Caracas, cadáver exquisito

od Duga Picharde Albarracín
Wydane w Revista Venezolana de Economía y Ciencias Sociales (2010)

Hereditary Hypofibrinogenemia with Hepatic Storage

od Rosanna Asselta, Elvezia Maria Paraboschi, Stefano Duga
Wydane 2020-10-01

Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains

od Paraboschi, Elvezia Maria, Duga, Stefano, Asselta, Rosanna
Wydane w Int J Mol Sci (2017)

Hereditary Hypofibrinogenemia with Hepatic Storage

od Asselta, Rosanna, Paraboschi, Elvezia Maria, Duga, Stefano
Wydane w Int J Mol Sci (2020)

Support groups for people carrying a BRCA mutation

od Dorval, Michel, Maunsell, Elizabeth, Duga, Michel J., Simard, Jacques
Wydane 2001

ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

od Asselta, Rosanna, Paraboschi, Elvezia Maria, Mantovani, Alberto, Duga, Stefano
Wydane w Aging (Albany NY) (2020)

Editorial: RNA Splicing and Backsplicing: Disease and Therapy

od Asselta, Rosanna, Duga, Stefano, Velasco, Eladio Andrés, Buratti, Emanuele
Wydane w Front Genet (2020)

Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions

od Paraboschi, Elvezia Maria, Cardamone, Giulia, Soldà, Giulia, Duga, Stefano, Asselta, Rosanna
Wydane w Front Genet (2018)

Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency

od Paraboschi, Elvezia Maria, Menegatti, Marzia, Peyvandi, Flora, Duga, Stefano, Asselta, Rosanna
Wydane w Int J Mol Sci (2019)

cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex.

od Simonic, T, Duga, S, Negri, A, Tedeschi, G, Malcovati, M, Tenchini, M L, Ronchi, S
Wydane 1997

Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype

od Szabo, Andras, Czako, Marta, Hadzsiev, Kinga, Duga, Balazs, Komlosi, Katalin, Melegh, Bela
Wydane w Mol Cytogenet (2015)

The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis

od Cardamone, Giulia, Paraboschi, Elvezia Maria, Rimoldi, Valeria, Duga, Stefano, Soldà, Giulia, Asselta, Rosanna
Wydane w Int J Mol Sci (2017)

Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients

od Cardamone, Giulia, Paraboschi, Elvezia Maria, Soldà, Giulia, Duga, Stefano, Saarela, Janna, Asselta, Rosanna
Wydane w Biomedicines (2018)

Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript

od Rimoldi, Valeria, Soldà, Giulia, Asselta, Rosanna, Spena, Silvia, Stuani, Cristiana, Buratti, Emanuele, Duga, Stefano
Wydane 2013

Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome

od Komlósi, Katalin, Duga, Balázs, Hadzsiev, Kinga, Czakó, Márta, Kosztolányi, György, Fogarasi, András, Melegh, Béla
Wydane w Mol Cytogenet (2015)

First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features

od Straniero, Letizia, Rimoldi, Valeria, Soldà, Giulia, Bellini, Melissa, Biasucci, Giacomo, Asselta, Rosanna, Duga, Stefano
Wydane w Front Genet (2018)

Drug use evaluation in pregnant women attending antenatal care in Shashemene Referral Hospital, Oromia Regional State, Ethiopia

od Geresu, Gudeta Duga, Sondesa, Dirirsa Tashome, Yadesa, Tadele Mekuriya, Mtewa, Andrew G, Abebe, Bontu Aschale
Wydane w SAGE Open Med (2020)

First Independent Replication of the Involvement of LARS2 in Perrault Syndrome by Whole-Exome Sequencing of an Italian Family

od Soldà, Giulia, Caccia, Sonia, Robusto, Michela, Chiereghin, Chiara, Castorina, Pierangela, Ambrosetti, Umberto, Duga, Stefano, Asselta, Rosanna
Wydane w J Hum Genet (2015)

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes

od Paraboschi, Elvezia Maria, Cardamone, Giulia, Rimoldi, Valeria, Gemmati, Donato, Spreafico, Marta, Duga, Stefano, Soldà, Giulia, Asselta, Rosanna
Wydane w Int J Mol Sci (2015)

A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

od Soldà, Giulia, Robusto, Michela, Primignani, Paola, Castorina, Pierangela, Benzoni, Elena, Cesarani, Antonio, Ambrosetti, Umberto, Asselta, Rosanna, Duga, Stefano
Wydane 2012