Overview
Janne Purhonen practices practicing medicine in Helsinki, Finland.
Ms. Purhonen is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Coenzyme Q Cytochrome C Reductase Deficiency, Gracile Syndrome, Inborn Renal Aminoaciduria, and Mitochondrial Complex 3 Deficiency.
She is actively involved in clinical research, co-authoring 16 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 Janne Purhonen
Is Janne Purhonen a top-rated expert for Coenzyme Q Cytochrome C Reductase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Janne Purhonen is classified as an Elite expert for Coenzyme Q Cytochrome C Reductase 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 Janne Purhonen participate in research or clinical trials?
Yes. Janne Purhonen has published 16 articles and abstracts on conditions like Coenzyme Q Cytochrome C Reductase Deficiency. You can view a list of Janne Purhonen'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
- Elite
- Coenzyme Q Cytochrome C Reductase Deficiency
- Distinguished
- Gracile SyndromeMs. Purhonen isDistinguished. Learn about Gracile Syndrome.
- Inborn Renal AminoaciduriaMs. Purhonen isDistinguished. Learn about Inborn Renal Aminoaciduria.
- Mitochondrial Complex 3 DeficiencyMs. Purhonen isDistinguished. Learn about Mitochondrial Complex 3 Deficiency.
- Advanced
- HemosiderosisMs. Purhonen isAdvanced. Learn about Hemosiderosis.
- Lactic AcidosisMs. Purhonen isAdvanced. Learn about Lactic Acidosis.
- Experienced
- Bile Duct ObstructionMs. Purhonen isExperienced. Learn about Bile Duct Obstruction.
- CholestasisMs. Purhonen isExperienced. Learn about Cholestasis.
- Intrauterine Growth RestrictionMs. Purhonen isExperienced. Learn about Intrauterine Growth Restriction.
- MELAS SyndromeMs. Purhonen isExperienced. Learn about MELAS Syndrome.
- ProgeriaMs. Purhonen isExperienced. Learn about Progeria.