GASPARINI, PAOLO

GASPARINI, PAOLO  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss 2021 Giannuzzi, GiulianaGasparini, Paolo + Article (author) -
Primary ciliary dyskinesia: the impact of taste receptors (TAS2R38) gene polymorphisms on disease outcome and severity 2020 G. PiattiU. AmbrosettiA. RobinoP. Gasparini + Article (author) -
Action observation therapy in pediatric patients with neuromotor deficits of the upper limbs secondary to central nervous system tumors 2019 Sensi R.Clerici C. A.Gariboldi F. A.Spreafico F.Schiavello E.Gasparini P.Caraceni A. T.Ferrari A. + Article (author) -
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 2018 Giri A.Menni C.Gasparini P.Johansson A.Robino A.Ruggiero D. + Article (author) -
Poor outcome from acute upper gastrointestinal bleeding in patients with liver cirrhosis: a prospective multicenter observational study 2016 Bargiggia, S.Dell'Era, A.Tortora, A.Segato, S.Parravicini, M.Bucci, C.Baldassarre, G.Gasparini, P.Franceschi, M.Masci, E.Antoniazzi, S.Ferraris, L.Lauri, A.De Stefano, S.De Franchis, R. + Article (author) -
The Italian node of the research infrastructure BBMRI 2011 Catalano M.Gasparini P. + Article (author) -
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy 2009 Ghezzi D.Gasparini P.Ferrero I. + Article (author) -
Analisis of HLA-H mutations in italian patients with genetic hemochromatosis: Evidence of genetic heterogeneity 1997 Sampietro M.Vergani A.Arosio C.Fracanzani A. L.Gasparini P.Fargion S. + Article (author) -