Overview
Emma Glamuzina practices practicing medicine in Auckland, New Zealand.
Ms. Glamuzina is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Holocarboxylase Synthetase Deficiency, Carnitine-Acylcarnitine Translocase Deficiency, Beriberi, and Isovaleric Acidemia.
She is actively involved in clinical research, co-authoring 29 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 Emma E. Glamuzina
Is Emma E. Glamuzina a top-rated expert for Holocarboxylase Synthetase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Emma E. Glamuzina is classified as an Advanced expert for Holocarboxylase Synthetase 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 Emma E. Glamuzina participate in research or clinical trials?
Yes. Emma E. Glamuzina has published 29 articles and abstracts on conditions like Holocarboxylase Synthetase Deficiency. You can view a list of Emma E. Glamuzina'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
- Carnitine-Acylcarnitine Translocase Deficiency
- Holocarboxylase Synthetase DeficiencyMs. Glamuzina isAdvanced. Learn about Holocarboxylase Synthetase Deficiency.
- Experienced
- AlbinismMs. Glamuzina isExperienced. Learn about Albinism.
- Argininosuccinic AciduriaMs. Glamuzina isExperienced. Learn about Argininosuccinic Aciduria.
- BeriberiMs. Glamuzina isExperienced. Learn about Beriberi.
- EpilepsyMs. Glamuzina isExperienced. Learn about Epilepsy.
- Isovaleric AcidemiaMs. Glamuzina isExperienced. Learn about Isovaleric Acidemia.
- JaundiceMs. Glamuzina isExperienced. Learn about Jaundice.
- Leigh SyndromeMs. Glamuzina isExperienced. Learn about Leigh Syndrome.
- LeukodystrophyMs. Glamuzina isExperienced. Learn about Leukodystrophy.
- Mitochondrial Complex V DeficiencyMs. Glamuzina isExperienced. Learn about Mitochondrial Complex V Deficiency.
- Multiple Carboxylase DeficiencyMs. Glamuzina isExperienced. Learn about Multiple Carboxylase Deficiency.
- Myofibrillar MyopathyMs. Glamuzina isExperienced. Learn about Myofibrillar Myopathy.
- Neuronal Intranuclear Inclusion Disease (NIID)
- Urea Cycle Disorders (UCD)Ms. Glamuzina isExperienced. Learn about Urea Cycle Disorders (UCD).