RONZONI, LUISA

RONZONI, LUISA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 57 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Adverse effect of PNPLA3 p.I148M genetic variant on kidney function in middle-aged individuals with metabolic dysfunction 2023 Pelusi, SerenaMalvestiti, FrancescoRonzoni, LuisaValenti, Luca + Article (author) -
Circulating indian hedgehog is a marker of the hepatocyte-TAZ pathway in experimental NASH and is elevated in humans with NASH 2023 Meroni, MaricaCherubini, AlessandroRonzoni, LuisaValenti, LucaDongiovanni, Paola + Article (author) -
SARS-CoV-2 infection in children: A 24 months experience with focus on risk factors in a pediatric tertiary care hospital in Milan, Italy 2023 Di Pietro, Giada MariaRonzoni, LuisaMeschia, Lorenzo MariaTagliabue, ClaudiaBosis, SamanthaMarchisio, Paola GiovannaValenti, Luca + Article (author) -
Clinical exome sequencing for diagnosing severe cryptogenic liver disease in adults: A case series 2022 Pelusi, SerenaRonzoni, LuisaMalvestiti, FrancescoD'Ambrosio, RobertaGiannotta, Juri AlessandroValenti, Luca + Article (author) -
Genetics: A new clinical tool for the hepatologist 2022 Valenti L.Ronzoni L. Article (author) -
Trends and risk factors of SARS-CoV-2 infection in asymptomatic blood donors 2021 Valenti L.Pelusi S.Ronzoni L.Uceda Renteria S.Malvestiti F. + Article (author) -
Incidence of chromosomal abnormalities in fetuses with first trimester ultrasound anomalies and a low-risk cell-free DNA test for common trisomies 2020 Persico N.Ischia B.Ronzoni L.Fabietti I.Silipigni R. + Article (author) -
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases 2017 A. TucciL. PezzaniG. ScuveraL. RonzoniS. EspositoD. Milani + Article (author) -
2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal Malformation 2017 Ronzoni L.Peron A.Triulzi F.Leva E. + Article (author) -
7p22.1 microduplication syndrome : refinement of the critical region 2017 L. RonzoniL. PezzaniA. TucciM. BaccarinS. EspositoD. Milani + Article (author) -
Ferroportin expression and regulation in non-transfusion dependent thalassemia 2016 L. SonzogniL. RonzoniG. GraziadeiM.D. Cappellini Article (author) -
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome 2016 A. TucciL. RonzoniS. EspositoD. Milani + Article (author) -
Growth differentiation factor 15 expression and regulation during erythroid differentiation in non-transfusion dependent thalassemia 2015 L. RonzoniL. SonzogniL. DucaG. GraziadeiM.D. Cappellini + Article (author) -
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins : a genotype-phenotype analysis 2015 L. RonzoniA. PeronM. BaccarinR. Silipigni + Article (author) -
Response to "Characteristics of 2p15-p16.1 microdeletion syndrome : review and description of two additional patients" 2015 L. RonzoniG. ScuveraS. EspositoD. Milani + Article (author) -
Modulation of gamma globin genes expression by histone deacetylase Inhibitors : an in vitro study 2014 L. RonzoniSONZOGNI, LAURAM.D. Cappellini + Article (author) -
Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase 2014 L. RonzoniM.D. Cappellini + Article (author) -
Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patients 2014 L. RonzoniA. AghemoM.G. RumiG. PratiA. ColanceccoS. MonicoM. ColomboM.D. Cappellini + Article (author) -
In vitro ferroportin expression in non trasfusion depedent thalassemia during erythroid differentiation 2013 L. SonzogniL. RonzoniA. MarconM.D. Cappellini + Article (author) -
Growth differentiation factor 15 expression and regulation during erythroid differentiation in non transfusion dependent thalassemia syndromes 2013 L. RonzoniL. SonzogniC. CesarettiA. MarconM.D. Cappellini + Article (author) -