Barbara Borroni, MD

Rare Disease / Clinical Research

Azienda Ospedaliera Spedali Civili, Brescia

PI on 7 trials

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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.

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Rare diseases treated or studied

Based on trial PI assignments and publication topics.

Primary progressive aphasia
Amyotrophic lateral sclerosis
Autosomal recessive metabolic cerebellar ataxia
Friedreich ataxia
Cogan syndrome
Semantic dementia
Ataxia-oculomotor apraxia type 1
Multiple system atrophy, cerebellar type
Frontotemporal dementia
Autosomal recessive congenital cerebellar ataxia
Spinocerebellar ataxia with axonal neuropathy type 2
Machado-Joseph disease type 3
CLN11 disease
Primary progressive apraxia of speech
Autosomal recessive cerebral atrophy
Machado-Joseph disease type 2
Machado-Joseph disease type 1
Spinocerebellar ataxia type 38
Autosomal recessive cerebellar ataxia

Clinical trials (7)

NCT03109626
NCT04153110
NCT02999282
NCT03120013
NCT05621200
NCT04293484
NCT03293394

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ClinicalTrials.gov PI search for Barbara Borroni, MD

Other specialists for Primary progressive aphasia

Peers ranked by clinical-trial PI role, publications, and verification quality.

Alberto Benussi, MD
Università degli Studi di Brescia
Trieste
Forbes D Porter, M.D.
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Maryland
Mitchell S Cairo, MD, MD
New York Medical College
NY
Darby Morhardt, PhD, MSW, LCSW
Northwestern University
IL
Jennifer Whitwell, PhD
Mayo Clinic
Justin Y Kwan, M.D., O.D
National Institute of Neurological Disorders and Stroke (NINDS)
IL
Doreen Görß, MD
Rostock University Medical Center
Maria C Tartaglia, M.D.
Toronto Western Hospital, UHN; Tanz CRND

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