Overview
Shanti Balasubramaniam practices practicing medicine in Subiaco, Australia.
Ms. Balasubramaniam is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Multiple Carboxylase Deficiency, Holocarboxylase Synthetase Deficiency, Cutis Laxa, and Gerodermia Osteodysplastica.
She is actively involved in clinical research, co-authoring 53 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 Shanti D. Balasubramaniam
Is Shanti D. Balasubramaniam a top-rated expert for Multiple Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Shanti D. Balasubramaniam is classified as an Distinguished 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 Shanti D. Balasubramaniam participate in research or clinical trials?
Yes. Shanti D. Balasubramaniam has published 53 articles and abstracts on conditions like Multiple Carboxylase Deficiency. You can view a list of Shanti D. Balasubramaniam'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
- Distinguished
- Holocarboxylase Synthetase DeficiencyMs. Balasubramaniam isDistinguished. Learn about Holocarboxylase Synthetase Deficiency.
- Multiple Carboxylase DeficiencyMs. Balasubramaniam isDistinguished. Learn about Multiple Carboxylase Deficiency.
- Advanced
- Cutis LaxaMs. Balasubramaniam isAdvanced. Learn about Cutis Laxa.
- Fumarase DeficiencyMs. Balasubramaniam isAdvanced. Learn about Fumarase Deficiency.
- Gerodermia OsteodysplasticaMs. Balasubramaniam isAdvanced. Learn about Gerodermia Osteodysplastica.
- Glycine EncephalopathyMs. Balasubramaniam isAdvanced. Learn about Glycine Encephalopathy.
- Leigh SyndromeMs. Balasubramaniam isAdvanced. Learn about Leigh Syndrome.
- Mohr-Tranebjaerg SyndromeMs. Balasubramaniam isAdvanced. Learn about Mohr-Tranebjaerg Syndrome.
- Vici SyndromeMs. Balasubramaniam isAdvanced. Learn about Vici Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeMs. Balasubramaniam isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Adenylosuccinate Lyase DeficiencyMs. Balasubramaniam isExperienced. Learn about Adenylosuccinate Lyase Deficiency.
- Barth SyndromeMs. Balasubramaniam isExperienced. Learn about Barth Syndrome.
- CardiomyopathyMs. Balasubramaniam isExperienced. Learn about Cardiomyopathy.
- Cortical DysplasiaMs. Balasubramaniam isExperienced. Learn about Cortical Dysplasia.
- Cytochrome C Oxidase DeficiencyMs. Balasubramaniam isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Delayed GrowthMs. Balasubramaniam isExperienced. Learn about Delayed Growth.
- Diabetic KetoacidosisMs. Balasubramaniam isExperienced. Learn about Diabetic Ketoacidosis.
- Drug Induced DyskinesiaMs. Balasubramaniam isExperienced. Learn about Drug Induced Dyskinesia.
- Hearing LossMs. Balasubramaniam isExperienced. Learn about Hearing Loss.
- Human Papillomavirus InfectionMs. Balasubramaniam isExperienced. Learn about Human Papillomavirus Infection.
- Hypomelanotic DisorderMs. Balasubramaniam isExperienced. Learn about Hypomelanotic Disorder.
- HypotoniaMs. Balasubramaniam isExperienced. Learn about Hypotonia.
- Lactic AcidosisMs. Balasubramaniam isExperienced. Learn about Lactic Acidosis.
- Low Blood SugarMs. Balasubramaniam isExperienced. Learn about Low Blood Sugar.
- Maple Syrup Urine DiseaseMs. Balasubramaniam isExperienced. Learn about Maple Syrup Urine Disease.
- MicrocephalyMs. Balasubramaniam isExperienced. Learn about Microcephaly.
- Microcephaly Deafness SyndromeMs. Balasubramaniam isExperienced. Learn about Microcephaly Deafness Syndrome.
- Mitochondrial Complex V DeficiencyMs. Balasubramaniam isExperienced. Learn about Mitochondrial Complex V Deficiency.
- Mucopolysaccharidoses (MPS)Ms. Balasubramaniam isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Myofibrillar MyopathyMs. Balasubramaniam isExperienced. Learn about Myofibrillar Myopathy.
- Niemann-Pick DiseaseMs. Balasubramaniam isExperienced. Learn about Niemann-Pick Disease.
- Optic Nerve AtrophyMs. Balasubramaniam isExperienced. Learn about Optic Nerve Atrophy.
- OsteopetrosisMs. Balasubramaniam isExperienced. Learn about Osteopetrosis.
- Osteosclerosis Autosomal DominantMs. Balasubramaniam isExperienced. Learn about Osteosclerosis Autosomal Dominant.
- PMM2-Congenital Disorder of GlycosylationMs. Balasubramaniam isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Pyridoxine DeficiencyMs. Balasubramaniam isExperienced. Learn about Pyridoxine Deficiency.
- RhabdomyolysisMs. Balasubramaniam isExperienced. Learn about Rhabdomyolysis.
- SeizuresMs. Balasubramaniam isExperienced. Learn about Seizures.
- SpasticityMs. Balasubramaniam isExperienced. Learn about Spasticity.
- Urea Cycle Disorders (UCD)Ms. Balasubramaniam isExperienced. Learn about Urea Cycle Disorders (UCD).