Overview
Lock-hock Ngu practices practicing medicine in Kuala Lumpur, Malaysia.
Ngu is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Hypotonia, Inborn Amino Acid Metabolism Disorder, and Glycogen Storage Disease Type 3.
They are actively involved in clinical research, co-authoring 25 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 Lock-hock H. Ngu
Is Lock-hock H. Ngu a top-rated expert for Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Lock-hock H. Ngu is classified as an Advanced expert for Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), 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 Lock-hock H. Ngu participate in research or clinical trials?
Yes. Lock-hock H. Ngu has published 25 articles and abstracts on conditions like Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). You can view a list of Lock-hock H. Ngu'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
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Experienced
- AnaphylaxisNgu isExperienced. Learn about Anaphylaxis.
- Cutis LaxaNgu isExperienced. Learn about Cutis Laxa.
- Glycogen Storage Disease Type 3
- HypotoniaNgu isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism Disorder
- Maple Syrup Urine DiseaseNgu isExperienced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaNgu isExperienced. Learn about Methylmalonic Acidemia.
- Urea Cycle Disorders (UCD)
- Waardenburg SyndromeNgu isExperienced. Learn about Waardenburg Syndrome.
- Waardenburg Syndrome Type 1
- Xeroderma PigmentosumNgu isExperienced. Learn about Xeroderma Pigmentosum.