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Frontiers in Neurology
|
October 29, 2020
Central Nervous System Involvement as Outcome Measure for Clinical Trials Efficacy in Myotonic Dystrophy Type 1
Costanza Simoncini, Giulia Spadoni, Elisa Lai, et al.
The Neurologist
|
November 2, 2012
Fabry disease with atypical neurological presentation: report of a case
Costanza Simoncini, Daniele Orsucci, Sara Gori, et al.
International Journal of Alzheimer'S Disease
|
March 23, 2011
May "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease?
Elena Caldarazzo Ienco, Costanza Simoncini, Daniele Orsucci, et al.
Mitochondrion
|
July 26, 2016
Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS
Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, et al.
Neuroimage. Clinical
|
July 21, 2016
Relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1
Sigrid Baldanzi, Paolo Cecchi, Serena Fabbri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 21, 2016
A multi-parametric protocol to study exercise intolerance in McArdle's disease
Giulia Ricci, Federica Bertolucci, Annalisa Logerfo, et al.
Neuromuscular Disorders : NMD
|
April 11, 2018
Disruption of sleep-wake continuum in myotonic dystrophy type 1: Beyond conventional sleep staging
Enrica Bonanni, Luca Carnicelli, Davide Crapanzano, et al.
Orphanet Journal of Rare Diseases
|
April 6, 2016
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
Sigrid Baldanzi, Francesca Bevilacqua, Rita Lorio, et al.
Medical & Biological Engineering & Computing
|
August 22, 2017
Towards a patient-specific hepatic arterial modeling for microspheres distribution optimization in SIRT protocol
Costanza Simoncini, Krzysztof Jurczuk, Daniel Reska, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 7, 2020
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
Patrizia Formichi, Nastasia Cardone, Ilaria Taglia, et al.
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Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Frontiers in Neurology
|
October 29, 2020
Central Nervous System Involvement as Outcome Measure for Clinical Trials Efficacy in Myotonic Dystrophy Type 1
Costanza Simoncini, Giulia Spadoni, Elisa Lai, et al.
The Neurologist
|
November 2, 2012
Fabry disease with atypical neurological presentation: report of a case
Costanza Simoncini, Daniele Orsucci, Sara Gori, et al.
International Journal of Alzheimer'S Disease
|
March 23, 2011
May "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease?
Elena Caldarazzo Ienco, Costanza Simoncini, Daniele Orsucci, et al.
Mitochondrion
|
July 26, 2016
Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS
Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, et al.
Neuroimage. Clinical
|
July 21, 2016
Relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1
Sigrid Baldanzi, Paolo Cecchi, Serena Fabbri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 21, 2016
A multi-parametric protocol to study exercise intolerance in McArdle's disease
Giulia Ricci, Federica Bertolucci, Annalisa Logerfo, et al.
Neuromuscular Disorders : NMD
|
April 11, 2018
Disruption of sleep-wake continuum in myotonic dystrophy type 1: Beyond conventional sleep staging
Enrica Bonanni, Luca Carnicelli, Davide Crapanzano, et al.
Orphanet Journal of Rare Diseases
|
April 6, 2016
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study
Sigrid Baldanzi, Francesca Bevilacqua, Rita Lorio, et al.
Medical & Biological Engineering & Computing
|
August 22, 2017
Towards a patient-specific hepatic arterial modeling for microspheres distribution optimization in SIRT protocol
Costanza Simoncini, Krzysztof Jurczuk, Daniel Reska, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 7, 2020
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
Patrizia Formichi, Nastasia Cardone, Ilaria Taglia, et al.
Page
of 3