Overview
Karit Reinson practices practicing medicine in Tartu, Estonia.
Reinson is highly rated in 4 conditions, according to our data. Their clinical expertise encompasses Mitochondrial Complex 1 Deficiency, Floating-Harbor Syndrome, Maternal Hyperphenylalaninemia, and Phenylketonuria (PKU).
They are actively involved in clinical research, co-authoring 38 peer reviewed articles.
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 Karit Reinson
Is Karit Reinson a top-rated expert for Mitochondrial Complex 1 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Karit Reinson is classified as an Advanced expert for Mitochondrial Complex 1 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 Karit Reinson participate in research or clinical trials?
Yes. Karit Reinson has published 38 articles and abstracts on conditions like Mitochondrial Complex 1 Deficiency. You can view a list of Karit Reinson'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
- Floating-Harbor SyndromeReinson isAdvanced. Learn about Floating-Harbor Syndrome.
- Maternal Hyperphenylalaninemia
- Mitochondrial Complex 1 Deficiency
- Phenylketonuria (PKU)Reinson isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- Angelman SyndromeReinson isExperienced. Learn about Angelman Syndrome.
- Arthrogryposis Multiplex Congenita
- Beckwith-Wiedemann SyndromeReinson isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Coffin-Lowry SyndromeReinson isExperienced. Learn about Coffin-Lowry Syndrome.
- Congenital ContracturesReinson isExperienced. Learn about Congenital Contractures.
- Drug Induced DyskinesiaReinson isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaReinson isExperienced. Learn about Dysarthria.
- EpilepsyReinson isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenReinson isExperienced. Learn about Epilepsy in Children.
- GigantismReinson isExperienced. Learn about Gigantism.
- Glutaric Acidemia Type 2Reinson isExperienced. Learn about Glutaric Acidemia Type 2.
- Hearing LossReinson isExperienced. Learn about Hearing Loss.
- HypotoniaReinson isExperienced. Learn about Hypotonia.
- Leigh SyndromeReinson isExperienced. Learn about Leigh Syndrome.
- MacroglossiaReinson isExperienced. Learn about Macroglossia.
- Movement DisordersReinson isExperienced. Learn about Movement Disorders.
- Optic Nerve AtrophyReinson isExperienced. Learn about Optic Nerve Atrophy.
- Prader-Willi SyndromeReinson isExperienced. Learn about Prader-Willi Syndrome.
- Russell-Silver DwarfismReinson isExperienced. Learn about Russell-Silver Dwarfism.
- SeizuresReinson isExperienced. Learn about Seizures.
- Sideroblastic AnemiaReinson isExperienced. Learn about Sideroblastic Anemia.
- Ventricular Septal DefectsReinson isExperienced. Learn about Ventricular Septal Defects.
- Vitamin B12 Deficiency AnemiaReinson isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Weaver SyndromeReinson isExperienced. Learn about Weaver Syndrome.