Overview
Amelia Morrone practices practicing medicine in Florence, Italy.
Ms. Morrone is highly rated in 16 conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Brachydactyly Mononen Type, Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), and PMM2-Congenital Disorder of Glycosylation.
She is actively involved in clinical research, co-authoring 104 peer reviewed articles.
Gender
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.
Frequently Asked Questions about Amelia Morrone
Is Amelia Morrone a top-rated expert for Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Amelia Morrone is classified as an Elite expert for Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Amelia Morrone participate in research or clinical trials?
Yes. Amelia Morrone has published 104 articles and abstracts on conditions like Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome). You can view a list of Amelia Morrone's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Brachydactyly Mononen TypeMs. Morrone isElite. Learn about Brachydactyly Mononen Type.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- Distinguished
- Farber LipogranulomatosisMs. Morrone isDistinguished. Learn about Farber Lipogranulomatosis.
- GangliosidosisMs. Morrone isDistinguished. Learn about Gangliosidosis.
- Gaucher DiseaseMs. Morrone isDistinguished. Learn about Gaucher Disease.
- GM1 GangliosidosisMs. Morrone isDistinguished. Learn about GM1 Gangliosidosis.
- Mucopolysaccharidoses (MPS)Ms. Morrone isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- PMM2-Congenital Disorder of GlycosylationMs. Morrone isDistinguished. Learn about PMM2-Congenital Disorder of Glycosylation.
- Advanced
- Biotinidase DeficiencyMs. Morrone isAdvanced. Learn about Biotinidase Deficiency.
- Fabry DiseaseMs. Morrone isAdvanced. Learn about Fabry Disease.
- Mucolipidosis 3Ms. Morrone isAdvanced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Morrone isAdvanced. Learn about Mucolipidosis Type 4.
- Multiple Carboxylase DeficiencyMs. Morrone isAdvanced. Learn about Multiple Carboxylase Deficiency.
- Multiple Sulfatase DeficiencyMs. Morrone isAdvanced. Learn about Multiple Sulfatase Deficiency.
- SialidosisMs. Morrone isAdvanced. Learn about Sialidosis.
- Experienced
- Barth SyndromeMs. Morrone isExperienced. Learn about Barth Syndrome.
- Batten DiseaseMs. Morrone isExperienced. Learn about Batten Disease.
- CACH SyndromeMs. Morrone isExperienced. Learn about CACH Syndrome.
- CardiomyopathyMs. Morrone isExperienced. Learn about Cardiomyopathy.
- Central Sleep ApneaMs. Morrone isExperienced. Learn about Central Sleep Apnea.
- Cerebrotendinous XanthomatosisMs. Morrone isExperienced. Learn about Cerebrotendinous Xanthomatosis.
- CholestasisMs. Morrone isExperienced. Learn about Cholestasis.
- CLN1 DiseaseMs. Morrone isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Morrone isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Morrone isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Morrone isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Morrone isExperienced. Learn about CLN5 Disease.
- Congenital Central Hypoventilation Syndrome
- Cortical DysplasiaMs. Morrone isExperienced. Learn about Cortical Dysplasia.
- Delayed GrowthMs. Morrone isExperienced. Learn about Delayed Growth.
- Dentatorubral-Pallidoluysian AtrophyMs. Morrone isExperienced. Learn about Dentatorubral-Pallidoluysian Atrophy.
- Developmental Expressive Language Disorder
- Dilated Cardiomyopathy (DCM)Ms. Morrone isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Drug Induced DyskinesiaMs. Morrone isExperienced. Learn about Drug Induced Dyskinesia.
- HemochromatosisMs. Morrone isExperienced. Learn about Hemochromatosis.
- Hepatocerebral DegenerationMs. Morrone isExperienced. Learn about Hepatocerebral Degeneration.
- High Blood Pressure in InfantsMs. Morrone isExperienced. Learn about High Blood Pressure in Infants.
- HomocystinuriaMs. Morrone isExperienced. Learn about Homocystinuria.
- Hypertrophic Cardiomyopathy (HCM)Ms. Morrone isExperienced. Learn about Hypertrophic Cardiomyopathy (HCM).
- Infantile NeutropeniaMs. Morrone isExperienced. Learn about Infantile Neutropenia.
- IntersexMs. Morrone isExperienced. Learn about Intersex.
- JaundiceMs. Morrone isExperienced. Learn about Jaundice.
- Krabbe DiseaseMs. Morrone isExperienced. Learn about Krabbe Disease.
- Lactic AcidosisMs. Morrone isExperienced. Learn about Lactic Acidosis.
- Lafora DiseaseMs. Morrone isExperienced. Learn about Lafora Disease.
- LeukodystrophyMs. Morrone isExperienced. Learn about Leukodystrophy.
- Liver FailureMs. Morrone isExperienced. Learn about Liver Failure.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- MELAS SyndromeMs. Morrone isExperienced. Learn about MELAS Syndrome.
- Metachromatic LeukodystrophyMs. Morrone isExperienced. Learn about Metachromatic Leukodystrophy.
- Movement DisordersMs. Morrone isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- N-Acetylglutamate Synthase DeficiencyMs. Morrone isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Niemann-Pick DiseaseMs. Morrone isExperienced. Learn about Niemann-Pick Disease.
- Palatal MyoclonusMs. Morrone isExperienced. Learn about Palatal Myoclonus.
- Parkinson's DiseaseMs. Morrone isExperienced. Learn about Parkinson's Disease.
- Pompe DiseaseMs. Morrone isExperienced. Learn about Pompe Disease.
- Propionic AcidemiaMs. Morrone isExperienced. Learn about Propionic Acidemia.
- Short Stature (Growth Disorders)Ms. Morrone isExperienced. Learn about Short Stature (Growth Disorders).
- Tay-Sachs DiseaseMs. Morrone isExperienced. Learn about Tay-Sachs Disease.
- Transient Ischemic Attack (TIA)Ms. Morrone isExperienced. Learn about Transient Ischemic Attack (TIA).
- Urea Cycle Disorders (UCD)Ms. Morrone isExperienced. Learn about Urea Cycle Disorders (UCD).
- Wilson DiseaseMs. Morrone isExperienced. Learn about Wilson Disease.
- XanthomaMs. Morrone isExperienced. Learn about Xanthoma.