Presi S - Search Results

1

Study on mutations and antiretroviral therapy (SMART): preliminary results.

Gianotti N, Moretti F, Tambussi G, Racca S, Presi S, Crucianelli R, Carrera P, Ferrari M, Lazzarin A. Gianotti N, et al. Among authors: presi s. Antivir Ther. 1999;4 Suppl 3:65-9. Antivir Ther. 1999. PMID: 16021873 Clinical Trial.

2

Molecular analysis of cerebrospinal fluid: potential for the study of HIV-1 infection of the central nervous system.

Cinque P, Bestetti A, Morelli P, Presi S. Cinque P, et al. Among authors: presi s. J Neurovirol. 2000 May;6 Suppl 1:S95-S102. J Neurovirol. 2000. PMID: 10871772 Review.

3

Effect of genotypic resistance on the virological response to highly active antiretroviral therapy in cerebrospinal fluid.

Cinque P, Presi S, Bestetti A, Pierotti C, Racca S, Boeri E, Morelli P, Carrera P, Ferrari M, Lazzarin A. Cinque P, et al. Among authors: presi s. AIDS Res Hum Retroviruses. 2001 Mar 20;17(5):377-83. doi: 10.1089/088922201750102409. AIDS Res Hum Retroviruses. 2001. PMID: 11282006

4

Long-term virological effect of highly active antiretroviral therapy on cerebrospinal fluid and relationship with genotypic resistance.

Bestetti A, Presi S, Pierotti C, Bossolasco S, Sala S, Racca S, Carrera P, Lazzarin A, Cinque P. Bestetti A, et al. Among authors: presi s. J Neurovirol. 2004;10 Suppl 1:52-7. doi: 10.1080/753312753. J Neurovirol. 2004. PMID: 14982740

5

Phylogenetic internal control for HIV-1 genotypic antiretroviral testing.

Boeri E, Canducci F, Grasso MA, Presi S, Carrera P, Racca S, Clementi M. Boeri E, et al. Among authors: presi s. New Microbiol. 2004 Apr;27(2 Suppl 1):105-9. New Microbiol. 2004. PMID: 15646072

6

Unexplained neonatal respiratory distress due to congenital surfactant deficiency.

Somaschini M, Nogee LM, Sassi I, Danhaive O, Presi S, Boldrini R, Montrasio C, Ferrari M, Wert SE, Carrera P. Somaschini M, et al. Among authors: presi s. J Pediatr. 2007 Jun;150(6):649-53, 653.e1. doi: 10.1016/j.jpeds.2007.03.008. J Pediatr. 2007. PMID: 17517255

7

Fatal respiratory failure in a full-term newborn with two ABCA3 gene mutations: a case report.

Ciantelli M, Ghirri P, Presi S, Sigali E, Vuerich M, Somaschini M, Ferrari M, Boldrini A, Carrera P. Ciantelli M, et al. Among authors: presi s. J Perinatol. 2011 Jan;31(1):70-2. doi: 10.1038/jp.2010.122. J Perinatol. 2011. PMID: 21189475

8

Genetic susceptibility to neonatal lung diseases.

Somaschini M, Castiglioni E, Presi S, Volonteri C, Ferrari M, Carrera P. Somaschini M, et al. Among authors: presi s. Acta Biomed. 2012;83 Suppl 1:10-4. Acta Biomed. 2012. PMID: 23029870

9

Null ABCA3 in humans: large homozygous ABCA3 deletion, correlation to clinical-pathological findings.

Carrera P, Ferrari M, Presi S, Ventura L, Vergani B, Lucchini V, Cogo PE, Carnielli VP, Somaschini M, Tagliabue P. Carrera P, et al. Among authors: presi s. Pediatr Pulmonol. 2014 Mar;49(3):E116-20. doi: 10.1002/ppul.22983. Epub 2014 Jan 14. Pediatr Pulmonol. 2014. PMID: 24420869

10

Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome.

Somaschini M, Presi S, Ferrari M, Vergani B, Carrera P. Somaschini M, et al. Among authors: presi s. J Perinatol. 2018 Apr;38(4):337-344. doi: 10.1038/s41372-017-0018-2. Epub 2017 Dec 19. J Perinatol. 2018. PMID: 29255193 Free PMC article.

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