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Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2021
THAP1 Dystonia with Globus Pallidus T2 Hypointensity: A Report of Two Cases
Giovanna Zorzi, Federica R Danti, Chiara Reale, et al.
Frontiers in Genetics
|
March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts
Maria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
BMC Neurology
|
April 2, 2020
Idiopathic brain calcification in a patient with hereditary hemochromatosis
Stefania Scarlini, Francesco Cavallieri, Massimo Fiorini, et al.
Neurogenetics
|
August 13, 2021
Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activation
Chiara Cavestro, Celeste Panteghini, Chiara Reale, et al.
Parkinsonism & Related Disorders
|
February 21, 2026
Early-onset parkinsonism with intellectual disability in an Italian family associated with a PTRHD1 variant
Giuseppe Pedullà, Maurizio Morelli, Paola Soliveri, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 30, 2022
Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome
Claudia M Bonardi, Allan Bayat, Camilla Gøbel Madsen, et al.
Parkinsonism & Related Disorders
|
October 2, 2022
ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcome
Giulia Straccia, Chiara Reale, Massimo Castellani, et al.
European Journal of Neurology
|
March 14, 2022
DNAJB2-related Charcot-Marie-Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening
Paola Saveri, Stefania Magri, Emanuela Maderna, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2016
DYT2 screening in early-onset isolated dystonia
Miryam Carecchio, Chiara Reale, Federica Invernizzi, et al.
Epilepsia
|
October 28, 2024
Quantitative EEG biomarkers for STXBP1-related disorders
Alberto Cossu, Francesca Furia, Jacopo Proietti, et al.
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Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2021
THAP1 Dystonia with Globus Pallidus T2 Hypointensity: A Report of Two Cases
Giovanna Zorzi, Federica R Danti, Chiara Reale, et al.
Frontiers in Genetics
|
March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts
Maria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
BMC Neurology
|
April 2, 2020
Idiopathic brain calcification in a patient with hereditary hemochromatosis
Stefania Scarlini, Francesco Cavallieri, Massimo Fiorini, et al.
Neurogenetics
|
August 13, 2021
Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activation
Chiara Cavestro, Celeste Panteghini, Chiara Reale, et al.
Parkinsonism & Related Disorders
|
February 21, 2026
Early-onset parkinsonism with intellectual disability in an Italian family associated with a PTRHD1 variant
Giuseppe Pedullà, Maurizio Morelli, Paola Soliveri, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 30, 2022
Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome
Claudia M Bonardi, Allan Bayat, Camilla Gøbel Madsen, et al.
Parkinsonism & Related Disorders
|
October 2, 2022
ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcome
Giulia Straccia, Chiara Reale, Massimo Castellani, et al.
European Journal of Neurology
|
March 14, 2022
DNAJB2-related Charcot-Marie-Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening
Paola Saveri, Stefania Magri, Emanuela Maderna, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2016
DYT2 screening in early-onset isolated dystonia
Miryam Carecchio, Chiara Reale, Federica Invernizzi, et al.
Epilepsia
|
October 28, 2024
Quantitative EEG biomarkers for STXBP1-related disorders
Alberto Cossu, Francesca Furia, Jacopo Proietti, et al.
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of 5