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Brain : a Journal of Neurology
|
November 1, 2017
The multiple faces of TOR1A: different inheritance, different phenotype
Monia Ginevrino, Enza Maria Valente
Parkinsonism & Related Disorders
|
September 6, 2015
Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models
Simona Petrucci, Monia Ginevrino, Enza Maria Valente
BMC Neurology
|
January 13, 2021
Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
Marina Picillo, Sara Scannapieco, Alessandro Iavarone, et al.
Movement Disorders Clinical Practice
|
October 12, 2020
<i>APP</i>-Related Corticobasal Syndrome: Expanding the List of Corticobasal Degeneration Look Alikes
Filomena Abate, Giovanna Dati, Monia Ginevrino, et al.
European Journal of Human Genetics : EJHG
|
May 26, 2018
Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype
Sara Nuovo, Alessia Micalizzi, Stefano D'Arrigo, et al.
Journal of the Neurological Sciences
|
April 9, 2018
Intrafamilial variability in a polish family harbouring a frameshift THAP1 mutation
Maria Stamelou, Simona Petrucci, Monia Ginevrino, et al.
Neurogenetics
|
June 3, 2016
Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutation
Alessia Micalizzi, Isabella Moroni, Monia Ginevrino, et al.
Pediatric Rheumatology Online Journal
|
January 18, 2024
Monogenic systemic lupus erythematosus onset in a 13-year-old boy with Noonan like-syndrome: a case report and literature review
Patricia Morán-Álvarez, Alessandra Gianviti, Francesca Diomedi-Camassei, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
October 1, 2020
Gamma-transcranial alternating current stimulation and theta-burst stimulation: inter-subject variability and the role of BDNF
Andrea Guerra, Francesco Asci, Alessandro Zampogna, et al.
Molecular Biology Reports
|
October 5, 2019
A novel IRF2BPL truncating variant is associated with endolysosomal storage
Monia Ginevrino, Roberta Battini, Sara Nuovo, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Brain : a Journal of Neurology
|
November 1, 2017
The multiple faces of TOR1A: different inheritance, different phenotype
Monia Ginevrino, Enza Maria Valente
Parkinsonism & Related Disorders
|
September 6, 2015
Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models
Simona Petrucci, Monia Ginevrino, Enza Maria Valente
BMC Neurology
|
January 13, 2021
Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
Marina Picillo, Sara Scannapieco, Alessandro Iavarone, et al.
Movement Disorders Clinical Practice
|
October 12, 2020
<i>APP</i>-Related Corticobasal Syndrome: Expanding the List of Corticobasal Degeneration Look Alikes
Filomena Abate, Giovanna Dati, Monia Ginevrino, et al.
European Journal of Human Genetics : EJHG
|
May 26, 2018
Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype
Sara Nuovo, Alessia Micalizzi, Stefano D'Arrigo, et al.
Journal of the Neurological Sciences
|
April 9, 2018
Intrafamilial variability in a polish family harbouring a frameshift THAP1 mutation
Maria Stamelou, Simona Petrucci, Monia Ginevrino, et al.
Neurogenetics
|
June 3, 2016
Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutation
Alessia Micalizzi, Isabella Moroni, Monia Ginevrino, et al.
Pediatric Rheumatology Online Journal
|
January 18, 2024
Monogenic systemic lupus erythematosus onset in a 13-year-old boy with Noonan like-syndrome: a case report and literature review
Patricia Morán-Álvarez, Alessandra Gianviti, Francesca Diomedi-Camassei, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
October 1, 2020
Gamma-transcranial alternating current stimulation and theta-burst stimulation: inter-subject variability and the role of BDNF
Andrea Guerra, Francesco Asci, Alessandro Zampogna, et al.
Molecular Biology Reports
|
October 5, 2019
A novel IRF2BPL truncating variant is associated with endolysosomal storage
Monia Ginevrino, Roberta Battini, Sara Nuovo, et al.
Page
of 4