Overview
Corrado Angelini practices in Padova, Italy. Mr. Angelini and is rated as an Elite expert by MediFind in the treatment of Pompe Disease. His top areas of expertise are Limb-Girdle Muscular Dystrophy, Myotonic Dystrophy, Myotonic Dystrophy Type 2, and Paramyotonia Congenita.
His clinical research consists of co-authoring 225 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 30 articles in the study of Pompe Disease.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Glutaric Acidemia Type 2Mr. Angelini isElite. Learn about Glutaric Acidemia Type 2.
- Limb-Girdle Muscular DystrophyMr. Angelini isElite. Learn about Limb-Girdle Muscular Dystrophy.
- Myotonic DystrophyMr. Angelini isElite. Learn about Myotonic Dystrophy.
- Myotonic Dystrophy Type 2Mr. Angelini isElite. Learn about Myotonic Dystrophy Type 2.
- Paramyotonia CongenitaMr. Angelini isElite. Learn about Paramyotonia Congenita.
- Distinguished
- Becker Muscular DystrophyMr. Angelini isDistinguished. Learn about Becker Muscular Dystrophy.
- Carnitine Palmitoyltransferase 1 DeficiencyMr. Angelini isDistinguished. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyMr. Angelini isDistinguished. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Chanarin-Dorfman SyndromeMr. Angelini isDistinguished. Learn about Chanarin-Dorfman Syndrome.
- Duchenne Muscular DystrophyMr. Angelini isDistinguished. Learn about Duchenne Muscular Dystrophy.
- DysferlinopathyMr. Angelini isDistinguished. Learn about Dysferlinopathy.
- Advanced
- Adult Polyglucosan Body DiseaseMr. Angelini isAdvanced. Learn about Adult Polyglucosan Body Disease.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- CardiomyopathyMr. Angelini isAdvanced. Learn about Cardiomyopathy.
- Cerebral HypoxiaMr. Angelini isAdvanced. Learn about Cerebral Hypoxia.
- Danon DiseaseMr. Angelini isAdvanced. Learn about Danon Disease.
- Delta-SarcoglycanopathyMr. Angelini isAdvanced. Learn about Delta-Sarcoglycanopathy.
- Experienced
- Acute Cerebellar AtaxiaMr. Angelini isExperienced. Learn about Acute Cerebellar Ataxia.
- AgnosiaMr. Angelini isExperienced. Learn about Agnosia.
- Alternating Hemiplegia of ChildhoodMr. Angelini isExperienced. Learn about Alternating Hemiplegia of Childhood.
- Amyotonia CongenitaMr. Angelini isExperienced. Learn about Amyotonia Congenita.
- Andersen DiseaseMr. Angelini isExperienced. Learn about Andersen Disease.
- Benign Autosomal Dominant MyopathyMr. Angelini isExperienced. Learn about Benign Autosomal Dominant Myopathy.