Ferrari I - Search Results

1

GATA1 mutations in acute leukemia in children with Down syndrome.

Magalhães IQ, Splendore A, Emerenciano M, Figueiredo A, Ferrari I, Pombo-de-Oliveira MS. Magalhães IQ, et al. Among authors: ferrari i. Cancer Genet Cytogenet. 2006 Apr 15;166(2):112-6. doi: 10.1016/j.cancergencyto.2005.10.008. Cancer Genet Cytogenet. 2006. PMID: 16631466

2

Transient neonatal myeloproliferative disorder without Down syndrome and detection of GATA1 mutation.

Magalhães IQ, Splendore A, Emerenciano M, Córdoba MS, Córdoba JC, Allemand PA, Ferrari I, Pombo-de-Oliveira MS. Magalhães IQ, et al. Among authors: ferrari i. J Pediatr Hematol Oncol. 2005 Jan;27(1):50-2. doi: 10.1097/01.mph.0000151801.26478.03. J Pediatr Hematol Oncol. 2005. PMID: 15654280

3

Molecular and chromosomal mutations among children with B-lineage lymphoblastic leukemia in Brazil's Federal District.

Mesquita DR, Córdoba JC, Magalhães IQ, Córdoba MS, Oliveira JR, Gonçalves A, Ferrari I, Martins-de-Sá C. Mesquita DR, et al. Among authors: ferrari i. Genet Mol Res. 2009 Mar 24;8(1):345-53. doi: 10.4238/vol8-1gmr582. Genet Mol Res. 2009. PMID: 19440970 Free article.

4

Analysis of GATA1 mutations and leukemogenesis in newborns with Down syndrome.

Queiroz LB, Lima BD, Mazzeu JF, Camargo R, Córdoba MS, Q Magalhães I, Martins-de-Sá C, Ferrari I. Queiroz LB, et al. Among authors: ferrari i. Genet Mol Res. 2013 Oct 18;12(4):4630-8. doi: 10.4238/2013.October.18.1. Genet Mol Res. 2013. PMID: 24222239 Free article.

5

Costello syndrome in two Brazilian children.

Pratesi R, Santos M, Ferrari I. Pratesi R, et al. Among authors: ferrari i. J Med Genet. 1998 Jan;35(1):54-7. doi: 10.1136/jmg.35.1.54. J Med Genet. 1998. PMID: 9475096 Free PMC article. Review.

6

Response to treatment with imatinib mesylate in previously treated chronic-phase chronic myeloid leukemia patients in a hospital in Brazil.

Silveira CA, Daldegan MB, Ferrari I. Silveira CA, et al. Among authors: ferrari i. Genet Mol Res. 2011 Sep 15;10(3):2038-48. doi: 10.4238/vol10-3gmr1073. Genet Mol Res. 2011. PMID: 21968620 Free article.

7

Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum.

Dos Santos PA, de Oliveira SF, Freitas EL, Safatle HP, Rosenberg C, Ferrari I, Mazzeu JF. Dos Santos PA, et al. Among authors: ferrari i. Am J Med Genet A. 2014 Feb;164A(2):551-3. doi: 10.1002/ajmg.a.36231. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311469 No abstract available.

8

Complex phenotype associated with 17q21.31 microdeletion.

Dornelles-Wawruk H, Pic-Taylor A, Rosenberg C, Krepischi AC, Safatle HP, Ferrari I, Mazzeu JF. Dornelles-Wawruk H, et al. Among authors: ferrari i. Mol Syndromol. 2013 Sep;4(6):297-301. doi: 10.1159/000354120. Epub 2013 Aug 21. Mol Syndromol. 2013. PMID: 24167466 Free PMC article.

9

Partial AFF2 microduplication in a patient with auditory processing disorder, emotional impairment and macrosomia.

da Rocha NB, dos Santos PA, Safatle HP, de Melo RM, Pereira RW, de Oliveira SF, Pic-Taylor A, Ferrari I, Mazzeu JF. da Rocha NB, et al. Among authors: ferrari i. Am J Med Genet A. 2014 Dec;164A(12):3206-8. doi: 10.1002/ajmg.a.36768. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25256661 No abstract available.

10

Transient neonatal hypothyroidism in a boy with unbalanced translocation t(8;16).

Secchi LA, Mazzeu JF, Córdoba MS, Ferrari I, Ramos HE, Neves Fde A. Secchi LA, et al. Among authors: ferrari i. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):564-9. doi: 10.1590/s0004-27302012000800017. Arq Bras Endocrinol Metabol. 2012. PMID: 23295299

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