Overview
Maria Chondrogianni practices practicing medicine in Athens, Greece.
Her clinical expertise encompasses Familial Hypocalciuric Hypercalcemia Type 1, Autosomal Dominant Hypocalcemia, Bartter Syndrome, and Osteoporosis.
She is actively involved in clinical research, co-authoring 9 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 Maria E. Chondrogianni
Is Maria E. Chondrogianni a top-rated expert for Familial Hypocalciuric Hypercalcemia Type 1?
MediFind is an objective health platform that identifies experts based on real-world data. Maria E. Chondrogianni is classified as an Experienced expert for Familial Hypocalciuric Hypercalcemia Type 1, 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 Maria E. Chondrogianni participate in research or clinical trials?
Yes. Maria E. Chondrogianni has published 9 articles and abstracts on conditions like Familial Hypocalciuric Hypercalcemia Type 1. You can view a list of Maria E. Chondrogianni'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
- Experienced
- Autosomal Dominant HypocalcemiaMs. Chondrogianni isExperienced. Learn about Autosomal Dominant Hypocalcemia.
- Bartter SyndromeMs. Chondrogianni isExperienced. Learn about Bartter Syndrome.
- Beckwith-Wiedemann SyndromeMs. Chondrogianni isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Chronic Myelogenous Leukemia (CML)Ms. Chondrogianni isExperienced. Learn about Chronic Myelogenous Leukemia (CML).
- Familial Hypocalciuric Hypercalcemia Type 1Ms. Chondrogianni isExperienced. Learn about Familial Hypocalciuric Hypercalcemia Type 1.
- Gestational Trophoblastic DiseaseMs. Chondrogianni isExperienced. Learn about Gestational Trophoblastic Disease.
- Hydatidiform MoleMs. Chondrogianni isExperienced. Learn about Hydatidiform Mole.
- HyperaldosteronismMs. Chondrogianni isExperienced. Learn about Hyperaldosteronism.
- HypercalcemiaMs. Chondrogianni isExperienced. Learn about Hypercalcemia.
- HypoparathyroidismMs. Chondrogianni isExperienced. Learn about Hypoparathyroidism.
- Magnesium DeficiencyMs. Chondrogianni isExperienced. Learn about Magnesium Deficiency.
- Milk-Alkali SyndromeMs. Chondrogianni isExperienced. Learn about Milk-Alkali Syndrome.
- Non-Alcoholic Fatty Liver DiseaseMs. Chondrogianni isExperienced. Learn about Non-Alcoholic Fatty Liver Disease.
- OsteoporosisMs. Chondrogianni isExperienced. Learn about Osteoporosis.
- Postmenopausal OsteoporosisMs. Chondrogianni isExperienced. Learn about Postmenopausal Osteoporosis.