S. Presi

发表

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

B. Vergani, M. Ferrari, P. Carrera, 2017, Journal of Perinatology.

Null ABCA3 in humans: Large homozygous ABCA3 deletion, correlation to clinical–pathological findings

B. Vergani, M. Ferrari, P. Cogo, 2014, Pediatric pulmonology.

Genetic surfactant dysfunction in newborn infants and children with acute and chronic lung disease

B. Vergani, M. Ferrari, P. Carrera, 2017 .

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

A. Lazzarin, P. Cinque, S. Bossolasco, 2011, Journal of NeuroVirology.

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

A. Lazzarin, P. Cinque, P. Carrera, 2001, AIDS research and human retroviruses.

Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches

C. Di Resta, M. Ferrari, G. Querques, 2018, EJIFCC.

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

P. Cinque, S. Presi, A. Bestetti, 2000, Journal of neurovirology.

Novel JAG1 Deletion Variant in Patient with Atypical Alagille Syndrome

C. Pappone, E. Locati, M. Ferrari, 2019, International journal of molecular sciences.

Unexplained neonatal respiratory distress due to congenital surfactant deficiency.

R. Boldrini, M. Ferrari, O. Danhaive, 2007, The Journal of pediatrics.

Deep tissue biopsy vs. superficial swab culture monitoring in the microbiological assessment of limb‐threatening diabetic foot infection

M. Strazzabosco, P. Benedetti, F. de Lalla, 2001, Diabetic medicine : a journal of the British Diabetic Association.

APC-Related Phenotypes and Intellectual Disability in 5q Interstitial Deletions: A New Case and Review of the Literature

M. P. Recalcati, Flavia Piccini, Paola Carrera, 2023, Genes.

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

P. Cinque, S. Presi, P. Morelli, 2000, Journal of neurovirology.

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

M. Vuerich, A. Boldrini, P. Ghirri, 2011, Journal of Perinatology.

Molecular cloning, expression and purification of protein 2A of hepatitis A virus.

M. Clementi, F. Canducci, P. Carrera, 2004, The new microbiologica.

Phylogenetic internal control for HIV-1 genotypic antiretroviral testing.

M. Clementi, F. Canducci, P. Carrera, 2004, The new microbiologica.

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

I. Rivolta, I. Polsinelli, S. Ricagno, 2023, International journal of molecular sciences.

Germline pathogenic variants of cancer predisposition genes in a multicentre Italian cohort of pancreatic cancer patients.

L. Archibugi, W. Bruno, M. Macchini, 2024, European Journal of Cancer.