Overview
Sabine Scholl-Burgi practices in Innsbruck, Austria. Ms. Scholl-Burgi is rated as an Experienced expert by MediFind in the treatment of X-Linked Spondyloepiphyseal Dysplasia Tarda. Her top areas of expertise are Classic Galactosemia, Inborn Amino Acid Metabolism Disorder, Propionic Acidemia, Hepato-Pancreato-Biliary Surgery, and Liver Transplant.
Her clinical research consists of co-authoring 124 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of X-Linked Spondyloepiphyseal Dysplasia Tarda.
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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.
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
- Classic GalactosemiaMs. Scholl-Burgi isDistinguished. Learn about Classic Galactosemia.
- GalactosemiaMs. Scholl-Burgi isDistinguished. Learn about Galactosemia.
- Hyaline Fibromatosis SyndromeMs. Scholl-Burgi isDistinguished. Learn about Hyaline Fibromatosis Syndrome.
- Inborn Amino Acid Metabolism DisorderMs. Scholl-Burgi isDistinguished. Learn about Inborn Amino Acid Metabolism Disorder.
- Propionic AcidemiaMs. Scholl-Burgi isDistinguished. Learn about Propionic Acidemia.
- Urea Cycle Disorders (UCD)Ms. Scholl-Burgi isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Argininosuccinic AciduriaMs. Scholl-Burgi isAdvanced. Learn about Argininosuccinic Aciduria.
- Familial HypercholesterolemiaMs. Scholl-Burgi isAdvanced. Learn about Familial Hypercholesterolemia.
- Galactokinase DeficiencyMs. Scholl-Burgi isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Scholl-Burgi isAdvanced. Learn about Galactose Epimerase Deficiency.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaMs. Scholl-Burgi isAdvanced. Learn about Methylmalonic Acidemia.
- Experienced
- Arginase DeficiencyMs. Scholl-Burgi isExperienced. Learn about Arginase Deficiency.
- Brachydactyly Mononen TypeMs. Scholl-Burgi isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 DeficiencyMs. Scholl-Burgi isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- CardiomyopathyMs. Scholl-Burgi isExperienced. Learn about Cardiomyopathy.
- ChondrodystrophyMs. Scholl-Burgi isExperienced. Learn about Chondrodystrophy.
- Congenital Heart Disease (CHD)Ms. Scholl-Burgi isExperienced. Learn about Congenital Heart Disease (CHD).