Overview
Galina Baydakova practices practicing medicine in Moscow, Russian Federation.
Ms. Baydakova is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Farber Lipogranulomatosis, Parkinson's Disease, Gaucher Disease, and Movement Disorders.
She is actively involved in clinical research, co-authoring 50 peer reviewed articles.
Gender
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 Galina V. Baydakova
Is Galina V. Baydakova a top-rated expert for Farber Lipogranulomatosis?
MediFind is an objective health platform that identifies experts based on real-world data. Galina V. Baydakova is classified as an Advanced expert for Farber Lipogranulomatosis, 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 Galina V. Baydakova participate in research or clinical trials?
Yes. Galina V. Baydakova has published 50 articles and abstracts on conditions like Farber Lipogranulomatosis. You can view a list of Galina V. Baydakova'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
- Brachydactyly Mononen TypeMs. Baydakova isAdvanced. Learn about Brachydactyly Mononen Type.
- Farber LipogranulomatosisMs. Baydakova isAdvanced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseMs. Baydakova isAdvanced. Learn about Gaucher Disease.
- Movement DisordersMs. Baydakova isAdvanced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)Ms. Baydakova isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Niemann-Pick DiseaseMs. Baydakova isAdvanced. Learn about Niemann-Pick Disease.
- Parkinson's DiseaseMs. Baydakova isAdvanced. Learn about Parkinson's Disease.
- Experienced
- Achalasia Microcephaly SyndromeMs. Baydakova isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Baydakova isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Alagille SyndromeMs. Baydakova isExperienced. Learn about Alagille Syndrome.
- AlkaptonuriaMs. Baydakova isExperienced. Learn about Alkaptonuria.
- Alpha MannosidosisMs. Baydakova isExperienced. Learn about Alpha Mannosidosis.
- Autosomal Recessive Primary MicrocephalyMs. Baydakova isExperienced. Learn about Autosomal Recessive Primary Microcephaly.
- C SyndromeMs. Baydakova isExperienced. Learn about C Syndrome.
- CACH SyndromeMs. Baydakova isExperienced. Learn about CACH Syndrome.
- Corpus Callosum AgenesisMs. Baydakova isExperienced. Learn about Corpus Callosum Agenesis.
- Fabry DiseaseMs. Baydakova isExperienced. Learn about Fabry Disease.
- Familial DysautonomiaMs. Baydakova isExperienced. Learn about Familial Dysautonomia.
- GangliosidosisMs. Baydakova isExperienced. Learn about Gangliosidosis.
- Glutaric Acidemia Type 1Ms. Baydakova isExperienced. Learn about Glutaric Acidemia Type 1.
- GTP Cyclohydrolase 1 DeficiencyMs. Baydakova isExperienced. Learn about GTP Cyclohydrolase 1 Deficiency.
- HistiocytosisMs. Baydakova isExperienced. Learn about Histiocytosis.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseMs. Baydakova isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaMs. Baydakova isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Metachromatic LeukodystrophyMs. Baydakova isExperienced. Learn about Metachromatic Leukodystrophy.
- MicrocephalyMs. Baydakova isExperienced. Learn about Microcephaly.
- Mucolipidosis 3Ms. Baydakova isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Baydakova isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple System AtrophyMs. Baydakova isExperienced. Learn about Multiple System Atrophy.
- Neurotoxicity SyndromesMs. Baydakova isExperienced. Learn about Neurotoxicity Syndromes.
- Non-Langerhans-Cell HistiocytosisMs. Baydakova isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- OchronosisMs. Baydakova isExperienced. Learn about Ochronosis.
- Phenylketonuria (PKU)Ms. Baydakova isExperienced. Learn about Phenylketonuria (PKU).
- Progressive Familial Intrahepatic Cholestasis Type 1
- Propionic AcidemiaMs. Baydakova isExperienced. Learn about Propionic Acidemia.
- Protein DeficiencyMs. Baydakova isExperienced. Learn about Protein Deficiency.
- ReticulohistiocytomaMs. Baydakova isExperienced. Learn about Reticulohistiocytoma.
- SialidosisMs. Baydakova isExperienced. Learn about Sialidosis.
- Tay-Sachs DiseaseMs. Baydakova isExperienced. Learn about Tay-Sachs Disease.
- Tyrosinemia Type 1Ms. Baydakova isExperienced. Learn about Tyrosinemia Type 1.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency