Overview
Henrik Stranneheim practices practicing medicine in Stockholm, Sweden.
Mr. Stranneheim is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Gracile Syndrome, Inborn Renal Aminoaciduria, Lactic Acidosis, and Coenzyme Q Cytochrome C Reductase Deficiency.
He is actively involved in clinical research, co-authoring 28 peer reviewed articles.
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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.
Frequently Asked Questions about Henrik Stranneheim
Is Henrik Stranneheim a top-rated expert for Gracile Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Henrik Stranneheim is classified as an Advanced expert for Gracile Syndrome, 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 Henrik Stranneheim participate in research or clinical trials?
Yes. Henrik Stranneheim has published 28 articles and abstracts on conditions like Gracile Syndrome. You can view a list of Henrik Stranneheim'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
- Gracile SyndromeMr. Stranneheim isAdvanced. Learn about Gracile Syndrome.
- Inborn Renal AminoaciduriaMr. Stranneheim isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Lactic AcidosisMr. Stranneheim isAdvanced. Learn about Lactic Acidosis.
- Experienced
- AbetalipoproteinemiaMr. Stranneheim isExperienced. Learn about Abetalipoproteinemia.
- ChoreaMr. Stranneheim isExperienced. Learn about Chorea.
- Chorea-AcanthocytosisMr. Stranneheim isExperienced. Learn about Chorea-Acanthocytosis.
- Coenzyme Q Cytochrome C Reductase DeficiencyMr. Stranneheim isExperienced. Learn about Coenzyme Q Cytochrome C Reductase Deficiency.
- Dihydrolipoamide Dehydrogenase DeficiencyMr. Stranneheim isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Drug Induced DyskinesiaMr. Stranneheim isExperienced. Learn about Drug Induced Dyskinesia.
- Epilepsy in ChildrenMr. Stranneheim isExperienced. Learn about Epilepsy in Children.
- HemosiderosisMr. Stranneheim isExperienced. Learn about Hemosiderosis.
- HypotoniaMr. Stranneheim isExperienced. Learn about Hypotonia.
- MELAS SyndromeMr. Stranneheim isExperienced. Learn about MELAS Syndrome.
- Prader-Willi SyndromeMr. Stranneheim isExperienced. Learn about Prader-Willi Syndrome.
- Pyruvate Decarboxylase DeficiencyMr. Stranneheim isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Stranneheim isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Sensorimotor PolyneuropathyMr. Stranneheim isExperienced. Learn about Sensorimotor Polyneuropathy.
- SialadenitisMr. Stranneheim isExperienced. Learn about Sialadenitis.