Overview
Elisa Piscianz practices practicing medicine in Trieste, Italy.
Ms. Piscianz is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Mevalonate Kinase Deficiency, Smith-Lemli-Opitz Syndrome, Familial Glucocorticoid Deficiency, and Cowden Syndrome.
She is actively involved in clinical research, co-authoring 45 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 Elisa Piscianz
Is Elisa Piscianz a top-rated expert for Mevalonate Kinase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Elisa Piscianz is classified as an Distinguished expert for Mevalonate Kinase Deficiency, 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 Elisa Piscianz participate in research or clinical trials?
Yes. Elisa Piscianz has published 45 articles and abstracts on conditions like Mevalonate Kinase Deficiency. You can view a list of Elisa Piscianz'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
- Mevalonate Kinase DeficiencyMs. Piscianz isDistinguished. Learn about Mevalonate Kinase Deficiency.
- Experienced
- Aicardi-Goutieres SyndromeMs. Piscianz isExperienced. Learn about Aicardi-Goutieres Syndrome.
- Bannayan-Riley-Ruvalcaba SyndromeMs. Piscianz isExperienced. Learn about Bannayan-Riley-Ruvalcaba Syndrome.
- Common Variable Immune DeficiencyMs. Piscianz isExperienced. Learn about Common Variable Immune Deficiency.
- Cowden SyndromeMs. Piscianz isExperienced. Learn about Cowden Syndrome.
- Familial Glucocorticoid DeficiencyMs. Piscianz isExperienced. Learn about Familial Glucocorticoid Deficiency.
- Lhermitte-Duclos DiseaseMs. Piscianz isExperienced. Learn about Lhermitte-Duclos Disease.
- Membranoproliferative GlomerulonephritisMs. Piscianz isExperienced. Learn about Membranoproliferative Glomerulonephritis.
- Niemann-Pick DiseaseMs. Piscianz isExperienced. Learn about Niemann-Pick Disease.
- Pediatric MyocarditisMs. Piscianz isExperienced. Learn about Pediatric Myocarditis.
- RASopathiesMs. Piscianz isExperienced. Learn about RASopathies.
- Smith-Lemli-Opitz SyndromeMs. Piscianz isExperienced. Learn about Smith-Lemli-Opitz Syndrome.
- Systemic Lupus Erythematosus (SLE)Ms. Piscianz isExperienced. Learn about Systemic Lupus Erythematosus (SLE).