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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, Italy
Massimo 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 population
Roberto Cilia, Chiara Siri, Damiana Rusconi, et al.
Neurology. Genetics
|
November 19, 2020
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD
Letizia 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 gene
Ilaria Guella, Anna Pistocchi, Rosanna Asselta, et al.
Parkinsonism & Related Disorders
|
March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy
Edoardo 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 profile
Giulia 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 Biology
Marinella 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 disease
Elvezia 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 Disease
Matteo 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 Disorders
Wai Yan Yau, Jana Vandrovcova, Roisin Sullivan, et al.
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Search research articles
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Showing results (81-90 of 141) with videos related to
Sort By:
Page
of 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, Italy
Massimo 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 population
Roberto Cilia, Chiara Siri, Damiana Rusconi, et al.
Neurology. Genetics
|
November 19, 2020
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD
Letizia 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 gene
Ilaria Guella, Anna Pistocchi, Rosanna Asselta, et al.
Parkinsonism & Related Disorders
|
March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy
Edoardo 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 profile
Giulia 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 Biology
Marinella 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 disease
Elvezia 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 Disease
Matteo 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 Disorders
Wai Yan Yau, Jana Vandrovcova, Roisin Sullivan, et al.
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of 15