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Stefano Duga

Showing results (81-90 of 141) with videos related to

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Minerva Urology and Nephrology|January 13, 2021
Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, ItalyMassimo Lazzeri, Stefano Duga, Elena Azzolini, et al.
Parkinsonism & Related Disorders|May 13, 2014
LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian populationRoberto Cilia, Chiara Siri, Damiana Rusconi, et al.
Neurology. Genetics|November 19, 2020
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PDLetizia Straniero, Rosanna Asselta, Salvatore Bonvegna, et al.
Neurobiology of Aging|January 12, 2010
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease geneIlaria Guella, Anna Pistocchi, Rosanna Asselta, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Multiple Sclerosis and Related Disorders|November 29, 2022
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profileGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Frontiers in Oncology|June 10, 2021
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and BiologyMarinella Corbetta, Chiara Chiereghin, Ilaria De Simone, et al.
Haematologica|November 9, 2019
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart diseaseElvezia Maria Paraboschi, Amit Vikram Khera, Piera Angelica Merlini, et al.
Frontiers in Cell and Developmental Biology|December 13, 2021
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic DiseaseMatteo Vecellio, Elvezia Maria Paraboschi, Angela Ceribelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2020
Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement DisordersWai Yan Yau, Jana Vandrovcova, Roisin Sullivan, et al.
Pageof 15

Showing results (81-90 of 141) with videos related to

Sort By:
Pageof 15
Minerva Urology and Nephrology|January 13, 2021
Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, ItalyMassimo Lazzeri, Stefano Duga, Elena Azzolini, et al.
Parkinsonism & Related Disorders|May 13, 2014
LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian populationRoberto Cilia, Chiara Siri, Damiana Rusconi, et al.
Neurology. Genetics|November 19, 2020
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PDLetizia Straniero, Rosanna Asselta, Salvatore Bonvegna, et al.
Neurobiology of Aging|January 12, 2010
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease geneIlaria Guella, Anna Pistocchi, Rosanna Asselta, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Multiple Sclerosis and Related Disorders|November 29, 2022
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profileGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Frontiers in Oncology|June 10, 2021
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and BiologyMarinella Corbetta, Chiara Chiereghin, Ilaria De Simone, et al.
Haematologica|November 9, 2019
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart diseaseElvezia Maria Paraboschi, Amit Vikram Khera, Piera Angelica Merlini, et al.
Frontiers in Cell and Developmental Biology|December 13, 2021
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic DiseaseMatteo Vecellio, Elvezia Maria Paraboschi, Angela Ceribelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2020
Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement DisordersWai Yan Yau, Jana Vandrovcova, Roisin Sullivan, et al.
Pageof 15