Overview
Aysylu Murtazina practices practicing medicine in Moscow, Russian Federation.
Murtazina is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Hereditary Multiple Osteochondromas, Osteochondroma, Marden-Walker Syndrome, and Metachondromatosis.
They are actively involved in clinical research, co-authoring 40 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 Aysylu F. Murtazina
Is Aysylu F. Murtazina a top-rated expert for Hereditary Multiple Osteochondromas?
MediFind is an objective health platform that identifies experts based on real-world data. Aysylu F. Murtazina is classified as an Advanced expert for Hereditary Multiple Osteochondromas, 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 Aysylu F. Murtazina participate in research or clinical trials?
Yes. Aysylu F. Murtazina has published 40 articles and abstracts on conditions like Hereditary Multiple Osteochondromas. You can view a list of Aysylu F. Murtazina'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
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Hereditary Multiple Osteochondromas
- Marden-Walker SyndromeMurtazina isAdvanced. Learn about Marden-Walker Syndrome.
- MetachondromatosisMurtazina isAdvanced. Learn about Metachondromatosis.
- OsteochondromaMurtazina isAdvanced. Learn about Osteochondroma.
- Experienced
- Adenylosuccinate Lyase DeficiencyMurtazina isExperienced. Learn about Adenylosuccinate Lyase Deficiency.
- Amyotonia CongenitaMurtazina isExperienced. Learn about Amyotonia Congenita.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Arthrogryposis Multiplex CongenitaMurtazina isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Becker Muscular DystrophyMurtazina isExperienced. Learn about Becker Muscular Dystrophy.
- Charcot-Marie-Tooth DiseaseMurtazina isExperienced. Learn about Charcot-Marie-Tooth Disease.
- Collagen VI-Related MyopathyMurtazina isExperienced. Learn about Collagen VI-Related Myopathy.
- Congenital ContracturesMurtazina isExperienced. Learn about Congenital Contractures.
- 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.
- Distal ArthrogryposisMurtazina isExperienced. Learn about Distal Arthrogryposis.
- Distal Arthrogryposis Type 6Murtazina isExperienced. Learn about Distal Arthrogryposis Type 6.
- Duchenne Muscular DystrophyMurtazina isExperienced. Learn about Duchenne Muscular Dystrophy.
- EncephaloceleMurtazina isExperienced. Learn about Encephalocele.
- Facial ParalysisMurtazina isExperienced. Learn about Facial Paralysis.
- HypotoniaMurtazina isExperienced. Learn about Hypotonia.
- Inclusion Body Myopathy 2Murtazina isExperienced. Learn about Inclusion Body Myopathy 2.
- LaryngomalaciaMurtazina isExperienced. Learn about Laryngomalacia.
- Leber Hereditary Optic Neuropathy (LHON)
- Leigh SyndromeMurtazina isExperienced. Learn about Leigh Syndrome.
- Limb-Girdle Muscular DystrophyMurtazina isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- MELAS SyndromeMurtazina isExperienced. Learn about MELAS Syndrome.
- Moebius SyndromeMurtazina isExperienced. Learn about Moebius Syndrome.
- Myotonia CongenitaMurtazina isExperienced. Learn about Myotonia Congenita.
- Paramyotonia CongenitaMurtazina isExperienced. Learn about Paramyotonia Congenita.
- Potassium-Aggravated MyotoniaMurtazina isExperienced. Learn about Potassium-Aggravated Myotonia.
- Primary Lateral SclerosisMurtazina isExperienced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)Murtazina isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- Spinal Muscular Atrophy Type 2Murtazina isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Murtazina isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Tubular Aggregate MyopathyMurtazina isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Dominant Scapuloperoneal Myopathy
- X-Linked HypophosphatemiaMurtazina isExperienced. Learn about X-Linked Hypophosphatemia.
- X-Linked Myotubular MyopathyMurtazina isExperienced. Learn about X-Linked Myotubular Myopathy.