Overview
Bianca Haase practices practicing medicine in Sydney, Australia.
Ms. Haase is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Hereditary Xanthinuria, Cerebral Hypoxia, Schwartz-Jampel Syndrome, and X-Linked Spondyloepiphyseal Dysplasia Tarda.
She is actively involved in clinical research, co-authoring 75 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 Bianca Haase
Is Bianca Haase a top-rated expert for Hereditary Xanthinuria?
MediFind is an objective health platform that identifies experts based on real-world data. Bianca Haase is classified as an Distinguished expert for Hereditary Xanthinuria, 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 Bianca Haase participate in research or clinical trials?
Yes. Bianca Haase has published 74 articles and abstracts on conditions like Hereditary Xanthinuria. You can view a list of Bianca Haase'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
- Hereditary XanthinuriaMs. Haase isDistinguished. Learn about Hereditary Xanthinuria.
- Experienced
- Bardet-Biedl SyndromeMs. Haase isExperienced. Learn about Bardet-Biedl Syndrome.
- Brachydactyly Mononen TypeMs. Haase isExperienced. Learn about Brachydactyly Mononen Type.
- Cerebral HypoxiaMs. Haase isExperienced. Learn about Cerebral Hypoxia.
- Childhood VolvulusMs. Haase isExperienced. Learn about Childhood Volvulus.
- ChondrodystrophyMs. Haase isExperienced. Learn about Chondrodystrophy.
- Infant Respiratory Distress SyndromeMs. Haase isExperienced. Learn about Infant Respiratory Distress Syndrome.
- Pigmented Purpuric DermatosisMs. Haase isExperienced. Learn about Pigmented Purpuric Dermatosis.
- Premature InfantMs. Haase isExperienced. Learn about Premature Infant.
- Respiratory AcidosisMs. Haase isExperienced. Learn about Respiratory Acidosis.
- Schwartz-Jampel SyndromeMs. Haase isExperienced. Learn about Schwartz-Jampel Syndrome.
- Transposition of the Great ArteriesMs. Haase isExperienced. Learn about Transposition of the Great Arteries.
- X-Linked Spondyloepiphyseal Dysplasia Tarda