Overview
Rose Maase practices practicing medicine in Bilthoven, Netherlands.
Ms. Maase is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Primary Carnitine Deficiency, Protein Deficiency, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, and Mitochondrial Trifunctional Protein Deficiency.
She is actively involved in clinical research, co-authoring 14 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 Rose E. Maase
Is Rose E. Maase a top-rated expert for Primary Carnitine Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Rose E. Maase is classified as an Advanced expert for Primary Carnitine 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 Rose E. Maase participate in research or clinical trials?
Yes. Rose E. Maase has published 14 articles and abstracts on conditions like Primary Carnitine Deficiency. You can view a list of Rose E. Maase'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
- Advanced
- Primary Carnitine DeficiencyMs. Maase isAdvanced. Learn about Primary Carnitine Deficiency.
- Experienced
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseMs. Maase isExperienced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaMs. Maase isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Trifunctional Protein Deficiency
- Newborn Low Blood SugarMs. Maase isExperienced. Learn about Newborn Low Blood Sugar.
- Propionic AcidemiaMs. Maase isExperienced. Learn about Propionic Acidemia.
- Protein DeficiencyMs. Maase isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Maase isExperienced. Learn about Rhabdomyolysis.
- Tyrosinemia Type 1Ms. Maase isExperienced. Learn about Tyrosinemia Type 1.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Vitamin B12 DeficiencyMs. Maase isExperienced. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Maase isExperienced. Learn about Vitamin B12 Deficiency Anemia.