Overview
Maria Halldin practices in Huddinge, Sweden. Ms. Halldin is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. Her top areas of expertise are Primary Carnitine Deficiency, Inborn Amino Acid Metabolism Disorder, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, and Mitochondrial Trifunctional Protein Deficiency.
Her clinical research consists of co-authoring 16 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Primary Carnitine Deficiency.
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.
2 Clinical Trials
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
- Experienced
- CardiomyopathyMs. Halldin isExperienced. Learn about Cardiomyopathy.
- Inborn Amino Acid Metabolism DisorderMs. Halldin isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Lactic AcidosisMs. Halldin isExperienced. Learn about Lactic Acidosis.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency