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Christian Marcotulli

Observed names: C. Marcotulli, MARCOTULLI, CHRISTIAN, Marcotulli C
ORCID: 0000-0002-5862-804X
Observed ORCID: 0000-0002-5862-804X
OpenAlex ID: A5060209585
Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial
2015 · Silvia Romano, Giulia Coarelli, et al. · The Lancet Neurology · 216
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
2018 · Angelica D'Amore, Alessandra Tessa, et al. · Frontiers in Neurology · 89
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Identification of specific gait patterns in patients with cerebellar ataxia, spastic paraplegia, and Parkinson’s disease: A non-hierarchical cluster analysis
2017 · Mariano Serrao, Giorgia Chini, et al. · Human Movement Science · 55
Progression of Gait Ataxia in Patients with Degenerative Cerebellar Disorders: a 4-Year Follow-Up Study
2016 · Mariano Serrao, Giorgia Chini, et al. · The Cerebellum · 48
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family
2016 · Luca Leonardi, Lucia Ziccardi, et al. · Journal of Neurology · 37
A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study
2016 · Luca Leonardi, Maria Gabriella Aceto, et al. · Neurological Sciences · 35
L ong‐term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia
2016 · Francesco Saccà, Giorgia Puorro, et al. · Movement Disorders · 32
Developing a smartphone application, triaxial accelerometer-based, to quantify static and dynamic balance deficits in patients with cerebellar ataxias
2019 · Giuseppe Arcuria, Christian Marcotulli, et al. · Journal of Neurology · 31
Cortical sources of resting state electroencephalographic rhythms differ in relapsing–remitting and secondary progressive multiple sclerosis
2015 · Claudio Babiloni, Claudio Del Percio, et al. · Clinical Neurophysiology · 31
Cerebellum and neuropsychiatric disorders: insights from ARSACS
2013 · Andrea Mignarri, Alessandra Tessa, et al. · Neurological Sciences · 29
GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients
2015 · Christian Marcotulli, Silvia Fortuni, et al. · Neurological Sciences · 27
Acute optic neuropathy associated with a novel MFN2 mutation
2015 · Luca Leonardi, Christian Marcotulli, et al. · Journal of Neurology · 21
Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease
2014 · Luca Leonardi, Christian Marcotulli, et al. · Journal of Neurology · 21
15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias
2019 · Giuseppe Arcuria, Christian Marcotulli, et al. · Journal of Neurology · 18
Dataset on gait patterns in degenerative neurological diseases
2017 · Mariano Serrao, Giorgia Chini, et al. · Data in Brief · 18
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Early-onset optic neuropathy as initial clinical presentation in SPG7
2014 · Christian Marcotulli, Luca Leonardi, et al. · Journal of Neurology · 18
The Working Life of People with Degenerative Cerebellar Ataxia
2019 · A. Ranavolo, M. Serrao, et al. · The Cerebellum · 13
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival
2020 · Francesca Tiano, Francesca Amati, et al. · Human Molecular Genetics · 11
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Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia
2020 · Chiara Pane, Andrea Salzano, et al. · European Journal of Preventive Cardiology · 10
De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling
2015 · Luca Leonardi, Christian Marcotulli, et al. · Neurological Sciences · 8
Hsa-miR223-3p circulating level is upregulated in Friedreich’s ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1
2022 · Andrea Quatrana, Elena Morini, et al. · Human Molecular Genetics · 6
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‘When atlastin meets spastin’
2014 · R. Di Fabio, A. Tessa, et al. · Clinical Genetics · 6
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1
2014 · Roberto Di Fabio, Christian Marcotulli, et al. · Journal of Neurology · 5
Developing an objective evaluating system to quantify the degree of upper limb movement impairment in patients with severe Friedreich’s ataxia
2020 · Giuseppe Arcuria, Christian Marcotulli, et al. · Neurological Sciences · 4
Retinal and Visual Pathways Involvement in Carriers of Friedreich’s Ataxia
2022 · Lucia Ziccardi, Lucilla Barbano, et al. · Diagnostics · 3
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Works count: 33
Citation count: 794
H-index: 16
I10-index: 19
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