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[22q11.2 deletion syndrome: importance of clinical evaluation and FISH analysis].
Koshiyama DB, Rosa RF, Zen PR, Pereira VL, Graziadio C, Cóser VM, Ricachinevsky CP, Varella-Garcia M, Paskulin GA. Koshiyama DB, et al. Rev Assoc Med Bras (1992). 2009 Jul-Aug;55(4):442-6. doi: 10.1590/s0104-42302009000400020. Rev Assoc Med Bras (1992). 2009. PMID: 19750312 Free article. Portuguese.
[22q11.2 deletion syndrome and complex congenital heart defects].
Rosa RF, Trevisan P, Koshiyama DB, Pilla CB, Zen PR, Varella-Garcia M, Paskulin GA. Rosa RF, et al. Among authors: koshiyama db. Rev Assoc Med Bras (1992). 2011 Jan-Feb;57(1):62-5. Rev Assoc Med Bras (1992). 2011. PMID: 21390462 Free article. Portuguese.
Frequency and clinical significance of chromosome 7 and 10 aneuploidies, amplification of the EGFR gene, deletion of PTEN and TP53 genes, and 1p/19q deficiency in a sample of adult patients diagnosed with glioblastoma from Southern Brazil.
Koshiyama DB, Trevisan P, Graziadio C, Rosa RFM, Cunegatto B, Scholl J, Provenzi VO, de Sá AP, Soares FP, Velho MC, de A P Filho N, Oliveira CA, Zen PRG. Koshiyama DB, et al. J Neurooncol. 2017 Dec;135(3):465-472. doi: 10.1007/s11060-017-2606-6. Epub 2017 Aug 30. J Neurooncol. 2017. PMID: 28856550
Chromosomal abnormalities in patients with congenital heart disease.
Trevisan P, Zen TD, Rosa RF, Silva JN, Koshiyama DB, Paskulin GA, Zen PR. Trevisan P, et al. Among authors: koshiyama db. Arq Bras Cardiol. 2013 Dec;101(6):495-501. doi: 10.5935/abc.20130204. Epub 2013 Oct 22. Arq Bras Cardiol. 2013. PMID: 24145389 Free PMC article.