• 1370 Citations
  • 18 h-Index
1988 …2019
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Fingerprint Dive into the research topics where Stefania Bianchi Marzoli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 13 Similar Profiles
Leber's Hereditary Optic Atrophy Medicine & Life Sciences
Optic Nerve Medicine & Life Sciences
Pseudotumor Cerebri Medicine & Life Sciences
Oculomotor Muscles Medicine & Life Sciences
Autosomal Dominant Optic Atrophy Medicine & Life Sciences
Optic Neuritis Medicine & Life Sciences
Optic Nerve Diseases Medicine & Life Sciences
Meningioma Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1988 2019

  • 1370 Citations
  • 18 h-Index
  • 73 Article
  • 1 Review article
2 Citations (Scopus)

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results

on behalf of GEN-O-MA study group, Jan 1 2019, (Accepted/In press) In : Neurological Sciences.

Research output: Contribution to journalArticle

Age of Onset
Neuroimaging
Italy
Phenotype
Disease Susceptibility
2 Citations (Scopus)
1 Citation (Scopus)

Optical coherence tomography is a useful tool in the differentiation between true edema and pseudoedema of the optic disc

Carta, A., Mora, P., Aldigeri, R., Gozzi, F., Favilla, S., Tedesco, S., Calzetti, G., Farci, R., Barboni, P., Bianchi-Marzoli, S., Fossarello, M., Gandolfi, S. & Sadun, A. A., Nov 1 2018, In : PLoS One. 13, 11, e0208145.

Research output: Contribution to journalArticle

Papilledema
Optical tomography
tomography
Optical Coherence Tomography
optics
2 Citations (Scopus)

Pain in optic neuropathies

Marzoli, S. B. & Criscuoli, A., Jun 1 2018, In : Neurological Sciences. 39, p. 25-31 7 p.

Research output: Contribution to journalReview article

Optic Nerve Diseases
Giant Cell Arteritis
Scleritis
Pseudotumor Cerebri
Pain

Retinal dysfunction characterizes subtypes of dominant optic atrophy

Cascavilla, M. L., Parisi, V., Triolo, G., Ziccardi, L., Borrelli, E., Di Renzo, A., Balducci, N., Lamperti, C., Bianchi Marzoli, S., Darvizeh, F., Sadun, A. A., Carelli, V., Bandello, F. & Barboni, P., 2018, In : Acta Ophthalmologica. 96, 2, p. e156-e163

Research output: Contribution to journalArticle

Autosomal Dominant Optic Atrophy
Mutation
Haploinsufficiency
Missense Mutation
Nose