Overview
Muralidharan Nair practices practicing medicine in Thiruvananthapuram, India.
Nair is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Beta-Ketothiolase Deficiency, Congenital Myasthenic Syndrome, Myoglobinuria Recurrent, Papular Mucinosis, and Thymectomy.
They are actively involved in clinical research, co-authoring 38 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 Muralidharan D. Nair
Is Muralidharan D. Nair a top-rated expert for Beta-Ketothiolase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Muralidharan D. Nair is classified as an Advanced expert for Beta-Ketothiolase Deficiency, 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 Muralidharan D. Nair participate in research or clinical trials?
Yes. Muralidharan D. Nair has published 38 articles and abstracts on conditions like Beta-Ketothiolase Deficiency. You can view a list of Muralidharan D. Nair'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
- Beta-Ketothiolase Deficiency
- Congenital Myasthenic Syndrome
- Experienced
- Brown SyndromeNair isExperienced. Learn about Brown Syndrome.
- CACH SyndromeNair isExperienced. Learn about CACH Syndrome.
- Central Core DiseaseNair isExperienced. Learn about Central Core Disease.
- Congenital Fiber-Type Disproportion
- Drug Induced DyskinesiaNair isExperienced. Learn about Drug Induced Dyskinesia.
- EclampsiaNair isExperienced. Learn about Eclampsia.
- Kearns-Sayre SyndromeNair isExperienced. Learn about Kearns-Sayre Syndrome.
- LeukodystrophyNair isExperienced. Learn about Leukodystrophy.
- Metachromatic Leukodystrophy
- MyelitisNair isExperienced. Learn about Myelitis.
- Myoglobinuria RecurrentNair isExperienced. Learn about Myoglobinuria Recurrent.
- MyositisNair isExperienced. Learn about Myositis.
- NeurosarcoidosisNair isExperienced. Learn about Neurosarcoidosis.
- Papular MucinosisNair isExperienced. Learn about Papular Mucinosis.
- Photosensitive EpilepsyNair isExperienced. Learn about Photosensitive Epilepsy.
- Progressive External Ophthalmoplegia
- Relapsing Multiple Sclerosis (RMS)
- RhabdomyolysisNair isExperienced. Learn about Rhabdomyolysis.
- ScleromyxedemaNair isExperienced. Learn about Scleromyxedema.
- SeizuresNair isExperienced. Learn about Seizures.
- Status EpilepticusNair isExperienced. Learn about Status Epilepticus.
- ThymectomyNair isExperienced. Learn about Thymectomy.
- Tubular Aggregate MyopathyNair isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular Myopathy