Overview
Giancarlo La Marca practices practicing medicine in Florence, Italy.
Mr. La Marca is highly rated in 13 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Purine Nucleoside Phosphorylase Deficiency, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
He is actively involved in clinical research, co-authoring 133 peer reviewed articles.
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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 Giancarlo La Marca
Is Giancarlo La Marca a top-rated expert for Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Giancarlo La Marca is classified as an Elite expert for Mucopolysaccharidosis Type 1 (MPS I, Hurler 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 La Marca participate in research or clinical trials?
Yes. Giancarlo La Marca has published 133 articles and abstracts on conditions like Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). You can view a list of Giancarlo La Marca'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
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Distinguished
- Mucopolysaccharidoses (MPS)Mr. La Marca isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Purine Nucleoside Phosphorylase DeficiencyMr. La Marca isDistinguished. Learn about Purine Nucleoside Phosphorylase Deficiency.
- Severe Combined Immunodeficiency (SCID)Mr. La Marca isDistinguished. Learn about Severe Combined Immunodeficiency (SCID).
- Advanced
- Argininosuccinic AciduriaMr. La Marca isAdvanced. Learn about Argininosuccinic Aciduria.
- Biotinidase DeficiencyMr. La Marca isAdvanced. Learn about Biotinidase Deficiency.
- Homocystinuria due to MTHFR Deficiency
- Isovaleric AcidemiaMr. La Marca isAdvanced. Learn about Isovaleric Acidemia.
- Multiple Carboxylase DeficiencyMr. La Marca isAdvanced. Learn about Multiple Carboxylase Deficiency.
- Pompe DiseaseMr. La Marca isAdvanced. Learn about Pompe Disease.
- Urea Cycle Disorders (UCD)Mr. La Marca isAdvanced. Learn about Urea Cycle Disorders (UCD).
- West SyndromeMr. La Marca isAdvanced. Learn about West Syndrome.
- Experienced
- Adenosine Deaminase DeficiencyMr. La Marca isExperienced. Learn about Adenosine Deaminase Deficiency.
- Alpha MannosidosisMr. La Marca isExperienced. Learn about Alpha Mannosidosis.
- Atrial TachycardiaMr. La Marca isExperienced. Learn about Atrial Tachycardia.
- Brachydactyly Mononen TypeMr. La Marca isExperienced. Learn about Brachydactyly Mononen Type.
- CACH SyndromeMr. La Marca isExperienced. Learn about CACH Syndrome.
- CitrullinemiaMr. La Marca isExperienced. Learn about Citrullinemia.
- Congenital Central Hypoventilation SyndromeMr. La Marca isExperienced. Learn about Congenital Central Hypoventilation Syndrome.
- Cystic FibrosisMr. La Marca isExperienced. Learn about Cystic Fibrosis.
- DehydrationMr. La Marca isExperienced. Learn about Dehydration.
- Dihydrolipoamide Dehydrogenase DeficiencyMr. La Marca isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- EpilepsyMr. La Marca isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenMr. La Marca isExperienced. Learn about Epilepsy in Children.
- Fabry DiseaseMr. La Marca isExperienced. Learn about Fabry Disease.
- GangliosidosisMr. La Marca isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMr. La Marca isExperienced. Learn about GM1 Gangliosidosis.
- HomocystinuriaMr. La Marca isExperienced. Learn about Homocystinuria.
- Infantile ApneaMr. La Marca isExperienced. Learn about Infantile Apnea.
- Krabbe DiseaseMr. La Marca isExperienced. Learn about Krabbe Disease.
- LeukodystrophyMr. La Marca isExperienced. Learn about Leukodystrophy.
- Lysinuric Protein IntoleranceMr. La Marca isExperienced. Learn about Lysinuric Protein Intolerance.
- Maternal HyperphenylalaninemiaMr. La Marca isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Metachromatic LeukodystrophyMr. La Marca isExperienced. Learn about Metachromatic Leukodystrophy.
- Methylmalonic AcidemiaMr. La Marca isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- N-Acetylglutamate Synthase DeficiencyMr. La Marca isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Patent Ductus ArteriosusMr. La Marca isExperienced. Learn about Patent Ductus Arteriosus.
- Phenylketonuria (PKU)Mr. La Marca isExperienced. Learn about Phenylketonuria (PKU).
- Premature InfantMr. La Marca isExperienced. Learn about Premature Infant.
- Primary Immunodeficiency (PID)Mr. La Marca isExperienced. Learn about Primary Immunodeficiency (PID).
- Primary Lateral SclerosisMr. La Marca isExperienced. Learn about Primary Lateral Sclerosis.
- Retinopathy of PrematurityMr. La Marca isExperienced. Learn about Retinopathy of Prematurity.
- Spasmus NutansMr. La Marca isExperienced. Learn about Spasmus Nutans.
- SpasticityMr. La Marca isExperienced. Learn about Spasticity.
- Sudden Infant Death Syndrome (SIDS)Mr. La Marca isExperienced. Learn about Sudden Infant Death Syndrome (SIDS).
- Tyrosinemia Type 1Mr. La Marca isExperienced. Learn about Tyrosinemia Type 1.
- Vitamin B12 Deficiency AnemiaMr. La Marca isExperienced. Learn about Vitamin B12 Deficiency Anemia.