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Items: 1 to 20 of 54

1.

Solid Phase Formylation of N-Terminus Peptides.

Tornesello AL, Sanseverino M, Buonaguro FM.

Molecules. 2016 Jun 4;21(6). pii: E736. doi: 10.3390/molecules21060736.

2.

Zika virus: A new human teratogen? Implications for women of reproductive age.

Schuler-Faccini L, Sanseverino M, Vianna F, da Silva AA, Larrandaburu M, Marcolongo-Pereira C, Abeche AM.

Clin Pharmacol Ther. 2016 Jul;100(1):28-30. doi: 10.1002/cpt.386. Epub 2016 May 13.

PMID:
27090438
3.

New Findings in eNOS gene and Thalidomide Embryopathy Suggest pre-transcriptional effect variants as susceptibility factors.

Kowalski TW, Fraga LR, Tovo-Rodrigues L, Sanseverino MT, Hutz MH, Schuler-Faccini L, Vianna FS.

Sci Rep. 2016 Mar 23;6:23404. doi: 10.1038/srep23404.

4.

Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015.

Schuler-Faccini L, Ribeiro EM, Feitosa IM, Horovitz DD, Cavalcanti DP, Pessoa A, Doriqui MJ, Neri JI, Neto JM, Wanderley HY, Cernach M, El-Husny AS, Pone MV, Serao CL, Sanseverino MT; Brazilian Medical Genetics Society–Zika Embryopathy Task Force.

MMWR Morb Mortal Wkly Rep. 2016 Jan 29;65(3):59-62. doi: 10.15585/mmwr.mm6503e2.

5.

A new hexapeptide from the leader peptide of rMnSOD enters cells through the oestrogen receptor to deliver therapeutic molecules.

Borrelli A, Schiattarella A, Mancini R, Pica A, Pollio ML, Ruggiero MG, Bonelli P, De Luca V, Tuccillo FM, Capasso C, Gori E, Sanseverino M, Carpentieri A, Birolo L, Pucci P, Rommelaere J, Mancini A.

Sci Rep. 2016 Jan 4;6:18691. doi: 10.1038/srep18691.

6.

Primary prevention of neural tube defects in Brazil: insights into anencephaly.

Bronberg R, Dipierri J, Alfaro E, Sanseverino MT, Schüler-Faccini L.

J Community Genet. 2016 Jan;7(1):97-105. doi: 10.1007/s12687-015-0249-x. Epub 2015 Aug 18. No abstract available.

7.

[Prevalence of congenital abnormalities identified in fetuses with 13, 18 and 21 chromosomal trisomy].

Emer CS, Duque JA, Müller AL, Gus R, Sanseverino MT, da Silva AA, Magalhães JA.

Rev Bras Ginecol Obstet. 2015 Jul;37(7):333-8. doi: 10.1590/S0100-720320150005373. Portuguese.

8.

Thalidomide embryopathy: Follow-up of cases born between 1959 and 2010.

Kowalski TW, Sanseverino MT, Schuler-Faccini L, Vianna FS.

Birth Defects Res A Clin Mol Teratol. 2015 Sep;103(9):794-803. doi: 10.1002/bdra.23376. Epub 2015 Jun 4.

PMID:
26043318
9.

Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.

Larrandaburu M, Matte U, Noble A, Olivera Z, Sanseverino MT, Nacul L, Schuler-Faccini L.

J Community Genet. 2015 Jul;6(3):241-9. doi: 10.1007/s12687-015-0236-2. Epub 2015 May 29.

10.

Nonelective surgery at night and in-hospital mortality: Prospective observational data from the European Surgical Outcomes Study.

van Zaane B, van Klei WA, Buhre WF, Bauer P, Boerma EC, Hoeft A, Metnitz P, Moreno RP, Pearse R, Pelosi P, Sander M, Vallet B, Pettilä V, Vincent JL, Rhodes A; European Surgical Outcomes Study (EuSOS) group for the Trials groups of the European Society of Intensive Care Medicine and the European Society of Anaesthesiology.

Eur J Anaesthesiol. 2015 Jul;32(7):477-85. doi: 10.1097/EJA.0000000000000256.

PMID:
26001104
11.

Clinical and molecular characterization of a Brazilian cohort of campomelic dysplasia patients, and identification of seven new SOX9 mutations.

Mattos EP, Sanseverino MT, Magalhães JA, Leite JC, Félix TM, Todeschini LA, Cavalcanti DP, Schüler-Faccini L.

