Overview
Costanza Lamperti practices practicing medicine in Milan, Italy.
Lamperti is highly rated in 12 conditions, according to our data. Their clinical expertise encompasses Optic Nerve Atrophy, MELAS Syndrome, Progressive External Ophthalmoplegia, and Leber Hereditary Optic Neuropathy (LHON).
They are actively involved in clinical research, co-authoring 116 peer reviewed articles and participating in 1 clinical trial.
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.
1 Clinical Trials
Frequently Asked Questions about Costanza Lamperti
Is Costanza Lamperti a top-rated expert for Optic Nerve Atrophy?
MediFind is an objective health platform that identifies experts based on real-world data. Costanza Lamperti is classified as an Distinguished expert for Optic Nerve Atrophy, 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 Costanza Lamperti participate in research or clinical trials?
Yes. Costanza Lamperti has published 116 articles and abstracts on conditions like Optic Nerve Atrophy. You can view a list of Costanza Lamperti'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
- Leber Hereditary Optic Neuropathy (LHON)
- MELAS SyndromeLamperti isDistinguished. Learn about MELAS Syndrome.
- Optic Nerve AtrophyLamperti isDistinguished. Learn about Optic Nerve Atrophy.
- Progressive External OphthalmoplegiaLamperti isDistinguished. Learn about Progressive External Ophthalmoplegia.
- Advanced
- Alpers-Huttenlocher SyndromeLamperti isAdvanced. Learn about Alpers-Huttenlocher Syndrome.
- Drug Induced DyskinesiaLamperti isAdvanced. Learn about Drug Induced Dyskinesia.
- Lactic AcidosisLamperti isAdvanced. Learn about Lactic Acidosis.
- Leigh SyndromeLamperti isAdvanced. Learn about Leigh Syndrome.
- Mitochondrial Complex V Deficiency
- Myoclonic Epilepsy Associated With Ragged Red Fibers
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Experienced
- Absence SeizureLamperti isExperienced. Learn about Absence Seizure.
- Acute Cerebellar AtaxiaLamperti isExperienced. Learn about Acute Cerebellar Ataxia.
- Acute PainLamperti isExperienced. Learn about Acute Pain.
- AnhidrosisLamperti isExperienced. Learn about Anhidrosis.
- Beta-Propeller Protein-Associated Neurodegeneration
- Brown SyndromeLamperti isExperienced. Learn about Brown Syndrome.
- CACH SyndromeLamperti isExperienced. Learn about CACH Syndrome.
- CardiomyopathyLamperti isExperienced. Learn about Cardiomyopathy.
- Charcot-Marie-Tooth DiseaseLamperti isExperienced. Learn about Charcot-Marie-Tooth Disease.
- ChoreaLamperti isExperienced. Learn about Chorea.
- Cramp-Fasciculation SyndromeLamperti isExperienced. Learn about Cramp-Fasciculation Syndrome.
- Cytochrome C Oxidase DeficiencyLamperti isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Delayed GrowthLamperti isExperienced. Learn about Delayed Growth.
- Dentatorubral-Pallidoluysian Atrophy
- Dihydrolipoamide Dehydrogenase Deficiency
- DysarthriaLamperti isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic Encephalopathy
- EpilepsyLamperti isExperienced. Learn about Epilepsy.
- Epilepsy with Myoclonic-Atonic Seizures
- Familial HypopituitarismLamperti isExperienced. Learn about Familial Hypopituitarism.
- Familial Multiple LipomatosisLamperti isExperienced. Learn about Familial Multiple Lipomatosis.
- Generalized Tonic-Clonic SeizureLamperti isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Hajdu-Cheney SyndromeLamperti isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hallervorden-Spatz DiseaseLamperti isExperienced. Learn about Hallervorden-Spatz Disease.
- Hearing LossLamperti isExperienced. Learn about Hearing Loss.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- HypopituitarismLamperti isExperienced. Learn about Hypopituitarism.
- HypotoniaLamperti isExperienced. Learn about Hypotonia.
- Lafora DiseaseLamperti isExperienced. Learn about Lafora Disease.
- Late-Onset Retinal DegenerationLamperti isExperienced. Learn about Late-Onset Retinal Degeneration.
- LeukodystrophyLamperti isExperienced. Learn about Leukodystrophy.
- Metabolic AcidosisLamperti isExperienced. Learn about Metabolic Acidosis.
- Movement DisordersLamperti isExperienced. Learn about Movement Disorders.
- Multiple Symmetric LipomatosisLamperti isExperienced. Learn about Multiple Symmetric Lipomatosis.
- Myoclonic EpilepsyLamperti isExperienced. Learn about Myoclonic Epilepsy.
- Myoglobinuria RecurrentLamperti isExperienced. Learn about Myoglobinuria Recurrent.
- Palatal MyoclonusLamperti isExperienced. Learn about Palatal Myoclonus.
- PanhypopituitarismLamperti isExperienced. Learn about Panhypopituitarism.
- Pelizaeus-Merzbacher DiseaseLamperti isExperienced. Learn about Pelizaeus-Merzbacher Disease.
- Pompe DiseaseLamperti isExperienced. Learn about Pompe Disease.
- Renal Tubular AcidosisLamperti isExperienced. Learn about Renal Tubular Acidosis.
- RhabdomyolysisLamperti isExperienced. Learn about Rhabdomyolysis.
- SeizuresLamperti isExperienced. Learn about Seizures.
- Sheehan SyndromeLamperti isExperienced. Learn about Sheehan Syndrome.
- SpasticityLamperti isExperienced. Learn about Spasticity.
- Spinocerebellar Ataxia Type 28Lamperti isExperienced. Learn about Spinocerebellar Ataxia Type 28.
- Thymidine Kinase 2 Deficiency (TK2d)
- Tumefactive Multiple SclerosisLamperti isExperienced. Learn about Tumefactive Multiple Sclerosis.
- X-Linked Congenital Stationary Night Blindness