Maciel-Guerra AT - Search Results

1

Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.

Amaral-Fernandes MS, Marcondes AM, do Amor Divino Miranda PM, Maciel-Guerra AT, Sartorato EL. Amaral-Fernandes MS, et al. Mol Vis. 2011;17:3175-9. Epub 2011 Dec 7. Mol Vis. 2011. PMID: 22194643 Free PMC article.

2

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.

de Oliveira FR, Mazzola TN, de Mello MP, Francese-Santos AP, Lemos-Marini SHV, Maciel-Guerra AT, Hiort O, Werner R, Guerra-Junior G, Fabbri-Scallet H. de Oliveira FR, et al. Among authors: maciel guerra at. Life (Basel). 2023 Apr 27;13(5):1093. doi: 10.3390/life13051093. Life (Basel). 2023. PMID: 37240737 Free PMC article.

3

Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.

Riccetto L, Vieira TP, Viguetti-Campos NL, Mazzola TN, Guaragna MS, Fabbri-Scallet H, Mello MP, Marques-de-Faria AP, Maciel-Guerra AT, Guerra Junior G. Riccetto L, et al. Among authors: maciel guerra at. Sao Paulo Med J. 2022 Nov 28;141(4):e2022281. doi: 10.1590/1516-3180.2022.0281.R1.30082022. eCollection 2022. Sao Paulo Med J. 2022. PMID: 36449967 Free PMC article.

4

Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil.

Cursino KA, Garcia GM, Barros BA, Mazzola TN, Fabbri-Scallet H, Guaragna MS, Vieira TAP, Mello MP, Maciel-Guerra AT, Guerra-Junior G. Cursino KA, et al. Among authors: maciel guerra at. Fetal Diagn Ther. 2024;51(1):49-54. doi: 10.1159/000534401. Epub 2023 Oct 4. Fetal Diagn Ther. 2024. PMID: 37793360

5

DHX37 and the Implications in Disorders of Sex Development: An Update Review.

de Oliveira FR, Guaragna MS, Maciel-Guerra AT, Barros BA, de Mello MP, Guerra-Junior G, Fabbri-Scallet H. de Oliveira FR, et al. Among authors: maciel guerra at. Horm Res Paediatr. 2024;97(5):433-444. doi: 10.1159/000535969. Epub 2023 Dec 23. Horm Res Paediatr. 2024. PMID: 38142677 Free article. Review.

6

Determination of the frequency of the 35delG allele in Brazilian neonates.

Sartorato EL, Gottardi E, de Oliveira CA, Magna LA, Annichino-Bizzacchi JM, Seixas CA, Maciel-Guerra AT. Sartorato EL, et al. Clin Genet. 2000 Oct;58(4):339-40. doi: 10.1034/j.1399-0004.2000.580415.x. Clin Genet. 2000. PMID: 11076062 No abstract available.

7

Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients.

Oliveira CA, Maciel-Guerra AT, Sartorato EL. Oliveira CA, et al. Clin Genet. 2002 May;61(5):354-8. doi: 10.1034/j.1399-0004.2002.610506.x. Clin Genet. 2002. PMID: 12081719

8

Screening for mutations in the GJB3 gene in Brazilian patients with nonsyndromic deafness.

Alexandrino F, Oliveira CA, Reis FC, Maciel-Guerra AT, Sartorato EL. Alexandrino F, et al. J Appl Genet. 2004;45(2):249-54. J Appl Genet. 2004. PMID: 15131355

9

Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.

Oliveira CA, Alexandrino F, Abe-Sandes K, Silva WA Jr, Maciel-Guerra AT, Magna LA, Sartorato EL. Oliveira CA, et al. Hum Biol. 2004 Apr;76(2):313-6. doi: 10.1353/hub.2004.0035. Hum Biol. 2004. PMID: 15359540

10

Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions.

Oliveira CA, Pimpinati CJ, Alexandrino F, Magna LA, Maciel-Guerra AT, Sartorato EL. Oliveira CA, et al. Genet Test. 2007 Spring;11(1):1-3. doi: 10.1089/gte.2006.9994. Genet Test. 2007. PMID: 17394388

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