Concepedia

Author

Marcella Masciullo

Fondazione Santa LuciaORCID

Also Known As

Jon Infante, M. Masciullo, Marcella Masciullo, Marcella Masciullo (578456), Masciullo Marcella, Masciullo, Marcella

106

Publications

2.7K

Citations

32

H-Index

120

Concepts

All Affiliations

Fondazione Santa LuciaDon Carlo Gnocchi FoundationUniversità Cattolica del Sacro CuoreIstituti di Ricovero e Cura a Carattere ScientificoSapienza University of Rome
MM

About

Marcella Masciullo is an author at Fondazione Santa Lucia specializing in medicine, neurology, and neuroscience.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

21

27

1.1K

2

Social Sciences

8

8

262

3

Health Sciences

5

5

234

4

Public Health

2

2

97

5

Applied Physiology

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Marcella Masciullo

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46

Publications

2.1K

Citations

31

H-Index

YearCitations

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

Heike Jacobi, Kathrin Reetz, Sophie Tézenas du Montcel,

The Lancet Neurology

2013

188

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

Sophie Tézenas du Montcel, Alexandra Dürr, Maria Rakowicz,

Journal of Medical Genetics

2014

117

Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice

Carlo Wilke, Eva Haas, Kathrin Reetz,

EMBO Molecular Medicine

2020

97

Symbitron Exoskeleton: Design, Control, and Evaluation of a Modular Exoskeleton for Incomplete and Complete Spinal Cord Injured Individuals

C. Meijneke, Gijs van Oort, Victor Sluiter,

IEEE Transactions on Neural Systems and Rehabilitation Engineering

2021

97

Muscle MRI in Becker muscular dystrophy

Giorgio Tasca, Elisabetta Iannaccone, Mauro Monforte,

Neuromuscular Disorders

2012

87

Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy

Giorgio Tasca, Mauro Monforte, Elisabetta Iannaccone,

PLoS ONE

2014

87

Abnormal Functional Brain Connectivity and Personality Traits in Myotonic Dystrophy Type 1

Laura Serra, Gabriella Silvestri, Antonio Petrucci,

JAMA Neurology

2014

69

Screening of ARHSP-TCC patients expands the spectrum of<i>SPG11</i>mutations and includes a large scale gene deletion

Paola S. Denora, David Schlesinger, Carlo Casali,

Human Mutation

2008

59

Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia

Ilaria Giordano, Florian Harmuth, Heike Jacobi,

Neurology

2017

58

Prevalence and clinical correlates of sleep disordered breathing in myotonic dystrophy types 1 and 2

Maria Laura Ester Bianchi, Anna Losurdo, Chiara Di Blasi,

Sleep And Breathing

2013

57

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