Overview
Giancarlo Parenti practices practicing medicine in Naples, Italy.
Mr. Parenti is highly rated in 15 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Pompe Disease, Von Gierke Disease, Mucopolysaccharidoses (MPS), and Hormone Replacement Therapy (HRT).
He is actively involved in clinical research, co-authoring 120 peer reviewed articles and participating in 2 clinical trials.
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.
2 Clinical Trials
Frequently Asked Questions about Giancarlo Parenti
Is Giancarlo Parenti a top-rated expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Giancarlo Parenti is classified as an Distinguished expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy 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 Giancarlo Parenti participate in research or clinical trials?
Yes. Giancarlo Parenti has published 120 articles and abstracts on conditions like Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). You can view a list of Giancarlo Parenti'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
- Distinguished
- Mucopolysaccharidoses (MPS)Mr. Parenti isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Pompe DiseaseMr. Parenti isDistinguished. Learn about Pompe Disease.
- Von Gierke DiseaseMr. Parenti isDistinguished. Learn about Von Gierke Disease.
- Advanced
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Cytochrome P450 Oxidoreductase Deficiency
- Glucose-6-Phosphate Translocase Deficiency
- Glycogen Storage Disease Type 3Mr. Parenti isAdvanced. Learn about Glycogen Storage Disease Type 3.
- HomocystinuriaMr. Parenti isAdvanced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR Deficiency
- Maternal HyperphenylalaninemiaMr. Parenti isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Multiple Sulfatase DeficiencyMr. Parenti isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Phenylketonuria (PKU)Mr. Parenti isAdvanced. Learn about Phenylketonuria (PKU).
- Phosphoglycerate Mutase DeficiencyMr. Parenti isAdvanced. Learn about Phosphoglycerate Mutase Deficiency.
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Mr. Parenti isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Ataxia-TelangiectasiaMr. Parenti isExperienced. Learn about Ataxia-Telangiectasia.
- Batten DiseaseMr. Parenti isExperienced. Learn about Batten Disease.
- Brachydactyly Mononen TypeMr. Parenti isExperienced. Learn about Brachydactyly Mononen Type.
- CardiomyopathyMr. Parenti isExperienced. Learn about Cardiomyopathy.
- Classic GalactosemiaMr. Parenti isExperienced. Learn about Classic Galactosemia.
- CLN1 DiseaseMr. Parenti isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMr. Parenti isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMr. Parenti isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMr. Parenti isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMr. Parenti isExperienced. Learn about CLN5 Disease.
- Congenital HyperinsulinismMr. Parenti isExperienced. Learn about Congenital Hyperinsulinism.
- Dihydrolipoamide Dehydrogenase DeficiencyMr. Parenti isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Fabry DiseaseMr. Parenti isExperienced. Learn about Fabry Disease.
- Fukuyama Type Muscular DystrophyMr. Parenti isExperienced. Learn about Fukuyama Type Muscular Dystrophy.
- Galactokinase DeficiencyMr. Parenti isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Parenti isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Parenti isExperienced. Learn about Galactosemia.
- Glutaric Acidemia Type 2Mr. Parenti isExperienced. Learn about Glutaric Acidemia Type 2.
- Hereditary Fructose IntoleranceMr. Parenti isExperienced. Learn about Hereditary Fructose Intolerance.
- High CholesterolMr. Parenti isExperienced. Learn about High Cholesterol.
- HistiocytosisMr. Parenti isExperienced. Learn about Histiocytosis.
- Hormone Replacement Therapy (HRT)Mr. Parenti isExperienced. Learn about Hormone Replacement Therapy (HRT).
- HypermethioninemiaMr. Parenti isExperienced. Learn about Hypermethioninemia.
- HypotoniaMr. Parenti isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaMr. Parenti isExperienced. Learn about Infantile Neutropenia.
- InfertilityMr. Parenti isExperienced. Learn about Infertility.
- LissencephalyMr. Parenti isExperienced. Learn about Lissencephaly.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Newborn Low Blood SugarMr. Parenti isExperienced. Learn about Newborn Low Blood Sugar.
- Niemann-Pick DiseaseMr. Parenti isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMr. Parenti isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Pyruvate Decarboxylase DeficiencyMr. Parenti isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Parenti isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- ReticulohistiocytomaMr. Parenti isExperienced. Learn about Reticulohistiocytoma.
- SpasticityMr. Parenti isExperienced. Learn about Spasticity.
- Stargardt Macular DegenerationMr. Parenti isExperienced. Learn about Stargardt Macular Degeneration.
- TelangiectasiaMr. Parenti isExperienced. Learn about Telangiectasia.
- Walker-Warburg SyndromeMr. Parenti isExperienced. Learn about Walker-Warburg Syndrome.
- Wiskott-Aldrich SyndromeMr. Parenti isExperienced. Learn about Wiskott-Aldrich Syndrome.
- X-Linked IchthyosisMr. Parenti isExperienced. Learn about X-Linked Ichthyosis.
- X-Linked Retinal DysplasiaMr. Parenti isExperienced. Learn about X-Linked Retinal Dysplasia.