Dória S - Search Results

1

Soares P, Rocha G, Pissarra S, Soares H, Flôr-de-Lima F, Costa S, Moura C, Dória S, Guimarães H. Soares P, et al. Among authors: doria s. Rev Port Cardiol. 2017 Mar;36(3):201-214. doi: 10.1016/j.repc.2016.10.007. Epub 2017 Feb 28. Rev Port Cardiol. 2017. PMID: 28256370 Free article. Review. English, Portuguese.

2

The role of DNA hydroxymethylation and TET enzymes in placental development and pregnancy outcome.

Vasconcelos S, Caniçais C, Chuva de Sousa Lopes SM, Marques CJ, Dória S. Vasconcelos S, et al. Among authors: doria s. Clin Epigenetics. 2023 Apr 25;15(1):66. doi: 10.1186/s13148-023-01483-z. Clin Epigenetics. 2023. PMID: 37095555 Free PMC article. Review.

3

New findings in partial trisomy 16q: clinical report.

Sousa B, Rocha G, Doria S, Alves JR, Guedes B, Guimarães H. Sousa B, et al. Among authors: doria s. Acta Paediatr. 2004 Jun;93(6):852-4. doi: 10.1111/j.1651-2227.2004.tb03032.x. Acta Paediatr. 2004. PMID: 15244241

4

Clinicopathological features of 45,X/46,Xidic(Y) mosaicism and therapeutic implications: case report.

Soares H, Maia A, Campos M, Dória S, Lopes JM, Fontoura M. Soares H, et al. Among authors: doria s. Sao Paulo Med J. 2008 Sep;126(5):297-9. doi: 10.1590/s1516-31802008000500012. Sao Paulo Med J. 2008. PMID: 19099167 Free article.

5

Array-CGH: importance in the study of developmental delays in pediatrics.

Pinheiro MI, Silva C, Lourenço L, Gonçalves D, Dória S, Guardiano M, Leão M. Pinheiro MI, et al. Among authors: doria s. Rev Neurol. 2020 Sep 1;71(5):171-176. doi: 10.33588/rn.7105.2020211. Rev Neurol. 2020. PMID: 32729108 Free article. English, Spanish.

6

Chronic eosinophilic leukaemia presenting with erythroderma, mild eosinophilia and hyper-IgE: clinical, immunological and cytogenetic features and therapeutic approach. A case report.

Granjo E, Lima M, Lopes JM, Dória S, Orfão A, Ying S, Barata LT, Miranda M, Cross NC, Bain BJ. Granjo E, et al. Among authors: doria s. Acta Haematol. 2002;107(2):108-12. doi: 10.1159/000046640. Acta Haematol. 2002. PMID: 11919392

7

Phenotypic expression in the first case of complete trisomy 12: combination of prenatal ultrasound and necropsic examination.

Machado AP, Ramalho C, Loureiro T, Cunha M, Dória S, Carvalho F, Oliveira JP, Brandão O, Matias A. Machado AP, et al. Among authors: doria s. Fetal Diagn Ther. 2009;25(2):234-8. doi: 10.1159/000222666. Epub 2009 Jun 3. Fetal Diagn Ther. 2009. PMID: 19494495

8

46,XX male disorder of sexual development.

Adrião M, Ferreira S, Silva RS, Garcia M, Dória S, Costa C, Castro-Correia C, Fontoura M. Adrião M, et al. Among authors: doria s. Clin Pediatr Endocrinol. 2020;29(1):43-45. doi: 10.1297/cpe.29.43. Epub 2020 Jan 9. Clin Pediatr Endocrinol. 2020. PMID: 32029971 Free PMC article.

9

Aneuploidies detection in miscarriages and fetal deaths using multiplex ligation-dependent probe amplification: an alternative for speeding up results?

Carvalho B, Dória S, Ramalho C, Brandão O, Sousa M, Matias A, Barros A, Carvalho F. Carvalho B, et al. Among authors: doria s. Eur J Obstet Gynecol Reprod Biol. 2010 Dec;153(2):151-5. doi: 10.1016/j.ejogrb.2010.06.022. Epub 2010 Aug 1. Eur J Obstet Gynecol Reprod Biol. 2010. PMID: 20678855

10

Inv21p12q22del21q22 and intellectual disability.

Oliveira R, Dória S, Madureira C, Lima V, Almeida C, Pinho MJ, Ramalho C, Matoso E, Barros A, Carreira IM, Moura CP. Oliveira R, et al. Among authors: doria s. Gene. 2013 Mar 15;517(1):120-4. doi: 10.1016/j.gene.2012.12.045. Epub 2012 Dec 20. Gene. 2013. PMID: 23266646

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