mancini TI, N Dutra AR, Guilherme RS, de Mello CB, Melaragno MI, A Perez AB. Colovati ME, et al. Among authors: takeno ss. Mol Cytogenet. 2012 Jan 19;5:5. doi: 10.1186/1755-8166-5-5. Mol Cytogenet. 2012. PMID: 22260333 Free PMC article.

3

Clinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.

Guilherme RS, Bragagnolo S, Pellegrino R, Christofolini DM, Takeno SS, Carvolheira GM, Kulikowski LD, Melaragno MI. Guilherme RS, et al. Among authors: takeno ss. Cytogenet Genome Res. 2011;134(4):325-30. doi: 10.1159/000329478. Epub 2011 Aug 17. Cytogenet Genome Res. 2011. PMID: 21849783 Review.

4

Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features.

Mancini TI, Oliveira MM, Dutra AR, Perez AB, Minillo RM, Takeno SS, Melaragno MI. Mancini TI, et al. Among authors: takeno ss. Mol Syndromol. 2012 Jun;3(1):39-43. doi: 10.1159/000338468. Epub 2012 May 11. Mol Syndromol. 2012. PMID: 22855654 Free PMC article.

5

19q13.33→qter trisomy in a girl with intellectual impairment and seizures.

Carvalheira G, Oliveira MM, Takeno S, Lima FT, Meloni VA, Melaragno MI. Carvalheira G, et al. Meta Gene. 2014 Oct 27;2:799-806. doi: 10.1016/j.mgene.2014.09.004. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606462 Free PMC article.

6

Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.

Takeno SS, Corbani M, Andrade JA, Smith Mde A, Brunoni D, Melaragno MI. Takeno SS, et al. Am J Med Genet A. 2004 Aug 30;129A(2):180-3. doi: 10.1002/ajmg.a.30224. Am J Med Genet A. 2004. PMID: 15316961

7

A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.

Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI. Guilherme RS, et al. Among authors: takeno ss. Cytogenet Genome Res. 2013;141(4):317-23. doi: 10.1159/000353302. Epub 2013 Jun 29. Cytogenet Genome Res. 2013. PMID: 23817307

8

Intellectual, adaptive and behavioural characteristics in four patients with 18p deletion syndrome.

Mello CB, Bueno OFA, Benedetto LM, Pimenta LSE, Takeno SS, Melaragno MI, Meloni VA. Mello CB, et al. Among authors: takeno ss. J Intellect Disabil Res. 2019 Mar;63(3):225-232. doi: 10.1111/jir.12568. Epub 2018 Dec 9. J Intellect Disabil Res. 2019. PMID: 30536814

9

First report of a small supernumerary der(8;14) marker chromosome.

Guilherme RS, Dutra AR, Perez AB, Takeno SS, Oliveira MM, Kulikowski LD, Klein E, Hamid AB, Liehr T, Melaragno MI. Guilherme RS, et al. Among authors: takeno ss. Cytogenet Genome Res. 2013;139(4):284-8. doi: 10.1159/000348743. Epub 2013 Mar 23. Cytogenet Genome Res. 2013. PMID: 23548553

10

Identification of IL11RA and MELK amplification in gastric cancer by comprehensive genomic profiling of gastric cancer cell lines.

Calcagno DQ, Takeno SS, Gigek CO, Leal MF, Wisnieski F, Chen ES, Araújo TM, Lima EM, Melaragno MI, Demachki S, Assumpção PP, Burbano RR, Smith MC. Calcagno DQ, et al. Among authors: takeno ss. World J Gastroenterol. 2016 Nov 21;22(43):9506-9514. doi: 10.3748/wjg.v22.i43.9506. World J Gastroenterol. 2016. PMID: 27920471 Free PMC article.

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