Overview
Zoi Kontogeorgiou practices in Athens, Greece. Ms. Kontogeorgiou is rated as an Experienced expert by MediFind in the treatment of Continuous Muscle Fiber Activity Hereditary. Her top areas of expertise are Acute Cerebellar Ataxia, Charcot-Marie-Tooth Disease, Spinocerebellar Ataxia Type 27, and Isaacs' Syndrome.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Continuous Muscle Fiber Activity Hereditary.
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.
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
- Acute Cerebellar AtaxiaMs. Kontogeorgiou isAdvanced. Learn about Acute Cerebellar Ataxia.
- Charcot-Marie-Tooth DiseaseMs. Kontogeorgiou isAdvanced. Learn about Charcot-Marie-Tooth Disease.
- Experienced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Cardiac AmyloidosisMs. Kontogeorgiou isExperienced. Learn about Cardiac Amyloidosis.
- Continuous Muscle Fiber Activity HereditaryMs. Kontogeorgiou isExperienced. Learn about Continuous Muscle Fiber Activity Hereditary.
- Drug Induced DyskinesiaMs. Kontogeorgiou isExperienced. Learn about Drug Induced Dyskinesia.
- Familial Transthyretin AmyloidosisMs. Kontogeorgiou isExperienced. Learn about Familial Transthyretin Amyloidosis.
- Hereditary AtaxiaMs. Kontogeorgiou isExperienced. Learn about Hereditary Ataxia.