Overview
Aysylu Murtazina practices in Moscow, Russian Federation. Murtazina is rated as an Experienced expert by MediFind in the treatment of Collagen VI-Related Myopathy. Their top areas of expertise are Hereditary Multiple Osteochondromas, Osteochondroma, Metachondromatosis, and Facioscapulohumeral Muscular Dystrophy (FSHD).
Their clinical research consists of co-authoring 26 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of Collagen VI-Related Myopathy.
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
- Hereditary Multiple Osteochondromas
- MetachondromatosisMurtazina isAdvanced. Learn about Metachondromatosis.
- OsteochondromaMurtazina isAdvanced. Learn about Osteochondroma.
- Experienced
- Amyotonia CongenitaMurtazina isExperienced. Learn about Amyotonia Congenita.
- Collagen VI-Related MyopathyMurtazina isExperienced. Learn about Collagen VI-Related Myopathy.
- Congenital Fiber-Type DisproportionMurtazina isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Congenital Myasthenic SyndromeMurtazina isExperienced. Learn about Congenital Myasthenic Syndrome.
- Cytochrome C Oxidase DeficiencyMurtazina isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Delta-SarcoglycanopathyMurtazina isExperienced. Learn about Delta-Sarcoglycanopathy.