Michelangelo Mancuso, Prof. Dr.
Rare Disease / Clinical Research
Università di Pisa
PI on 1 trial
ℹ
Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- Pyruvate metabolism disorder
- Coenzyme Q10 deficiency
- Hereditary vascular retinopathy
- Genetic central nervous system and retinal vascular disease
- MERRF
- Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
- NARP syndrome
- Ataxia-tapetoretinal degeneration syndrome
- Kearns-Sayre syndrome
- Muscle-eye-brain disease
- Mitochondrial myopathy
- Barth syndrome
- Ataxia neuropathy spectrum
- X-linked cerebellar ataxia
- Very long chain acyl-CoA dehydrogenase deficiency
- Progressive myoclonic epilepsy
- Progressive external ophthalmoplegia
- MELAS
- X-linked progressive cerebellar ataxia
Clinical trials (1)
Verify independently
Other specialists for Pyruvate metabolism disorder
Peers ranked by clinical-trial PI role, publications, and verification quality.
- Bruce Cohen, MDAkron Children's Hospital
- Jirair Bedoyan, MD, PhD, M.D.,Ph.DUPMC Children's Hospital of PittsburghPA
- Irene Litvan, MD, M.DUniversity of Louisville, Division of Movement DisordersKY
- Mary Kay Koenig, MDThe University of Texas Medical School at HoustonTexas
- Michio Hirano, MD, M.DColumbia UniversityNY
- Richard Neibeger, MDUniversity of FloridaCalifornia
- Petros Kountouris, PhDCyprus Institute of Neurology and Genetics (CING)
- Vinay Penematsa, MDPTC Therapeutics