Overview
Marios Tomazou practices practicing medicine in Nicosia, Cyprus.
His clinical expertise encompasses Myotonic Dystrophy Type 2, Myotonic Dystrophy, Paramyotonia Congenita, and Familial Glucocorticoid Deficiency.
He is actively involved in clinical research, co-authoring 32 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 Marios Tomazou
Is Marios Tomazou a top-rated expert for Myotonic Dystrophy Type 2?
MediFind is an objective health platform that identifies experts based on real-world data. Marios Tomazou is classified as an Experienced expert for Myotonic Dystrophy Type 2, 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 Marios Tomazou participate in research or clinical trials?
Yes. Marios Tomazou has published 32 articles and abstracts on conditions like Myotonic Dystrophy Type 2. You can view a list of Marios Tomazou'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
- Experienced
- Congenital Hemolytic AnemiaMr. Tomazou isExperienced. Learn about Congenital Hemolytic Anemia.
- Congenital Myasthenic SyndromeMr. Tomazou isExperienced. Learn about Congenital Myasthenic Syndrome.
- Dihydropyrimidine Dehydrogenase Deficiency
- Drug Induced DyskinesiaMr. Tomazou isExperienced. Learn about Drug Induced Dyskinesia.
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Familial Glucocorticoid DeficiencyMr. Tomazou isExperienced. Learn about Familial Glucocorticoid Deficiency.
- Farber LipogranulomatosisMr. Tomazou isExperienced. Learn about Farber Lipogranulomatosis.
- HemoglobinopathyMr. Tomazou isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaMr. Tomazou isExperienced. Learn about Hemolytic Anemia.
- Limb-Girdle Muscular DystrophyMr. Tomazou isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Myotonic DystrophyMr. Tomazou isExperienced. Learn about Myotonic Dystrophy.
- Myotonic Dystrophy Type 2Mr. Tomazou isExperienced. Learn about Myotonic Dystrophy Type 2.
- Paramyotonia CongenitaMr. Tomazou isExperienced. Learn about Paramyotonia Congenita.
- Prader-Willi SyndromeMr. Tomazou isExperienced. Learn about Prader-Willi Syndrome.
- Precocious PubertyMr. Tomazou isExperienced. Learn about Precocious Puberty.
- ThalassemiaMr. Tomazou isExperienced. Learn about Thalassemia.