Sartorato EL - Search Results

1

Contribution of the GSTP1 c.313A>G variant to hearing loss risk in patients exposed to platin chemotherapy during childhood.

Liberman PHP, Goffi-Gomez MVS, Schultz C, Jacob PL, de Paula CAA, Sartorato EL, Torrezan GT, Ferreira EN, Carraro DM. Liberman PHP, et al. Among authors: sartorato el. Clin Transl Oncol. 2019 May;21(5):630-635. doi: 10.1007/s12094-018-1964-7. Epub 2018 Oct 25. Clin Transl Oncol. 2019. PMID: 30361796

2

Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.

Alves RM, da Silva Costa SM, do Amôr Divino Miranda PM, Ramos PZ, Marconi TG, Santos Oliveira G, Castilho AM, Sartorato EL. Alves RM, et al. Among authors: sartorato el. BMC Med Genet. 2016 May 26;17(1):41. doi: 10.1186/s12881-016-0303-5. BMC Med Genet. 2016. PMID: 27230773 Free PMC article.

3

Molecular study of patients with auditory neuropathy.

Carvalho GM, Ramos PZ, Castilho AM, Guimarães AC, Sartorato EL. Carvalho GM, et al. Among authors: sartorato el. Mol Med Rep. 2016 Jul;14(1):481-90. doi: 10.3892/mmr.2016.5226. Epub 2016 May 9. Mol Med Rep. 2016. PMID: 27177047

4

Etiologic and diagnostic evaluation: algorithm for severe to profound sensorineural hearing loss in Brazil.

Ramos PZ, de Moraes VC, Svidnicki MC, Soki MN, Castilho AM, Sartorato EL. Ramos PZ, et al. Among authors: sartorato el. Int J Audiol. 2013 Nov;52(11):746-52. doi: 10.3109/14992027.2013.817689. Epub 2013 Aug 3. Int J Audiol. 2013. PMID: 23909750

5

Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology.

Svidnicki MC, Silva-Costa SM, Ramos PZ, dos Santos NZ, Martins FT, Castilho AM, Sartorato EL. Svidnicki MC, et al. Among authors: sartorato el. BMC Med Genet. 2015 Sep 23;16:85. doi: 10.1186/s12881-015-0232-8. BMC Med Genet. 2015. PMID: 26399936 Free PMC article.

6

Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform.

Martins FT, Ramos PZ, Svidnicki MC, Castilho AM, Sartorato EL. Martins FT, et al. Among authors: sartorato el. BMC Med Genet. 2013 Oct 24;14:112. doi: 10.1186/1471-2350-14-112. BMC Med Genet. 2013. PMID: 24156272 Free PMC article.

7

Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.

de Moraes VC, dos Santos NZ, Ramos PZ, Svidnicki MC, Castilho AM, Sartorato EL. de Moraes VC, et al. Among authors: sartorato el. Int J Pediatr Otorhinolaryngol. 2013 Mar;77(3):410-3. doi: 10.1016/j.ijporl.2012.11.042. Epub 2012 Dec 27. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23273637

8

Connexin mutations in Brazilian patients with skin disorders with or without hearing loss.

Alexandrino F, de Oliveira CA, Magalhães RF, Florence ME, de Souza EM, Sartorato EL. Alexandrino F, et al. Among authors: sartorato el. Am J Med Genet A. 2009 Feb 15;149A(4):681-4. doi: 10.1002/ajmg.a.32765. Am J Med Genet A. 2009. PMID: 19283857

9

Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment.

de Moraes VC, Alexandrino F, Andrade PB, Câmara MF, Sartorato EL. de Moraes VC, et al. Among authors: sartorato el. Biochem Biophys Res Commun. 2009 Apr 3;381(2):210-3. doi: 10.1016/j.bbrc.2009.02.014. Epub 2009 Feb 12. Biochem Biophys Res Commun. 2009. PMID: 19338775 Free article.

10

Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss.

Grillo AP, de Oliveira FM, de Carvalho GQ, Medrano RF, da Silva-Costa SM, Sartorato EL, de Oliveira CA. Grillo AP, et al. Among authors: sartorato el. Biomed Res Int. 2015;2015:318727. doi: 10.1155/2015/318727. Epub 2015 May 17. Biomed Res Int. 2015. PMID: 26075227 Free PMC article. Clinical Trial.

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