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Education and qualifications (5)

Università degli Studi di Firenze: Firenze, Toscana, IT

MD (Facoltà di Medicina e Chirurgia)
Education
Source: Self-asserted source
Marinela Vavla

King's College London: London, London, GB

Master of Science in Neuroscience (Insitute of Psychiatry)
Education
Source: Self-asserted source
Marinela Vavla

Università degli Studi di Padova: Padova, Veneto, IT

2021-11-01 to 2025-10-31 | Specializzazione (Neuropsichiatria Infantile)
Education
Source: Self-asserted source
Marinela Vavla

Università degli Studi di Padova: Padova, Veneto, IT

2019-05 to 2020-05 | Post-doctoral Research
Education
Source: Self-asserted source
Marinela Vavla

Università degli Studi di Padova: Padova, Veneto, IT

2012-01 to 2015-03 | PhD in Medicina dello Sviluppo e Scienze della Programmazione (Salute della Donna e del Bambino)
Education
Source: Self-asserted source
Marinela Vavla

Works (19)

Brain Structure and Degeneration Staging in Friedreich Ataxia: MRI Volumetrics from the ENIGMA‐Ataxia Working Group

Annals of Neurology
2021-08-26 | Journal article
Part of ISSN: 0364-5134
Part of ISSN: 1531-8249
Source: Self-asserted source
Marinela Vavla

Trends observed in bilateral cerebral palsy during a thirty-year period: A cohort study with an ICF-based overview

Pediatrics & Neonatology
2021-02 | Journal article
Part of ISSN: 1875-9572
Source: Self-asserted source
Marinela Vavla

Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)

Orphanet Journal of Rare Diseases
2020-12 | Journal article
Part of ISSN: 1750-1172
Source: Self-asserted source
Marinela Vavla

Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

Genetics in Medicine
2020-12-22 | Journal article
Part of ISSN: 1098-3600
Part of ISSN: 1530-0366
Source: Self-asserted source
Marinela Vavla

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

Genetics in Medicine
2020-11 | Journal article
Part of ISSN: 1098-3600
Part of ISSN: 1530-0366
Source: Self-asserted source
Marinela Vavla

Sensitivity of Neuroimaging Indicators in Monitoring the Effects of Interferon Gamma Treatment in Friedreich’s Ataxia

Frontiers in Neuroscience
2020-10-09 | Journal article
Part of ISSN: 1662-453X
Source: Self-asserted source
Marinela Vavla

Brain Magnetic Spectroscopy Imaging and Hereditary Spastic Paraplegia: A Focused Systematic Review on Current Landmarks and Future Perspectives

Frontiers in Neurology
2020-07-14 | Journal article
Part of ISSN: 1664-2295
Source: Self-asserted source
Marinela Vavla

Safety and Efficacy Of Interferon γ in Friedreich's Ataxia

Movement Disorders
2020-02 | Journal article
Contributors: Marinela Vavla; Maria Grazia D'Angelo; Filippo Arrigoni; Nicola Toschi; Denis Peruzzo; Sandra Gandossini; Annamaria Russo; Eleonora Diella; Stefania Tirelli; Roberto Salati et al.
Source: check_circle
Crossref

Efficacy of a Combined Treatment of Botulinum Toxin and Intensive Physiotherapy in Hereditary Spastic Paraplegia

Frontiers in Neuroscience
2020-02-21 | Journal article
Part of ISSN: 1662-453X
Source: Self-asserted source
Marinela Vavla

Optical Coherence Tomography in a Cohort of Genetically Defined Hereditary Spastic Paraplegia: A Brief Research Report

Frontiers in Neurology
2019-11-22 | Journal article
Part of ISSN: 1664-2295
Source: Self-asserted source
Marinela Vavla

Functional and Structural Brain Damage in Friedreich's Ataxia

Frontiers in Neurology
2018-09-06 | Journal article
Part of ISSN: 1664-2295
Source: Self-asserted source
Marinela Vavla

Clinical and paraclinical indicators of motor system impairment in hereditary spastic paraplegia: A pilot study

PLoS ONE
2016 | Journal article
EID:

2-s2.0-84964380891

Contributors: Martinuzzi, A.; Montanaro, D.; Vavla, M.; Paparella, G.; Bonanni, P.; Musumeci, O.; Brighina, E.; Hlavata, H.; Rossi, G.; Aghakhanyan, G. et al.
Source: Self-asserted source
Marinela Vavla via Scopus - Elsevier

Extraocular phenotyping of mitochondrial optic neuropathy

Acta Ophthalmologica October 2015, Vol.93, pp.n/a-n/a
2015 | Journal article
Source: Self-asserted source
Marinela Vavla
grade
Preferred source (of 3)‎

ABS15‐0069 Extraocular phenotyping of mitochondrial optic neuropathy

Acta Ophthalmologica
2015-09-23 | Journal article
Source: Self-asserted source
Marinela Vavla

Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.

2014-08 | Journal article
Contributors: Aghakhanyan G; Martinuzzi A; Frijia F; Vavla M; Hlavata H; Baratto A; Martino N; Paparella G; Montanaro D
Source: Self-asserted source
Marinela Vavla via Europe PubMed Central
grade
Preferred source (of 2)‎

Whole brain-based analysis of grey matter alteration pattern in hereditary spastic paraparesis with SPG11 mutation: 182

Movement Disorders
2014-05-01 | Journal article
Source: Self-asserted source
Marinela Vavla

The use of telemonitoring and illustrated handbook to assess Parkinson's disease patients' adherence to home-prescribed physiotherapy treatment: PP2215

European Journal of Neurology. 21():537
2014-05-01 | Journal article
Source: Self-asserted source
Marinela Vavla
grade
Preferred source (of 2)‎

A novel mitofusin 2 MFN2 gene mutation causing early onset Charcot-Marie-Tooth 2A disease: Genetic, clinical and MR spectroscopy characterization

JOURNAL OF THE NEUROLOGICAL SCIENCES
2013 | Journal article
Source: Self-asserted source
Marinela Vavla

POD09 Using the chick embryo model system to study the neurotoxicity of TDP43

Journal of Neurology, Neurosurgery & Psychiatry
2010-11-01 | Journal article
Source: Self-asserted source
Marinela Vavla