alessandro filla

About alessandro filla

alessandro filla, With an exceptional h-index of 71 and a recent h-index of 43 (since 2020), a distinguished researcher at Università degli Studi di Napoli Federico II, specializes in the field of Neurology.

His recent articles reflect a diverse array of research interests and contributions to the field:

Spectral Domain and Angiography Optical Coherence Tomography in Parkinson’s Disease: Structural And Vascular Changes in the Retina Correlate with Disease Severity and Progression

Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System Atrophy

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice

Genome-wide association study identifies a new susceptibility locus inPLA2G4Cfor Multiple System Atrophy

Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult‐Onset Degenerative Ataxia

Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes

A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A

alessandro filla Information

University

Position

___

Citations(all)

24285

Citations(since 2020)

7451

Cited By

20099

hIndex(all)

71

hIndex(since 2020)

43

i10Index(all)

238

i10Index(since 2020)

139

Email

University Profile Page

Google Scholar

alessandro filla Skills & Research Interests

Neurology

Top articles of alessandro filla

Spectral Domain and Angiography Optical Coherence Tomography in Parkinson’s Disease: Structural And Vascular Changes in the Retina Correlate with Disease Severity and Progression

Acta Neurologica Scandinavica

2024/4/15

Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice

2023/7

Alessandro Filla
Alessandro Filla

H-Index: 37

Genome-wide association study identifies a new susceptibility locus inPLA2G4Cfor Multiple System Atrophy

2023/5/3

Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult‐Onset Degenerative Ataxia

Movement Disorders

2023/4

Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes

2023/3/30

Sirio Cocozza
Sirio Cocozza

H-Index: 17

Alessandro Filla
Alessandro Filla

H-Index: 37

A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A

Journal of Neurology

2023/10

Sirio Cocozza
Sirio Cocozza

H-Index: 17

Alessandro Filla
Alessandro Filla

H-Index: 37

The organizational dimension in rare diseases care management: an application of RarERN Path© methodology in the rare neurological diseases Ataxia, Dystonia and Phenylketonuria

2023/8/24

POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients

Neurological Sciences

2022/2/1

Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia

European Journal of Preventive Cardiology

2022/2/1

Alessandro Filla
Alessandro Filla

H-Index: 37

Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosis

Journal of Neurology

2022/10

Alessandro Filla
Alessandro Filla

H-Index: 37

How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey

European journal of neurology

2022/7

Alessandro Filla
Alessandro Filla

H-Index: 37

Levels of neurofilament light at the preataxic and ataxic stages of spinocerebellar ataxia type 1

Neurology

2022/5/17

Alessandro Filla
Alessandro Filla

H-Index: 37

Clinical-genetic features influencing disability in spastic paraplegia type 4: a cross-sectional study by the Italian DAISY network

Neurology: Genetics

2022/3/30

Sensory axonal neuropathy in RFC1-disease: tip of the iceberg of broad subclinical multisystemic neurodegeneration

Brain

2022/3/1

Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations

Journal of Neurology

2022/3/1

Clinical and genetic features of a large cohort of Italian SPG4 patients from the DAISY collaborative network

Journal of the Neurological Sciences

2021/10/1

Serum NfL in spinocerebellar ataxia type 1 is increased already at the preataxic stage, correlating with proximity to clinical onset

medRxiv

2021/9/22

Alessandro Filla
Alessandro Filla

H-Index: 37

NGS in hereditary ataxia: when rare becomes frequent

International Journal of Molecular Sciences

2021/8/6

See List of Professors in alessandro filla University(Università degli Studi di Napoli Federico II)