Genet Mol Biol. 2015 Mar;38(1):14-20. doi: 10.1590/S1415-475738120140147. Epub 2014 Mar 17.

12.

Identification of a premature stop codon mutation in the PHGDH gene in severe Neu-Laxova syndrome-evidence for phenotypic variability.

Mattos EP, Silva AA, Magalhães JA, Leite JC, Leistner-Segal S, Gus-Kessler R, Perez JA, Vedolin LM, Torreblanca-Zanca A, Lapunzina P, Ruiz-Perez VL, Sanseverino MT.

Am J Med Genet A. 2015 Jun;167(6):1323-9. doi: 10.1002/ajmg.a.36930. Epub 2015 Apr 25.

PMID:
25913727
13.

Pharmacoepidemiology and thalidomide embryopathy surveillance in Brazil.

Sales Luiz Vianna F, de Oliveira MZ, Sanseverino MT, Morelo EF, de Lyra Rabello Neto D, Lopez-Camelo J, Camey SA, Schuler-Faccini L.

Reprod Toxicol. 2015 Jun;53:63-7. doi: 10.1016/j.reprotox.2015.03.007. Epub 2015 Mar 28.

PMID:
25828060
14.

Interaction between TP63 and MDM2 genes and the risk of recurrent pregnancy loss.

Fraga LR, Boquett JA, Dutra CG, Vianna FS, Heck C, Gonçalves RO, Paskulin DD, Costa OL, Ashton-Prolla P, Sanseverino MT, Schuler-Faccini L.

Eur J Obstet Gynecol Reprod Biol. 2014 Nov;182:7-10. doi: 10.1016/j.ejogrb.2014.07.044. Epub 2014 Aug 24.

PMID:
25218545
15.

Albumin replacement in patients with severe sepsis or septic shock.

Caironi P, Tognoni G, Masson S, Fumagalli R, Pesenti A, Romero M, Fanizza C, Caspani L, Faenza S, Grasselli G, Iapichino G, Antonelli M, Parrini V, Fiore G, Latini R, Gattinoni L; ALBIOS Study Investigators.

N Engl J Med. 2014 Apr 10;370(15):1412-21. doi: 10.1056/NEJMoa1305727. Epub 2014 Mar 18.

16.

Lack of association between thrombophilic gene variants and recurrent pregnancy loss.

Dutra CG, Fraga LR, Nácul AP, Passos EP, Gonçalves RO, Nunes OL, De Godoy BA, Leistner-Segal S, Vianna FS, Schüler-Faccini L, Sanseverino MT.

Hum Fertil (Camb). 2014 Jun;17(2):99-105. doi: 10.3109/14647273.2014.882022. Epub 2014 Feb 24.

PMID:
24564524
17.

Impact on pregnancies in south Brazil from the influenza A (H1N1) pandemic: cohort study.

da Silva AA, Ranieri TM, Torres FD, Vianna FS, Paniz GR, Sanseverino PB, Picon PD, de Azevedo PB, Costa MH, Schuler-Faccini L, Sanseverino MT.

PLoS One. 2014 Feb 18;9(2):e88624. doi: 10.1371/journal.pone.0088624. eCollection 2014.

18.

[Associated factors for perinatal mortality in gastroschisis].

Calcagnotto H, Müller AL, Leite JC, Sanseverino MT, Gomes KW, Magalhães JA.

Rev Bras Ginecol Obstet. 2013 Dec;35(12):549-53. Portuguese.

19.

p53 signaling pathway polymorphisms associated to recurrent pregnancy loss.

Fraga LR, Dutra CG, Boquett JA, Vianna FS, Gonçalves RO, Paskulin DD, Costa OL, Ashton-Prolla P, Sanseverino MT, Schuler-Faccini L.

Mol Biol Rep. 2014 Mar;41(3):1871-7. doi: 10.1007/s11033-014-3036-6. Epub 2014 Jan 17.

PMID:
24435975
20.

Polymorphisms in the endothelial nitric oxide synthase gene in thalidomide embryopathy.

Vianna FS, Fraga LR, Tovo-Rodrigues L, Tagliani-Ribeiro A, Biondi F, Maximino CM, Sanseverino MT, Hutz MH, Schuler-Faccini L.

Nitric Oxide. 2013 Nov 30;35:89-92. doi: 10.1016/j.niox.2013.09.002. Epub 2013 Sep 17.

PMID:
24055736
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