Overview
Diana-alexandra Ertl practices practicing medicine in Vienna, Austria.
Ertl is highly rated in 13 conditions, according to our data. Their clinical expertise encompasses X-Linked Hypophosphatemia, Hypophosphatemia, Rickets, and Mccune-Albright Syndrome.
They are actively involved in clinical research, co-authoring 22 peer reviewed articles.
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 Diana-alexandra Ertl
Is Diana-alexandra Ertl a top-rated expert for X-Linked Hypophosphatemia?
MediFind is an objective health platform that identifies experts based on real-world data. Diana-alexandra Ertl is classified as an Distinguished expert for X-Linked Hypophosphatemia, 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 Diana-alexandra Ertl participate in research or clinical trials?
Yes. Diana-alexandra Ertl has published 22 articles and abstracts on conditions like X-Linked Hypophosphatemia. You can view a list of Diana-alexandra Ertl'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
- HypophosphatemiaErtl isDistinguished. Learn about Hypophosphatemia.
- X-Linked HypophosphatemiaErtl isDistinguished. Learn about X-Linked Hypophosphatemia.
- Advanced
- Albright's Hereditary Osteodystrophy
- Familial Hypopituitarism
- Fibrous DysplasiaErtl isAdvanced. Learn about Fibrous Dysplasia.
- Growth Hormone Deficiency (GHD)
- IntersexErtl isAdvanced. Learn about Intersex.
- MalnutritionErtl isAdvanced. Learn about Malnutrition.
- Mccune-Albright Syndrome
- Osteitis FibrosaErtl isAdvanced. Learn about Osteitis Fibrosa.
- Pseudohypoparathyroidism
- RicketsErtl isAdvanced. Learn about Rickets.
- Turner SyndromeErtl isAdvanced. Learn about Turner Syndrome.
- Experienced
- Acanthosis NigricansErtl isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaErtl isExperienced. Learn about Achondroplasia.
- AcrodysostosisErtl isExperienced. Learn about Acrodysostosis.
- Autosomal Dominant Hypocalcemia
- Brachydactyly Mononen TypeErtl isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyErtl isExperienced. Learn about Chondrodystrophy.
- Cushing's syndromeErtl isExperienced. Learn about Cushing's syndrome.
- Dysostosis PeripheralErtl isExperienced. Learn about Dysostosis Peripheral.
- Familial Hypocalciuric Hypercalcemia Type 1
- HypercalcemiaErtl isExperienced. Learn about Hypercalcemia.
- HypoparathyroidismErtl isExperienced. Learn about Hypoparathyroidism.
- Hypophosphatasia (HPP)Ertl isExperienced. Learn about Hypophosphatasia (HPP).
- HypopituitarismErtl isExperienced. Learn about Hypopituitarism.
- Milk-Alkali SyndromeErtl isExperienced. Learn about Milk-Alkali Syndrome.
- Pediatric Growth Hormone Deficiency
- Renal Hypomagnesemia Type 2Ertl isExperienced. Learn about Renal Hypomagnesemia Type 2.
- Schwartz-Jampel SyndromeErtl isExperienced. Learn about Schwartz-Jampel Syndrome.
- Sheehan SyndromeErtl isExperienced. Learn about Sheehan Syndrome.
- Short Stature (Growth Disorders)
- Small for Gestational AgeErtl isExperienced. Learn about Small for Gestational Age.
- X-Linked Spondyloepiphyseal Dysplasia Tarda