Overview
Vykuntaraju Gowda practices in Bengaluru, India. Gowda is highly rated in 76 conditions, according to our data. Their top areas of expertise are Multiple Carboxylase Deficiency, Biotinidase Deficiency, Riboflavin Transporter Deficiency Neuronopathy, and West Syndrome.
Their clinical research consists of co-authoring 212 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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 Vykuntaraju K. Gowda
Is Vykuntaraju K. Gowda a top-rated expert for Multiple Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Vykuntaraju K. Gowda is classified as an Elite expert for Multiple Carboxylase 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 Vykuntaraju K. Gowda participate in research or clinical trials?
Yes. Vykuntaraju K. Gowda has published 212 articles and abstracts on conditions like Multiple Carboxylase Deficiency. You can view a list of Vykuntaraju K. Gowda'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
- Elite
- Biotinidase Deficiency
- Multiple Carboxylase Deficiency
- Riboflavin Transporter Deficiency Neuronopathy
- Distinguished
- Absence SeizureGowda isDistinguished. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeGowda isDistinguished. Learn about Achalasia Microcephaly Syndrome.
- Aicardi-Goutieres SyndromeGowda isDistinguished. Learn about Aicardi-Goutieres Syndrome.
- CACH SyndromeGowda isDistinguished. Learn about CACH Syndrome.
- Canavan DiseaseGowda isDistinguished. Learn about Canavan Disease.
- Cortical DysplasiaGowda isDistinguished. Learn about Cortical Dysplasia.
- Advanced
- Acute Flaccid Myelitis (AFM)
- Andermann SyndromeGowda isAdvanced. Learn about Andermann Syndrome.
- AnhidrosisGowda isAdvanced. Learn about Anhidrosis.
- Anti-NMDA Receptor Encephalitis
- CalcinosisGowda isAdvanced. Learn about Calcinosis.
- Cerebelloolivary Atrophy
- Experienced
- Aase SyndromeGowda isExperienced. Learn about Aase Syndrome.
- Acute Cerebellar AtaxiaGowda isExperienced. Learn about Acute Cerebellar Ataxia.
- Acute Intermittent PorphyriaGowda isExperienced. Learn about Acute Intermittent Porphyria.
- ADULT SyndromeGowda isExperienced. Learn about ADULT Syndrome.
- Alpha MannosidosisGowda isExperienced. Learn about Alpha Mannosidosis.
- Alternating Hemiplegia of Childhood