Overview
Gillian Riordan practices practicing medicine in Cape Town, South Africa.
Ms. Riordan is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Lactic Acidosis, Mohr-Tranebjaerg Syndrome, Riboflavin Transporter Deficiency Neuronopathy, and Myoclonic Epilepsy.
She is actively involved in clinical research, co-authoring 16 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 Gillian T. Riordan
Is Gillian T. Riordan a top-rated expert for Lactic Acidosis?
MediFind is an objective health platform that identifies experts based on real-world data. Gillian T. Riordan is classified as an Advanced expert for Lactic Acidosis, 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 Gillian T. Riordan participate in research or clinical trials?
Yes. Gillian T. Riordan has published 16 articles and abstracts on conditions like Lactic Acidosis. You can view a list of Gillian T. Riordan'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
- Lactic AcidosisMs. Riordan isAdvanced. Learn about Lactic Acidosis.
- Mohr-Tranebjaerg SyndromeMs. Riordan isAdvanced. Learn about Mohr-Tranebjaerg Syndrome.
- Riboflavin Transporter Deficiency Neuronopathy
- Experienced
- Dentatorubral-Pallidoluysian AtrophyMs. Riordan isExperienced. Learn about Dentatorubral-Pallidoluysian Atrophy.
- Epilepsy in ChildrenMs. Riordan isExperienced. Learn about Epilepsy in Children.
- Hearing LossMs. Riordan isExperienced. Learn about Hearing Loss.
- HypotoniaMs. Riordan isExperienced. Learn about Hypotonia.
- Lafora DiseaseMs. Riordan isExperienced. Learn about Lafora Disease.
- Leber Hereditary Optic Neuropathy (LHON)Ms. Riordan isExperienced. Learn about Leber Hereditary Optic Neuropathy (LHON).
- Leigh SyndromeMs. Riordan isExperienced. Learn about Leigh Syndrome.
- MELAS SyndromeMs. Riordan isExperienced. Learn about MELAS Syndrome.
- Mitochondrial Complex 1 DeficiencyMs. Riordan isExperienced. Learn about Mitochondrial Complex 1 Deficiency.
- Myoclonic EpilepsyMs. Riordan isExperienced. Learn about Myoclonic Epilepsy.
- Opsoclonus-Myoclonus SyndromeMs. Riordan isExperienced. Learn about Opsoclonus-Myoclonus Syndrome.
- Optic Nerve AtrophyMs. Riordan isExperienced. Learn about Optic Nerve Atrophy.
- Primary Lateral SclerosisMs. Riordan isExperienced. Learn about Primary Lateral Sclerosis.
- Progressive Myoclonic EpilepsyMs. Riordan isExperienced. Learn about Progressive Myoclonic Epilepsy.
- Pyruvate Decarboxylase DeficiencyMs. Riordan isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Riordan isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Unverricht-Lundborg SyndromeMs. Riordan isExperienced. Learn about Unverricht-Lundborg Syndrome.