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Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):955-964. doi: 10.1002/ajmg.c.31860. Epub 2020 Nov 30.
Am J Med Genet C Semin Med Genet. 2020.
PMID: 33258288
Primary ovary choriocarcinoma: individual DNA polymorphic analysis as a strategy to confirm diagnosis and treatment.
Exman P, Takahashi TK, Gattás GF, Cantagalli VD, Anton C, Nalesso F, Diz Mdel P.
Exman P, et al. Among authors: cantagalli vd.
Rare Tumors. 2013 Jun 13;5(2):89-92. doi: 10.4081/rt.2013.e24. Print 2013 Apr 15.
Rare Tumors. 2013.
PMID: 23888224
Free PMC article.
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Granulocyte-macrophage colony-stimulating factor gene based therapy for acute limb ischemia in a mouse model.
Sacramento CB, Cantagalli VD, Grings M, Carvalho LP, Baptista-Silva JC, Beutel A, Bergamaschi CT, de Campos Junior RR, de Moraes JZ, Takiya CM, Samoto VY, Borojevic R, da Silva FH, Nardi NB, Dohmann HF, Junior HS, Valero VB, Han SW.
Sacramento CB, et al. Among authors: cantagalli vd.
J Gene Med. 2009 Apr;11(4):345-53. doi: 10.1002/jgm.1298.
J Gene Med. 2009.
PMID: 19194978
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